(2-Iodophenyl)Methanol

Fengxi Chemical

Specifications

HS Code	895600
Chemical Formula	C7H7IO
Molar Mass	220.034 g/mol
Appearance	Solid
Melting Point	N/A (no common data found, needs further research)
Boiling Point	N/A (no common data found, needs further research)
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in some organic solvents like ethanol, chloroform
Density	N/A (no common data found, needs further research)
Flash Point	N/A (no common data found, needs further research)
Stability	Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula	C7H7IO
Molar Mass	220.03 g/mol
Appearance	Solid
Melting Point	Typically in a certain range (exact value may vary based on purity)
Boiling Point	Would require specific experimental determination
Solubility In Water	Low solubility
Solubility In Organic Solvents	Moderate to good solubility in common organic solvents like ethanol, dichloromethane
Density	Data would depend on experimental conditions and purity
Flash Point	Requires experimental determination
Hazard Class	May be harmful if swallowed, inhaled or in contact with skin; details vary by jurisdiction
Chemical Formula	C7H7IO
Molecular Weight	234.03
Appearance	Solid
Melting Point	63 - 67 °C
Boiling Point	277.6 °C at 760 mmHg
Density	1.859 g/cm³
Flash Point	121.7 °C
Solubility	Soluble in organic solvents
Refractive Index	1.643
Cas Number	67099-86-9

As an accredited (2-Iodophenyl)Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	(2 - iodophenyl)methanol: Packed in 100 - gram bottles for secure storage and transport.
Storage	(2 - iodophenyl)methanol should be stored in a cool, dry place away from heat and ignition sources. Keep it in a tightly - sealed container to prevent moisture absorption and evaporation. Store it separately from oxidizing agents and incompatible substances to avoid potential chemical reactions. Preferably, store it in a dedicated chemical storage area following safety regulations.
Shipping	(2 - iodophenyl)methanol is a chemical that requires careful shipping. It should be packaged in a well - sealed, appropriate container to prevent leakage. Shipments must comply with regulations for hazardous or special chemicals, ensuring safe transit.

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General Information

Historical Development

(2-Iodophenyl) methanol, the development process of this substance is really impressive. In the past, chemical sages explored the mysteries of matter and worked tirelessly in the field of organic synthesis. Although the conditions were difficult at that time, everyone was determined. After many attempts, the fusion of iodine-containing compounds and alcohols at the beginning was quite laborious. However, the wise man is good at thinking, and he is clever at changing the reaction conditions and adjusting the ratio of raw materials. After countless days and nights, he finally got the method of synthesizing (2-iodophenyl) methanol. This process is like clearing the clouds to see the sun, and giving birth to hope in hardships. Since its advent, it has emerged in the fields of medicine, materials and other fields, opened a new chapter of application, and laid the foundation for the development of chemistry in later generations. It is really a brilliant stroke in the history of chemistry.

Product Overview

(2-Iodophenyl) methanol is an organic compound. Its shape or crystalline body, color or white, with specific rationalization. In the field of organic synthesis, this compound has a wide range of uses.
Its structure is unique, the iodine atom is connected to the benzene ring, and the methanol group is also connected to the benzene ring. Due to the large atomic weight of iodine, it has strong electron absorption, which affects the electron cloud distribution of molecules, making the compound have special reactivity. Methanol groups can participate in a variety of reactions, such as esterification, oxidation, etc.
Preparation of this compound, often with a specific reaction path. Through the halogenation of the benzene ring, iodine atoms are introduced, and then through specific steps, methanol groups are connected. When synthesizing, it is necessary to pay attention to the reaction conditions, such as temperature, solvent, catalyst, etc., which will affect the purity and yield of the product.
(2-iodophenyl) methanol has potential applications in many fields such as medicine and materials science. It can be used as an intermediate in pharmaceutical synthesis to help create new drugs; in material synthesis, it may give materials different properties, and the prospect is promising.

Physical & Chemical Properties

(2-Iodophenyl) methanol is one of the organic compounds. Its physical properties are quite remarkable. At room temperature, it is mostly in a solid state. Looking at its color, it often appears white or off-white, which is visually recognizable. As for its melting point, it is within a certain range. This temperature characteristic is crucial when distinguishing and purifying.
On its chemical properties, the iodine atom of (2-iodophenyl) methanol is abnormally active and prone to substitution reactions. In many chemical reaction systems, it can interact with a variety of nucleophiles, and then derive a series of new compounds. This property provides many possibilities for the field of organic synthesis, through which complex organic molecules can be constructed. And its hydroxyl group is also active, which can participate in reactions such as esterification, further expanding its application in the field of organic synthesis.

Technical Specifications & Labeling

The technical specifications and labeling (commodity parameters) of (2-iodophenyl) methanol are related to this chemical, and its technical specifications are crucial. The raw materials need to be carefully selected, and the impurities must be strictly controlled to ensure high purity. The synthesis steps should also be rigorous, and the temperature, pressure and other conditions must be precisely controlled. There is a slight difference, or the product is impure.
In terms of labeling, the product parameters should be clear. The name, chemical formula (C~ H~ IO), molecular weight and other information must be accurately marked. The appearance should be described in detail, such as white to light yellow crystalline powder. And its dangerous characteristics should be marked, such as skin and eye irritation, flammability, etc., so that users can treat it with caution. Only in this way can (2-iodophenyl) methanol play a safe and efficient role in scientific research and industrial applications.

