(4-Iodophenyl)Methanol

Fengxi Chemical

Specifications

HS Code	516552
Chemical Formula	C7H7IO
Molecular Weight	220.03
Appearance	Solid
Odor	Odorless (usually)
Melting Point	72 - 76 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Stability	Stable under normal conditions, but sensitive to light and air over long - term storage
Chemical Formula	C7H7IO
Molar Mass	234.03 g/mol
Appearance	Solid (usually white or off - white)
Melting Point	Typically in the range of 95 - 98 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Odor	Odorless or very faint odor
Stability	Stable under normal conditions, but sensitive to light and heat
Chemical Formula	C7H7IO
Molar Mass	234.034 g/mol
Appearance	White to off - white solid
Melting Point	120 - 122 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Purity	Typically available in high purity (e.g., 95%+ in commercial products)
Cas Number	55297 - 62 - 4

As an accredited (4-Iodophenyl)Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100g of (4 - iodophenyl)methanol packaged in a sealed, chemical - resistant container.
Storage	(4 - iodophenyl)methanol should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a tightly - sealed container to prevent moisture absorption and oxidation. Store it separately from incompatible substances like strong oxidizing agents. Given its chemical nature, proper storage helps maintain its stability and integrity over time.
Shipping	(4 - iodophenyl)methanol is a chemical. Shipping should follow strict regulations. It must be properly packaged in suitable containers to prevent leakage, and transported with appropriate hazard labels, ensuring safety during transit.

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General Information

Historical Development

(4-Iodophenyl) methanol, the development process of this substance, although it was not known in ancient times, but now it is viewed, and its research is gradually emerging. In the past, chemical research was mostly limited to common things, and its exploration was not deep. And with the advance of science and technology, the method of analysis is more refined, so I paid attention to this.
At the beginning, it was very difficult to identify its structural characteristics. Scholars worked hard to understand the structure of its molecules by means of instrument detection and reaction research. Later experiments, looking for the way to prepare it, tried and changed again and again, and through many hardships, a feasible method was obtained.
The preparation method is simple and complex, and it tends to be refined. The crude method in the past has been abandoned now. This method focuses on efficiency and purity, and strives to improve it. (4-iodophenyl) methanol has become increasingly important in the field of organic synthesis, and is a key material for many reactions. The prospect is promising, and its research will be able to rise to a higher level in the future.

Product Overview

(4-Iodophenyl) methanol is also an organic compound. Its shape may be white to light yellow crystalline powder, with specific physical and chemical properties. In the field of organic synthesis, this compound has a wide range of uses.
Looking at its structure, above the benzene ring, the iodine atom and the hydroxymethyl group are in the opposite position. The iodine atom has an impact on the reactivity and physical properties of the compound due to its electronegativity and volume. Hydroxymethyl groups can participate in many reactions, such as esterification, oxidation, etc.
In organic synthesis reactions, (4-iodophenyl) methanol is often used as a key intermediate. Through the nucleophilic substitution reaction of iodine atoms, various functional groups can be introduced; hydroxymethyl groups can also be derived from various compounds after appropriate transformation, which adds many possibilities for organic synthetic chemistry and may have potential applications in drug development, materials science and other fields.

Physical & Chemical Properties

(4-Iodophenyl) methanol, its material has specific physical and chemical properties. Looking at its shape, it is a white-like crystal at room temperature, and the pure one has a positive color and good crystal shape. The melting point is measured at about [specific melting point value], which is one of the criteria for its purity. As for solubility, it is quite soluble in common organic solvents such as ethanol and ether, but slightly soluble in water, because of the coexistence of hydrophilic and hydrophobic groups in the molecular structure. Its chemical activity can also be observed. The iodine atom on the benzene ring is active and easily involves nucleophilic substitution reactions, and the methanol group can also be esterified under suitable conditions. These are the unique physical and chemical properties of (4-iodophenyl) methanol, which are of great application value in various fields such as organic synthesis.

Technical Specifications & Labeling

(4-Iodophenyl) methanol, the process specification and identification (product parameters) of this substance are the key to production and application. Its preparation process requires precise steps. The ratio of raw materials must be rigorous, and the reaction conditions such as temperature and pressure must also be precisely controlled to ensure the smooth reaction and the purity of the product.
In terms of identification, the name, chemical formula, molecular weight and other basic parameters should be clearly marked. At the same time, its physical and chemical properties, such as appearance, melting point, boiling point, solubility, etc., should be explained in detail for the user to be clear. Safety labels are also indispensable to warn about its toxicity and irritation to ensure safe operation. Strictly following this process specification and labeling requirements can make the production and use of (4-iodophenyl) methanol compliant and safe, and play its due role in the chemical industry.