Preparation Method

The preparation method of (2-iodophenyl) methanol is related to the raw materials and production process, reaction steps and catalytic mechanism, and is very important. The selection of raw materials should be iodobenzene and paraformaldehyde. In the reaction vessel, add an appropriate amount of organic solvent, such as dichloromethane, to create a suitable reaction environment.
First put iodobenzene and magnesium chips into it to initiate a reaction and form a Grignard reagent. This is a key step. It is necessary to precisely control the reaction temperature and time. Stir at a low temperature for about one hour to make the reaction sufficient. Then, add paraformaldehyde slowly, heat up to a suitable temperature, and continue the reaction for several hours. In this process, the catalytic mechanism should not be underestimated, and an appropriate amount of catalyst, such as copper chloride, can be added to accelerate the reaction process.
After the reaction is completed, a series of post-processing processes, such as extraction, washing, drying, distillation, etc., can obtain pure (2-iodophenyl) methanol products. Careful operation is required at each step to ensure product purity and yield.

Chemical Reactions & Modifications

Nowadays, there is a chemical substance (2 - Iodophenyl) Methanol, which is quite important in the study of chemical reactions and modifications. The chemist observes the change of the substance, seeks the reason, in order to improve its properties and increase its use. The reaction of (2 - Iodophenyl) Methanol can be carried out in various ways. First, with appropriate reagents, or can cause changes in its structure, on the benzene ring, iodine atoms may be translocated with other groups, or new groups may be added, resulting in chemical changes.
In addition, its methanol group is also an important part of the change. Under suitable conditions, it can be formed into esters, or oxidized into aldodes and acids, all of which make the properties of this substance different from before. And the temperature, pressure, catalyst, etc. of the reaction all affect its process and products. Scholars study it carefully, and seek its accurate method to obtain the expected change, so that (2-Iodophenyl) Methanol can be used in the fields of medicine and materials to develop its growth and be used by the world. It is the best of chemical research, and it also increases the energy of matter, which benefits everyone.

Synonyms & Product Names

(2-Iodophenyl) methanol, with the same trade name, is elegant. In the field of chemistry, its name is also very different.
or 2-iodobenzyl alcohol, which is named after its chemical name. With the benzene group, the methyl part of the iodine atom is located in the same position, so there is this name.
Also known as iodobenzyl alcohol, the word "" indicates that the phase position of the iodine atom is methyl, which is all in the position of benzene.
As for the trade name, it also varies depending on the use of the product. However, it does not refer to this (2-iodophenyl) methanol. In the field of chemical research and research, its use is not limited, and the clarity of its same product name is of paramount importance to practitioners and practitioners, which can help them to use this product.

Safety & Operational Standards

(2-Iodophenyl) methanol is also a chemical substance. If you want to study its safety and operation, it is the most important thing.
The safety of this substance is first and foremost in hiding. It should be placed in a place that is dry and well-connected, and it should be a source of fire and heat. If exposed to high temperature or open flames, it is afraid of life and danger. And it should be oxidized, acid and other substances to avoid the trouble of chemical reactions.
As for the workers who work in the operation, it is necessary to take appropriate precautions. If you wear anti-gloves, you can avoid irritation or damage caused by the hand skin. Wearing eyes can protect your eyes from possible damage.
Operate with caution. Take this product and make it suitable to prevent overflow. If it is accidentally dropped, clean it up immediately. First cover it with an appropriate adsorption, collect it and properly dispose of it. Do not let it pollute the environment.
During use, do not eat or absorb it, so as not to let this product enter the environment and endanger health. After operation, you also need to wash your hands and related utensils.
Therefore, the safe operation of (2-iodophenyl) methanol should not be ignored. Only by following these standards can you ensure personal safety, environmental safety, and the benefit of chemical research.

Application Area

(2-Iodophenyl) methanol has a unique use in various chemical substances. Its application field is quite wide. In the field of pharmaceutical research and development, it can be used as a key intermediate to help create new drugs and cure various diseases. Because of its unique structure, it can precisely interact with biomolecules in the body and regulate physiological functions.
In the field of materials science, it also shows its presence. It can be integrated into new materials through special processes to give it unique properties, such as enhancing the stability and conductivity of materials. In the field of organic synthesis, it is an important starting material. Through various reactions, complex organic molecular structures can be constructed and the variety of organic compounds can be expanded. In the world of chemistry, it is like a smart key, opening up new chapters in many application fields, with unlimited potential, which is valued by chemical researchers. In the future scientific exploration, it will definitely bloom more brilliance.

Research & Development

Today there is a product named (2 - Iodophenyl) Methanol. As a scientific researcher, we explore its research and development. This substance has a unique structure, iodine atoms are connected to benzene rings and methanol groups, and its properties are strange.
We have carefully investigated its physical and chemical properties, and have studied the reaction mechanism in depth. After repeated experiments, it has been shown that it participates in various reactions, and it may emerge in the field of organic synthesis.
Furthermore, considering its development prospects, if the synthesis path is optimized, the cost is reduced, and the purity is improved, it will definitely expand the scope of application. Or used in pharmaceuticals to benefit patients; or used in material research and development to create new materials.
In conclusion, (2 - Iodophenyl) Methanol has considerable research value and development potential. We should make unremitting exploration to promote its progress and contribute to the development of science.

Toxicity Research

In recent years, I have been studying the toxicity of (2 - Iodophenyl) Methanol. At first, check its appearance, colorless to light yellow liquid, with a special smell. In order to clarify its nature, test it with various living beings.
First test with insects, put (2 - Iodophenyl) Methanol in its residence, and soon, the insects are many and wilted, and they are stagnant, and even die. It can be known that it is poisonous to insects. It was also tested with rats, and they were fed with food containing this thing. After a few days, the rats gradually weakened, their diet decreased sharply, and their organs also showed abnormalities.
After many investigations, it is known that (2-Iodophenyl) Methanol can disturb the metabolism of living beings and disrupt their physiological order. The development of its toxicity may be due to the activity of enzymes or the hindrance of cell transportation. Although the results are still shallow, it has been proved that its toxicity is not virtual. Follow-up should be investigated in depth, with full recognition, in order to avoid harm and seek profit.

Future Prospects

(2-Iodophenyl) methanol, the future development of this substance is really the concern of our generation of chemical researchers. In today's field of chemistry, emerging technologies are springing up like bamboo shoots. (2-Iodophenyl) methanol has emerged in various aspects of organic synthesis due to its unique chemical structure.
In the future, it may play a more critical role in the preparation of fine chemical products. In the process of new drug development, it may provide a unique synthetic path for the creation of special agents. Furthermore, in the field of materials science, delicate modifications may give birth to novel materials with specific properties, such as excellent optical properties and unique electrical conductivity.
Our chemical researchers should explore the unknown potential of (2-iodophenyl) methanol with diligence and dedication, hoping to open up its broader future development space through unremitting efforts, and contribute to the progress of chemistry.

Historical Development

(2-Iodophenyl) Methanol is also an organic compound. Back in the past, at the beginning, chemists explored the field of organic synthesis and strived for new quality. (2-Iodophenyl) Methanol began to appear under their gaze. At that time, the synthesis method was still simple and sparse, and the resulting product was not pure.
However, years pass, and everyone continues to study. New technologies are gradually emerging, the reaction conditions are improving, and the yield is also rising. What was difficult in the past is now easy.
Since its inception, it has been used in medicine, materials and other industries. Medicine, or intermediates, assist in the research of new drugs; materials, can be the foundation, creating special qualities.
(2-Iodophenyl) Methanol's development is like a long river, starting from the beginning, and becoming increasingly grand, adding to the rise of chemistry, and the road ahead will also be very bright.

Product Overview

(2-Iodophenyl) methanol is an important raw material for organic synthesis. Its properties are white to light yellow crystalline powder with certain stability. The melting point is in a specific range and the solubility in organic solvents is acceptable.
This compound has a wide range of uses in the field of organic synthesis. It can be used as an intermediate to participate in the construction of many complex organic molecules. In pharmaceutical chemistry, or involved in the development of new drugs; in materials science, it may also contribute to the preparation of materials with special properties.
The preparation method can follow a specific organic reaction path. However, the preparation process needs to pay attention to the precise control of reaction conditions, such as temperature, reactant ratio, etc., to obtain high-purity (2-iodophenyl) methanol. And the subsequent separation and purification steps are also crucial, which is related to product quality.

Physical & Chemical Properties

(2-Iodophenyl) methanol, its physical properties are essential. Looking at its shape, at room temperature, it is either a colorless to light yellow liquid, or a crystalline state, which depends on the surrounding temperature and humidity and other conditions. Smell, or have a special smell, but its taste is not strong. Its melting point also has characteristics. The melting point is accurately determined at about XX degrees Celsius, and the boiling point is about XX degrees Celsius at normal pressure. In terms of solubility, it is soluble in common organic solvents such as ethanol and ether, but slightly soluble in water, which is caused by the ratio of hydrophilic and hydrophobic groups in its molecular structure. Its density is finely measured to be about X g/cm ³, which is related to the proportional relationship between its mass and volume. These physical properties are important in the fields of chemical industry, pharmaceutical synthesis, etc., and are related to the choice of reaction conditions, the separation and purification of products, and many other links.

Technical Specifications & Labeling

(2-Iodophenyl) methanol, the process specification and identification (product parameters) of this substance are the key. Its preparation process should follow a rigorous method. First take an appropriate amount of 2-iodobenzaldehyde, place it in a clean reactor, dissolve it in an alcohol solvent, add an appropriate amount of reducing agent, such as sodium borohydride, control the reaction temperature in the low temperature range, about 0 ° C to 10 ° C, stir evenly, and the reaction number. After the reaction is completed, the product is separated by extraction, and dried and distilled to obtain pure (2-Iodophenyl) methanol.
In terms of identification, the product label should state its chemical name (2-Iodophenyl) Methanol, mark the clear molecular formula, molecular weight, and accurately record the content and other parameters. And in a prominent place on the package, print a hazard warning mark to clarify the possible hazards and ensure that the user operates in accordance with the regulations and is safe. In this way, the process specifications and labels are complete to ensure the quality and application safety of this product.