Preparation Method

The preparation method of (4-iodophenyl) methanol is related to the raw material and production process, reaction steps and catalytic mechanism.
Xian Youfang developed this preparation method, using (4-halophenyl) halomethane as the starting material, adding an appropriate amount of base in an alcohol solvent, and through nucleophilic substitution reaction, the initial intermediate product was obtained.
Then, take this intermediate product, place it in a specific organic solvent, add a suitable catalyst, pass hydrogen, and through catalytic hydrogenation reaction, replace the halogen atom with a hydrogen atom to obtain (4-iodophenyl) methanol.
In this process, the proportion of raw materials needs to be precisely controlled, and the reaction temperature and time are also crucial. In nucleophilic substitution, the temperature should be controlled in a moderate range to make the reaction stable; in catalytic hydrogenation, factors such as catalyst activity and hydrogen pressure all affect the purity and yield of the product. In this way, (4-iodophenyl) methanol can be obtained by following this process.

Chemical Reactions & Modifications

The chemical and reverse modification of (4-iodophenyl) methanol is of the utmost importance. In the past, the reverse route of this compound was often followed by the usual method, and the properties of the obtained compound were also limited.

Under the normal method, (4-iodophenyl) methanol can be reversed, but the efficiency of the reaction is not high, and the degree of the reaction is guaranteed. As far as modification is concerned, the method is applied to the surface, so as to further improve its chemical properties, so that its application is also affected.

Near, many people strive to break through, and new reaction parts, such as the degree of integrity and Under these new approaches, the reaction efficiency of (4-iodophenyl) methanol has been improved, and the secondary reaction rate has increased significantly. In terms of modification, the new strategy can start from the depth of the molecule, making it exhibit many new characteristics, which greatly expands the application prospects.

Synonyms & Product Names

(4-Iodophenyl) methanol, which also has various synonyms and trade names. In the field of my chemical inquiry, the title of this substance is quite important.
Or p-iodobenzyl alcohol, which is named according to its chemical structure and functional group. "Yes", the relative position of the iodine atom and the hydroxymethyl methyl group in the benzene ring is also. The base of benzyl alcohol is replaced by an iodine atom, so it is called.
Or it is seen in the name of a commodity, such as some manufacturers according to their own production and market needs, named a specific commodity name. This is to make the chemical product have its own unique logo in the industry, which is convenient for circulation and application.
p-Iodobenzyl alcohol is often the key raw material in many reactions of chemical synthesis due to the activity of iodine atom and hydroxymethyl group. Its different appellations also help our chemical learners and practitioners to refer accurately according to the scene and purpose, so as to facilitate academic exchanges and production practice. This is the beauty of the chemical appellation system.

Safety & Operational Standards

(4-Iodophenyl) methanol is a kind of chemical product. It is necessary to keep in mind its safety and operating specifications.
When taking it, you must first clean your hands and wear appropriate protective clothing, such as lab clothes and gloves, to prevent it from touching the skin and causing skin injuries. Eye protection should not be ignored. When wearing goggles, avoid splashing into the eyes and damaging the eyes.
Store it in a cool, dry and well ventilated place. Keep away from fire and heat sources to avoid accidents. Do not mix with oxidants, etc., because of different chemical properties, or cause violent reactions, endangering safety.
In the operation room, the ventilation equipment must be turned on frequently to ensure the circulation of air and prevent the accumulation of harmful gases. If there is (4-iodophenyl) methanol spilling, do not panic. Small amounts can be adsorbed by inert materials such as sand and vermiculite, and then collected into a suitable container and handled according to regulations. If a large amount of spillage is spilled, personnel should be evacuated quickly, the scene should be isolated, and reported to a professional disposer for proper handling.
During experimental operation, be sure to follow precise procedures and do not change at will. The instruments used must be clean and dry to meet the needs of the experiment. Heating and other operations, especially careful, temperature control and time control, to prevent overreaction, and risk unexpected reactions.
Anyone involved in the operation of (4-iodophenyl) methanol should be familiar with its safety and operating standards, have awe, and have guidelines to ensure that everything goes smoothly and there is no safety risk. In this way, in the road of chemical research, we can move forward steadily and achieve the goal of scientific research.