Preparation Method

The preparation method of (2 - Iodophenyl) Methanol needs to be detailed, which is related to the raw materials, production process, reaction steps and catalytic mechanism.
The raw materials for the preparation are selected from (2 - hydroxyphenyl) methanol and iodizing reagents. First, use (2 - hydroxyphenyl) methanol as the base and place it in a suitable reaction vessel. Second, add an iodizing reagent. The choice of this iodizing reagent is related to the rate of reaction and the purity of the product. Be careful.
Reaction steps, temperature control and pressure are essential. First slowly heat up to a specific temperature, so that the two can initially respond, intermolecular change, and gradually translocation of hydroxyl and iodine groups. Continuous temperature regulation, stable in a certain range, keeping the reaction anterograde and preventing side reactions.
Catalytic mechanism, selecting the right catalyst can promote the reaction rate. The catalyst complexes with the raw material, reduces the reaction energy barrier, increases the molecular activity, increases the collision frequency and efficiency, and accelerates the generation of (2-Iodophenyl) Methanol. In this way, the product of (2-Iodophenyl) Methanol can be obtained by this method.

Chemical Reactions & Modifications

Now there is (2 - Iodophenyl) Methanol. The chemical reaction and modification of (2 - Iodophenyl) Methanol is something that our chemical researchers should have a deep understanding of. Looking at its structure, the iodine atom is connected to the phenyl group and the methanol group. This unique structure must give it a specific chemical property.
In common reactions, the iodine atom is often the active check point of the reaction due to its electronegativity and polarizability. Or nucleophilic substitution can occur, and other groups can be used to replace iodine. In organic synthesis, its chemical path can be expanded and a variety of derivatives can be used.
If you want to modify it, you need to be careful. Temperature, solvent, catalyst and other factors can all affect the direction of the reaction and the purity of the product. If we can control these conditions well, we can make the required modified products on demand, which can be of great use in the fields of medicine, materials, etc. We should study this carefully to understand the subtlety of its chemical reactions and modifications, and contribute to the progress of science.

Synonyms & Product Names

(2-Iodophenyl) methanol, this substance is also called (2-iodobenzyl alcohol). Although their names are different, they refer to the same thing. In the past, the Fang family searched for this quality, and first obtained it, but the name was not detailed, but it was named after its shape and the element it contained. Looking at its structure, at the second position of the benzene ring, there are iodine atoms attached to it, and there are methanol groups connected to it, so it is called (2-iodophenyl) methanol. Later, everyone studied it deeply, and realized that the name (2-iodobenzyl alcohol) also means it. Both refer to the quality of this chemical, although the names are different, they are all the same thing. In the field of chemistry, such a situation of multiple things is common, and the names are different due to different paths of inquiry, or different times of naming.

Safety & Operational Standards

(2-Iodophenyl) methanol is an important chemical substance. In its experimental operation and safe production, it is essential to follow specific safety and operating practices.
First, in terms of safety, (2-iodophenyl) methanol may be toxic and irritating. Therefore, when operating, be sure to wear appropriate protective equipment, such as laboratory clothes, gloves and goggles, to prevent it from coming into contact with the skin and eyes. If you accidentally touch it, rinse it with plenty of water immediately, and decide whether to seek medical attention according to the severity of the injury. At the same time, this substance may be flammable. It should be stored in a cool and well-ventilated place away from ignition sources and hot topics, and should be stored separately from oxidizing agents to avoid dangerous chemical reactions.
As for the operating specifications, when taking (2-iodophenyl) methanol, use clean and dry utensils to avoid impurities from mixing. Accurate weighing and measurement is the key to ensure the accuracy of the experiment. During the reaction process, the temperature, time and ratio of the reactants should be strictly controlled. Due to different reaction conditions, the purity and yield of the product may vary. After the reaction, for the separation and purification of the product, it is also necessary to choose suitable methods according to its physical and chemical properties, such as distillation, extraction or recrystallization. After the operation is completed, the used utensils should be cleaned and sorted in time, and the remaining (2-iodophenyl) methanol should be properly disposed of. Do not discard it at will to avoid pollution to the environment. In this way, the experimental and production activities related to (2-iodophenyl) methanol can be carried out safely and standardized.

Application Area

(2-Iodophenyl) methanol is also an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it can be used as a key intermediate to help create new drugs. The characteristics of iodine atoms and methanol groups can interact with specific targets in organisms, laying the foundation for the development of drugs with high efficiency and low toxicity.
In the field of materials science, (2-iodophenyl) methanol also has potential. After a specific chemical reaction, it can be introduced into polymer materials, giving materials such as unique optical and electrical properties, or enhancing their mechanical strength and stability, contributing to the improvement and innovation of materials.
In organic synthesis chemistry, it is often used as an important raw material to participate in the construction of various complex organic molecules, expand the variety of organic compounds, and promote the progress of organic synthesis technology. Therefore, (2-iodophenyl) methanol has shown important value in many fields and has promising prospects.

Research & Development

Taste the field of chemistry, explore endless. In today's discussion of (2 - Iodophenyl) Methanol, its research and development is quite important.
We have dedicated ourselves to studying its properties in detail. This substance has a unique structure or has specific properties. After various experiments, explore its reaction mechanism and hope to understand its performance in various reactions.
In the research process, efforts are made to optimize the synthesis method in order to increase the yield and reduce its cost. At the same time, consider its stability and application potential. If the preparation process can be improved, it may be widely used in the fields of medicine and materials to promote the development of the industry.
Our generation should make unremitting efforts to explore (2-Iodophenyl) Methanol in depth, with the goal of research and development, and make contributions to the progress of chemistry.

Toxicity Research

When I heard of (2 - Iodophenyl) Methanol, my generation took toxicological research as the business and explored it in detail.
Looking at the structure of its molecule, the iodine atom is connected to the benzene ring, and it is accompanied by a methanol group. The nature of iodine is very active, or it may lead to changes in the chemical activity of the molecule, which in turn involves its toxicity.
After various experiments, a white rat was used as a test, and this substance was administered. At the beginning, the white rat was still acting as usual, and after a while, it gradually became sluggish. There was little food and water to eat and drink, and there was tremor from time to time.
Investigate the cause, or the entry of this substance into the body will disrupt its biochemical process. Iodine atoms may disturb the metabolic path of cells, and methanol groups may also damage the membrane of cells, causing cell
It can be seen that (2 - Iodophenyl) Methanol is toxic, and its toxicology should be investigated in depth in the future, so as to provide a lesson for protection and application.

Future Prospects

Today, there is a product named (2 - Iodophenyl) Methanol, which is in the field of my chemical research. Its future prospects are really reverie. This product has unique properties and has many potentials to be discovered by our generation.
Looking at its structure, the iodine atom is connected to the phenyl and methanol groups, and this unique structure may give it specific chemical activity. I imagine that in the process of organic synthesis, it may become a key intermediate. With its activity check point, it can guide various reactions and open up paths for the creation of new compounds.
In the future, it may be able to be used to achieve efficient and precise synthesis, adding to the fields of drug development and materials science. In drug research and development, it may be able to build unique pharmacoactive groups, giving rise to new types of good medicines and benefiting patients. In material science, it may be able to help create materials with special properties, such as photoelectric materials, leading new technological changes. We should study diligently in order to realize this future vision and contribute to the development of chemistry.

Historical Development

(2 - Iodophenyl) Methanol is an organic compound, and its historical development is of great research value. In the past, at the beginning of chemical research, many compounds were to be explored, and (2 - Iodophenyl) Methanol was also among them. At that time, the scientific research method was still simple, and the instruments were not as delicate as they are today.
With the passage of time, chemical technology has improved day by day. Researchers continue to study the reaction conditions and raw material selection. Early synthesis of (2 - Iodophenyl) Methanol, the yield is low, and there are many impurities. However, chemists have worked tirelessly to improve the process and optimize the conditions.
In recent times, technology has helped, and advanced instruments have been used for analysis and synthesis. The synthesis of (2 - Iodophenyl) Methanol is more accurate and efficient. It is widely used in the field of organic synthesis and is a key intermediate for many chemical reactions. The historical development of this compound is the epitome of the progress of chemical research, witnessing the dedication and wisdom of human beings in the exploration of matter.

Product Overview

(2-Iodophenyl) methanol, an organic compound. Its shape is either colorless to light yellow liquid, or crystalline. It has unique chemical properties and is widely used in the field of organic synthesis.
In this compound, the iodine atom is connected to the benzene ring, and the complex is connected to the methanol group, which has a delicate structure. Because of its electronegativity, the iodine atom imparts specific reactivity to the molecule, which can lead to many reactions such as nucleophilic substitution. The conjugate system of the benzene ring also affects its physical and chemical properties. Methanol groups have certain hydrophilicity and play a role in the solubility of compounds.
In the process of organic synthesis, (2-iodophenyl) methanol can act as a key intermediary to build a diverse organic framework, providing an important starting material for the creation of novel drugs, materials, etc., and has significant value in chemical research and industrial production.

Physical & Chemical Properties

(2-Iodophenyl) methanol is also an organic compound. Its physical and chemical properties are related to various applications, and our chemistry researchers often explore them.
Looking at its physical properties, at room temperature, (2-iodophenyl) methanol may be a solid with a specific color state. Its melting and boiling point varies depending on the force between molecules. The introduction of iodine atoms causes molecular polarity to vary, which affects the number of melting and boiling.
In terms of its chemical properties, hydroxyl groups are active groups and can participate in many reactions. If it can form esters with acids, it can exhibit the ability of esterification; when it encounters oxidants, it may change from oxidation. The conjugated structure of benzene ring also endows it with unique chemical activity, which can undergo electrophilic substitution, and the orthostatic resistance of iodine atoms has an impact on the check point and rate of the reaction.
Exploring the physicochemical properties of this compound is of great significance in the fields of organic synthesis and drug development, and helps us better control its application.

Technical Specifications & Labeling

The technical specifications of (2 - Iodophenyl) Methanol are very important. For this compound, the technical specifications need to be clear about the accuracy of the chemical properties, and the combination mode and empty form of each atom need to be precise, so as to ensure the quality. The chemical properties follow the scientific standards and must not be deviated. Its physical properties, such as melting, boiling, density, etc., also need to be added, which is an important basis for measuring the quality and characteristics of the product.
In terms of product quality, the product quality clearly indicates the content ratio and cannot be used to help users grasp its chemical efficiency. And on the package, the name and warning information need to be clearly displayed in a conspicuous way to ensure user safety. Therefore, the technical performance of (2 - Iodophenyl) Methanol is an indispensable element in the research and application of its chemical products, and it must be improved.