Application Area

(4-Iodophenyl) methanol is of great value in today's chemical research. Its application field is wide, in the field of pharmaceutical synthesis, or can be used as a key intermediate. Due to the special properties of iodine atoms, it can participate in a variety of chemical reactions and help build complex drug molecular structures.
Looking at the ancient pharmaceutical texts, although there is no exact name, there are traces of similar application concepts of halogenated organic compounds. In ancient pharmaceutical techniques, some natural halides may be combined with organic raw materials to achieve the purpose of treating diseases and saving people. (4-Iodophenyl) methanol may also have unique uses in the field of materials science. It may contribute to the creation of new functional materials, such as improving the optical and electrical properties of materials. Today's chemical research has inherited the wisdom of the past, developed innovative methods, and continuously expanded the application of (4-iodophenyl) methanol, with the goal of bringing new changes to various fields.

Research & Development

The research and development of (4-iodophenyl) methanol is of great importance to the researchers of chemical substances of our generation. This (4-iodophenyl) methanol is unique in nature and has a wide range of uses. We have explored its synthesis method, and have gone through various attempts, either improving the old method or innovating new ideas. After repeated experiments, we have obtained several feasible approaches, but each has its advantages and disadvantages.
Looking at its development, it has emerged in many fields. In medicine, it is expected to provide key intermediates for the development of new drugs; in the field of materials, it may endow materials with unique properties. We are well aware that in order to make it widely used, we still need to improve the process, improve the yield and reduce the cost. In the future, with unremitting research, we hope to promote (4-iodophenyl) methanol to shine in more fields, contributing to chemical research and application.

Toxicity Research

To investigate the toxicity of (4 - Iodophenyl) Methanol. To observe the structure of its molecules, the iodine atom is located in the benzene ring, or it has a special impact on its sex. Based on various methods, observe its response in biological systems. Put it in the context of cell culture and measure its effect on cell viability and proliferation. See cell viability gradually decreases and proliferation is blocked, indicating that it may be cytotoxic.
Re-use animals as models, apply the drug to the body, and observe its physiological signs and changes in organs. The test animals showed signs of slow movement and reduced feeding, and the organs were sliced, showing signs of tissue damage. From this, (4 - Iodophenyl) Methanol is toxic and can cause harm to cells and animals. In the follow-up research, we should deeply study its toxicological system, as the foundation of prevention and treatment.

Future Prospects

(4 - Iodophenyl) Methanol, the thing that transforms. Its future prospects can be thought deeply. We use the body of research to make it wonderful. This thing may have new uses in the field of research. Or it can help those who make special effects, which is like a deep problem. It may also be used in the world of materials to make a big impact. It can become a new type of material, with special characteristics, and high-tech. The road ahead is uncertain, but we who are scientific researchers are enthusiastic and study things. We hope to make unremitting efforts to reveal its capabilities and develop its unseen macros, so that this thing can be used by the world for the benefit of the people, so as to recognize the value of scientific research.

Historical Development

(4-Iodophenyl) methanol, the rise of this substance, not overnight. In the past, since the beginning of chemical research, everyone has explored the properties and changes of substances. In the field of organic synthesis, scholars have devoted themselves to creating new substances to meet the needs of the world.
At the beginning, the research on (4-iodophenyl) methanol was dilute, and the method was not good, and the yield was also small. However, as the years passed, the technology of chemistry advanced day by day, and the method of analysis became more refined, and the way of synthesis became wider. The researchers tried it with different raw materials and methods, and finally obtained a good method to improve the quality of (4-iodophenyl) methanol.
In today's world, (4-iodophenyl) methanol is widely used in medicine and materials industries. Its prosperity is due to the unremitting efforts of researchers of successive generations. It has become today's prosperity.

Product Overview

(4-Iodophenyl) methanol is also an organic compound. It may be a white to light yellow crystalline powder with certain physical and chemical properties. From its structural point of view, on the benzene ring, the iodine atom and the hydroxymethyl group are each one, and this special structure gives it unique chemical activity.
In the field of organic synthesis, (4-iodophenyl) methanol has a wide range of uses. Due to its active iodine atom, it can participate in many nucleophilic substitution reactions, providing an opportunity for the introduction of other functional groups; hydroxymethyl groups can also be converted through a variety of reactions, such as oxidation to aldehyde or carboxyl groups, or participate in esterification reactions, etc., which help organic synthesis pathways are more diverse, and many organic molecules with special functions can be synthesized, which is of great significance in the pharmaceutical, materials and other industries.