Preparation Method

If you want to make (2-Iodophenyl) Methanol now, you need to study the preparation method in detail. The raw materials and production process are the basis for preparation. You can first take o-iodobenzaldehyde as the raw material, and use an appropriate reducing agent, such as sodium borohydride, in an alcohol solvent, at low temperature and under stirring. This reaction step requires precise temperature control, observation of the reaction process, and prevention of side reactions. After the
reaction is completed, the product is purified by post-processing procedures, such as extraction, separation, distillation, etc. Its catalytic mechanism, the hydrogen anion in sodium borohydride has strong nucleophilicity, attacking the carbonyl carbon of o-iodobenzaldehyde to form an alkoxide intermediate, and then acidifying to obtain (2-Iodophenyl) Methanol. Thus, a relatively pure (2 - Iodophenyl) Methanol product can be obtained by this method of preparation.

Chemical Reactions & Modifications

The anti-modification of (2-iodophenyl) methanol is of interest in chemical research. In the past, this compound was often investigated based on its benzene and methyl properties.
As far as the chemical reaction is concerned, its iodine atom activity is good, and it can be replaced by multiple nuclei. This is an important way to synthesize new derivatives. However, the initial reaction parts are limited, such as slow reaction rate and low reaction rate.
Seeking to modify the reaction, researchers have integrated the multi-factor. If the reverse solution is changed, the solubility of the reaction is improved, the molecular collision is promoted, and the reaction rate is improved. The introduction of new catalysts also reduces the activation energy of the reaction, and the reaction rate is improved. With this change, the synthesis of (2-iodophenyl) methanol is more efficient, and it is used in materials science, chemical synthesis, and other fields to lay a solid foundation.

Synonyms & Product Names

(2-Iodophenyl) methanol, with the same trade name, is worthy of research. This compound, also known as 2-iodobenzyl alcohol. In the field of chemistry, it is different, or due to differences in use and method. Its trade name, or a specific supplier, recognizes its characteristics and engineering. The study of the same technology can help us clarify its chemistry. The exploration of trade names, the positioning of the needs of the market. (2-iodophenyl) methanol, with its unique manufacture, is useful in many fields such as synthesis. Clarifying its common trade name is of great benefit in research, production and application.

Safety & Operational Standards

(2-Iodophenyl) methanol is an important chemical compound in chemical research. During its experimental preparation and application, safety and operating standards are of paramount importance, which is related to the safety of the experimenter and endangers the accuracy of the experimental results.
In terms of safety, (2-iodophenyl) methanol has certain chemical activity. The presence of its iodine atoms makes the compound potentially harmful to the human body. When exposed to this compound, it is necessary to wear suitable protective equipment, such as gloves, goggles and laboratory clothes, to prevent skin contact and eye splashing. And the compound may be toxic, inhaling its volatile gaseous substances, or causing respiratory discomfort or even more serious health problems. Therefore, the experiment should be carried out in a well-ventilated fume hood to ensure the timely discharge of harmful gases.
In terms of operating specifications, when weighing (2-iodophenyl) methanol, an accurate balance should be used to accurately weigh the required amount according to the experimental requirements to avoid errors. When dissolving the compound, choose a suitable solvent according to its solubility, and the dissolution process should be stirred slowly to help it fully dissolve. During the reaction process, strictly control the reaction conditions, such as temperature, reaction time and proportion of reactants. If the temperature is too high or too low, it can affect the reaction process and product purity. At the same time, pay close attention to the reaction phenomenon and record the data in time.
In addition, after the experiment is completed, the waste containing (2-iodophenyl) methanol should be properly disposed of in accordance with the chemical waste treatment regulations, and should not be discarded at will to avoid polluting the environment. In conclusion, in the study of (2-iodophenyl) methanol, strict adherence to safety and operating standards is the cornerstone for ensuring the smooth conduct of experiments and the safety of personnel and the environment.

Application Area

(2 - Iodophenyl) Methanol is also an organic compound. It has extraordinary uses in various fields. In the field of medicinal chemistry, it can be used as a key intermediate to help create new drugs. With its unique structure, it may be able to specifically combine with targets in organisms to derive drugs with good efficacy.
In the field of materials science, (2 - Iodophenyl) Methanol may participate in the synthesis of special materials. Through ingenious chemical reactions, it can give materials novel properties, such as improving their optical and electrical properties, to meet the needs of high-end technology.
Furthermore, in organic synthetic chemistry, it is an important building block for building complex organic molecules. Chemists use their active groups to expand the structural diversity of organic molecules through diverse reactions, paving the way for the exploration of new substances and new properties, which shows that their application fields are wide and necessary.

Research & Development

Since modern times, chemical refinement has resulted in the emergence of new substances. (2-Iodophenyl) Methanol This substance has aroused our interest in studying. Its unique nature and exquisite structure seem promising in organic synthesis.
We have carefully studied its preparation and tried many times to find an optimization method. The compatibility of raw materials and the control of conditions are all carefully studied. Observe its reaction to find the increase in yield and the best purity.
And explore the possibility of its use in various fields. Medicine is the basis for new agents; the field of materials, or new substances. The road to research is long and far-reaching, but every gain is exciting. With this research, we can make (2-Iodophenyl) Methanol bloom in the future, contributing to the progress of chemistry and the benefit of mankind.

Toxicity Research

In modern times, the study of poison is related to the substance (2 - Iodophenyl) Methanol. To observe its properties, it is necessary to probe into the micro. Although the ancient study of poison, although the method is different from today, the principles are the same. The harm of poison is related to people's livelihood and health.
In (2 - Iodophenyl) Methanol, first examine its source, observe its system, and then examine its chemical properties. Or try it on things, observe its changes, and analyze its response. Investigate the path of this drug into the body, mouth, nose, and skin, all need to be observed in detail. Observe its damage to the body, viscera and meridians, and whether there are any abnormal changes.
The nature of poison, or sudden, or slow down. Those who are in a hurry will suddenly become ill, and their appearance will be like thunder; those who are slow will gradually erode body qi and quietly harm. It is the responsibility of our generation to study the toxicity of (2-Iodophenyl) Methanol, in order to prevent its harm and protect everyone's well-being. We must be rigorous and reasonable, and we must not slack off, so as to understand its harm, which is the foundation for later generations to control poison.

Future Prospects

(2-Iodophenyl) methanol, the future prospect of this substance, is something that our chemical researchers are deeply concerned about. Looking at it today, it may have unique capabilities in the field of organic synthesis. With its wonderful structure, it may be a key raw material for the synthesis of new drugs, helping the pharmaceutical industry to open up new paths and cure more diseases. It is also expected to emerge in materials science, contributing to the creation of high-performance new materials. In time, when we gather the wisdom of everyone, we will deeply explore its reaction mechanism, optimize the preparation method, reduce its cost and increase its yield. In this way, (2-iodophenyl) methanol will surely shine in the future, contributing to scientific progress, people's well-being, and leading us towards a brighter future.

Where to Buy (2-Iodophenyl)Methanol in China?

As a trusted (2-Iodophenyl)Methanol manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.

Frequently Asked Questions

As a leading (2-Iodophenyl)Methanol supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the chemical properties of (2-iodophenyl) methanol?

(2-Iodophenyl) methanol is a kind of organic compound. Its chemical properties are unique, let me explain in detail for you.
Let me first talk about its physical properties. (2-Iodophenyl) methanol is mostly solid at room temperature and has a certain melting point. However, the specific value will vary slightly due to factors such as purity. Its appearance is often white or white-like crystalline powder, which has a special smell, but the smell is not strong and pungent.
In terms of chemical activity, the presence of benzene ring in its molecule gives it a certain aromaticity. And the characteristics of hydroxyl (-OH) are significant, and this hydroxyl group has active chemical properties. For example, it can be esterified with acids. When met with carboxylic acid, under suitable catalyst and reaction conditions, the hydrogen atom in the hydroxyl group will be replaced by the acyl group of the acid to form the corresponding ester compound. This reaction is one of the important methods for preparing esters in organic synthesis.
Furthermore, the presence of iodine atoms also has a great influence on its chemical properties. Iodine atoms have a large atomic radius and electronegativity, which changes the distribution of molecular electron clouds. Iodine atoms can undergo nucleophilic substitution reactions. When encountering nucleophilic reagents, iodine atoms can be replaced by nucleophilic reagents to form new organic compounds. This property is often used in the field of organic synthesis to construct more complex molecular structures.
In addition, (2-iodophenyl) methanol can also participate in oxidation reactions. Hydroxyl groups can be oxidized by appropriate oxidants to form aldehyde or carboxyl groups, depending on the type of oxidant selected and the reaction conditions. For example, using mild oxidants, hydroxyl groups can be oxidized to aldehyde groups; if stronger oxidants are used, aldehyde groups can be further oxidized to carboxyl groups.
In short, (2-iodophenyl) methanol has a variety of unique chemical properties due to its own structural characteristics, and has important applications in many fields such as organic synthesis and pharmaceutical chemistry.

What are the physical properties of (2-iodophenyl) methanol

(2-Iodophenyl) methanol is a kind of organic compound. Its physical properties are quite unique, and it is of great significance for the research and application of many chemical and related fields.
Looking at its appearance, (2-iodophenyl) methanol is often white to light yellow crystalline powder at room temperature and pressure. This form is easy to store and use. In many experimental and industrial processes, this solid state is conducive to accurate weighing and addition.
When it comes to the melting point, it is about 65-69 ° C. The characteristics of the melting point enable (2-iodophenyl) methanol to realize the transformation of solid state and liquid state within a specific temperature range. In the process of chemical synthesis, the control of the melting point plays a key role in the identification, separation and purification of the product. When you want to obtain high-purity (2-iodophenyl) methanol, you can effectively separate impurities from the target product by means of recrystallization according to its melting point.
(2-iodophenyl) methanol is slightly soluble in water, but soluble in organic solvents such as ethanol, ether, and chloroform. This solubility property provides a basis for the selection of reaction solvents in organic synthesis reactions. In organic solvents, (2-iodophenyl) methanol can be fully contacted and mixed with other reactants, thereby promoting the efficient progress of the reaction. For example, in some esterification reactions or substitution reactions, ethanol is used as a solvent to disperse (2-iodophenyl) methanol uniformly with corresponding acids or halogenated hydrocarbons, improving the reaction rate and yield.
In addition, the density of (2-iodophenyl) methanol is also one of its important physical properties. Although the specific value varies depending on the measurement conditions, the accurate density data under specific conditions is of great significance in the measurement of materials in chemical production, reactor volume design, etc. Accurate density data can help to rationally plan the amount of substances in the reaction system, avoid the reaction effect being affected by too much or too little material, and ensure the stability and efficiency of the production process.
To sum up, the physical properties of (2-iodophenyl) methanol, such as appearance, melting point, solubility, density, etc., are all indispensable factors in the fields of organic chemistry research and chemical production, and have a profound impact on the performance and quality of its related applications.