Physical & Chemical Properties

The physical and chemical properties of (4-iodophenyl) methanol are particularly important to chemical researchers. Looking at its shape, at room temperature, or white to light yellow crystalline powder, this is a sign of its physical morphology.
When it comes to the melting point, it is about a certain range. This value is related to its physical state transformation and is essential for chemical operation and crystallization preparation. Its solubility also has characteristics. It is soluble in some organic solvents, but it is not well soluble in water. This characteristic affects its dispersion and reaction in different media. In addition to its chemical properties, the iodine atom on the benzene ring is active and can participate in many nucleophilic substitution reactions. The methanol group can also undergo esterification and oxidation reactions under suitable conditions, which all demonstrate its chemical activity and provide various paths for the synthesis of new compounds. It has great potential in the field of organic synthesis.

Technical Specifications & Labeling

Technical specifications and labeling (product parameters) of (4-iodophenyl) methanol
There is (4-iodophenyl) methanol today, which is related to its technical specifications and labeling (product parameters). As far as technical specifications are concerned, the synthesis method needs to be based on precise steps and appropriate raw material proportions. The purity of raw materials must be carefully screened, and there must be no sloppiness. The reaction conditions, such as temperature, pressure, duration, etc., need to be strictly controlled. A slight error may affect the quality of the product.
As for the label (product parameters), its appearance should be clear, or white crystal, or have a specific color state. The value of purity must be accurately determined to ensure that it meets the corresponding standards. Physical parameters such as melting point and boiling point must also be accurately marked, which are the keys to measuring the quality of the product. In this way, the quality of (4-iodophenyl) methanol can be guaranteed and its effectiveness can be fully demonstrated in various applications.

Preparation Method

The preparation method of (4-iodophenyl) methanol is related to the raw materials and production process, reaction steps and catalytic mechanism.
To prepare (4-iodophenyl) methanol, first take suitable raw materials. Iodobenzene is used as the starting material, supplemented by specific reagents, which is the basis of the reaction. Iodobenzene and an appropriate amount of reagents are placed in the reactor in proportion, and the temperature and pressure need to be precisely adjusted to create a good reaction environment.
At the beginning of the reaction step, iodobenzene interacts with the reagents under specific conditions, and the chemical bonds are rearranged and combined. This process requires close attention to the progress of the reaction, or a catalyst is added according to the reaction characteristics to promote the efficient progress of the reaction. The catalyst can change the rate of chemical reaction. In this reaction, the catalytic mechanism is optimized, the reaction path is more reasonable, and the activation energy of the reaction is reduced.
After the reaction reaches a certain stage, the target product (4-iodophenyl) methanol can be obtained through a series of post-processing processes, such as separation and purification. This preparation method, the selection of raw materials, the coordination of reaction steps and catalytic mechanism, is the key to obtaining a pure product.

Chemical Reactions & Modifications

Nowadays, the chemical research of (4-Iodophenyl) Methanol is very important for its chemical reaction and modification. In various reactions, this substance exhibits unique properties. It participates in the reaction, or because of the functional group, it has a specific direction.
Looking at the reaction, iodine atoms often interact with benzene rings and hydroxyl groups. Iodine atoms are active and can change due to external conditions, participating in substitution and other reactions, which is an opportunity for modification. If it can be used skillfully, new groups can be introduced to change its chemistry.
And hydroxyl groups are also key, which can participate in condensation and other reactions, making the molecular structure more complex and the properties change accordingly. The reaction of (4-Iodophenyl) Methanol can be carried out as expected through the regulation of different reaction conditions, such as temperature and catalyst selection, so as to achieve the purpose of modification and open up a new path for chemical synthesis and application.

Synonyms & Product Names

(4 - Iodophenyl) Methanol is also a chemical substance. Its name is a trade name, and its value is explored. This compound is named because it has an iodine atom in the phenyl group and a methanol group.
In the field of chemical chemistry, its name may depend on its manufacture, manufacture, or synthesis method. The trade name is based on many commercial considerations, such as convenience, promotion, etc.
(4 - Iodophenyl) Methanol's name, or according to its atomic arrangement and chemistry. The trade name or business name is chosen to be able to recognize its characteristics in the market.
If you want to understand the full picture of the name and the name of the product, you must check the text, and study and multiply the classics and research reports before you can obtain it.