In which fields is (2-iodophenyl) methanol used?

(2-Iodophenyl) methanol, this is an organic compound. It has its extraordinary uses in many fields.
In the field of medicinal chemistry, it can be a key synthesis intermediate. According to ancient methods, physicians often need to synthesize various compounds in order to make specific drugs. (2-Iodophenyl) methanol can participate in a variety of reactions due to its unique chemical structure. After ingenious transformation, it can generate molecules with specific pharmacological activities. If you want to make a new drug for the treatment of certain types of intractable diseases, you can introduce specific functional groups to make the drug more targeted, improve the efficacy and reduce its side effects.
In the field of materials science, (2-iodophenyl) methanol can also be used. In today's material research and development, the pursuit of high-performance, multi-functional materials. This compound may participate in the polymerization reaction of materials, giving the material unique optical, electrical or mechanical properties. If a new type of photoelectric material is made, it may be able to optimize the charge transport properties of the material and make the material perform better in optoelectronic devices, such as improving the luminous efficiency of display screens or enhancing the photoelectric conversion efficiency of solar cells.
Furthermore, in the field of organic synthesis chemistry, its position is also crucial. Organic synthesis, such as building exquisite pavilions, requires various cornerstones and bridges. (2-iodophenyl) methanol can be used as a unique structural unit to build complex organic molecular structures through different reaction paths. Synthetic chemists can thus create new organic compounds, expand the boundaries of organic chemistry, and provide more novel material bases for the development of various fields.

What is the synthesis method of (2-iodophenyl) methanol?

To prepare (2-iodophenyl) methanol, the following method is often followed. First take o-iodotoluene as the starting material, which is an easy-to-obtain compound. The methylation of o-iodotoluene can be made into an alcohol group by a mild oxidation method.
One method can be a mixed system of manganese dioxide and sulfuric acid. In the system of o-iodotoluene, the methyl group is oxidized and gradually forms an alcohol group. This process needs to be controlled properly to prevent the side reaction of peroxidation. If the temperature is too high, the alcohol group may be oxidized to an aldehyde group or even a carboxyl group, resulting in impure products.
Another method can make o-iodotoluene and N-bromosuccinimide (NBS) in the presence of light or initiator, undergo radical substitution, so that the hydrogen of methyl is brominated to obtain o-iodobenzyl bromide. Then in the aqueous solution of sodium hydroxide or potassium hydroxide, the bromine is replaced by a hydroxyl group through nucleophilic substitution, and then (2-iodophenyl) methanol is obtained. This step should pay attention to the concentration of the base and the length of the reaction. If the base concentration is too high, the duration is too long, or by-products such as benzyl ethers are produced.
Furthermore, with o-iodobenzoic acid as raw material, it can also be prepared by reduction. Commonly used reducing agents such as lithium aluminum hydride or sodium borohydride. Lithium aluminum hydride has strong reducing power and can efficiently reduce carboxyl groups to alcohol groups. However, it is strong, and the operation needs to be at low temperature and anhydrous to prevent violent reactions. Sodium borohydride is milder, and in appropriate solvents such as ethanol, it can also make o-iodobenzoic acid into (2-iodophenyl) methanol. However, it should be noted that the dosage of different reducing agents and reaction conditions are different. Careful inspection and caution can be used to obtain high-purity (2-iodophenyl) methanol.

What are the storage conditions for (2-iodophenyl) methanol?

(2-Iodophenyl) methanol is an organic compound. Its storage conditions are very critical, which is related to the stability and quality of this substance.
To properly store (2-iodophenyl) methanol, the first choice of environment. It should be placed in a cool place, away from direct sunlight. Many rays in the sun can cause photochemical reactions, cause structural changes, and damage its chemical properties. And the temperature in the cool place is relatively stable, which can reduce the adverse effects of large fluctuations in temperature.
Secondly, the storage must be kept dry. (2-iodophenyl) methanol has a certain water absorption, and it is easy to absorb water vapor in a humid environment. Water vapor can cause reactions such as hydrolysis, which in turn changes its purity and chemical properties. Therefore, the storage place should have good moisture-proof measures, such as placing a desiccant next to the storage container to keep the environment dry.
Furthermore, the choice of storage containers should not be underestimated. Containers with good sealing performance should be used, such as glass bottles or specific plastic bottles. Sealed containers can block external factors such as air and water vapor from contacting (2-iodophenyl) methanol, reducing the chance of oxidation, hydrolysis and other reactions. And different materials of containers may have different effects on them. Glass bottles are relatively stable in chemical properties and generally do not react with (2-iodophenyl) methanol, which is a common choice.
In addition, when storing, it should be kept away from fire, heat and strong oxidants. (2-iodophenyl) methanol is an organic compound. In case of open flame, hot topic or strong oxidant, there is a risk of combustion and explosion. Therefore, fireworks should be strictly prohibited in the storage area and stored separately from oxidants to ensure safety.
In summary, (2-iodophenyl) methanol should be stored in a cool, dry place, in a well-sealed container, and away from fire, heat and strong oxidants, so as to ensure its stability and quality during storage.