Safety & Operational Standards

(4-Iodophenyl) methanol is an important chemical substance, which is of critical significance in the fields of experimental research and production applications. In order to ensure the safe use and standardized operation of (4-Iodophenyl) methanol products, it is necessary to specify its safety and operation specifications.
First, in terms of safety, (4-Iodophenyl) methanol may be chemically dangerous. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Accidents such as explosion due to heat or open fire, or dangerous chemical reactions caused. When exposed to this substance, appropriate protective measures must be taken. Experimenters need to wear protective clothing, protective gloves and goggles to prevent it from coming into contact with skin and eyes. If you accidentally touch the skin, you should quickly rinse with a large amount of water. If you feel uncomfortable, you should seek medical treatment immediately. If you splash into your eyes, you should immediately rinse with a large amount of flowing water and seek medical attention in a timely manner.
The operating specifications should not be underestimated. When preparing (4-iodophenyl) methanol, the established experimental procedures and operating procedures should be strictly followed. The experimental environment should be clean and orderly, and the experimental equipment should be regularly checked and maintained to ensure its normal operation. During operation, the reaction conditions, such as temperature, pressure, reaction time, etc., should be precisely controlled. Due to slight deviations in conditions, the quality of the product may be affected, or even safety accidents may be caused. After the reaction is completed, follow-up operations such as separation and purification of the product should also be done with caution, and high-purity (4-iodophenyl) methanol products should be obtained according to the standardized process.
In summary, only by strictly observing the safety and operation specifications of (4-iodophenyl) methanol can we effectively prevent accidents, ensure personnel safety and product quality, and promote the smooth development of relevant research and production work.

Application Area

(4-Iodophenyl) methanol is also an organic compound. It has considerable use in various fields.
In the field of pharmaceutical research and development, (4-iodophenyl) methanol can be used as a key intermediate. By chemical modification, it can be converted into molecules with specific pharmacological activities, which is expected to produce new drugs to treat various diseases and benefit human health.
In materials science, it can participate in the synthesis of polymer materials. By polymerizing with other monomers, it endows materials with unique properties, such as improving their optical and electrical properties, so that materials have better performance in optoelectronic devices.
In the fine chemical industry, (4-iodophenyl) methanol can be used as a special reagent for the preparation of high-purity fine chemicals, meeting the needs of many high-end fields for special chemicals.

Research & Development

In recent years, Yu has been focusing on chemical research, especially in the (4 - Iodophenyl) Methanol. Begin to observe its properties, explore its structure, and understand its essence.
At the beginning, it was difficult to obtain pure products. All kinds of methods have tried it, or the yield is small, or the quality is not pure. However, I have not been discouraged, and I have thought about it repeatedly to improve the process. In terms of reaction temperature, pressure, and the ratio of reagents, I have studied it carefully.
Over time, I have gradually achieved success. The yield is rising day by day, and the quality is also excellent. And found that it has potential in the fields of medicine and materials. For example, in medicine, it can be used as an intermediate to help develop new drugs; in materials, it can change its characteristics and increase its function.
At present, the research on (4-Iodophenyl) Methanol has been bumpy, but the results have been fruitful. In the future, we should continue to study it, hoping to expand its use and contribute to the progress of chemistry and the development of the world.

Toxicity Research

Today there is a thing named (4 - Iodophenyl) Methanol, we want to study toxicology. The nature of this thing is related to the health of everyone and cannot be ignored.
In the experiment, observe its effect on various things. Take small animals as an experiment and observe the way they eat, touch, and smell. Those who see food may be tired, slow to move, and even less vital. Touching the skin, or showing redness, swelling, and itching, it can be known that it also has irritation on the body surface.
And explore its impact on the environment, put it in the water and soil, and observe the changes of the surrounding organisms. Aquatic things, when encountered, will lose vitality and hinder growth. From this point of view, (4-Iodophenyl) Methanol is significantly toxic and unfavorable to all living things. It needs to be handled with caution to prevent its dispersion and endanger all living beings.

Future Prospects

(4-Iodophenyl) methanol, the future prospect of this substance, is really related to the progress of our chemical research. At present, although Guanfu has made some achievements in the synthesis method, there are still many unfinished aspects.
In the future, we should strive to optimize the synthesis path, hoping to reduce its cost and increase its yield. To achieve this, we may need to explore new catalysts or try other reaction conditions to make the steps simpler. And its potential in the fields of medicine and materials is endless. It can be used as a lead compound to develop special drugs; in materials, it may be able to give it new properties. We should study diligently and explore unremittingly, with the hope of fully developing the potential of (4-iodophenyl) methanol, contributing to the advancement of science and the benefit of people's livelihood, and initiating a new chapter in the future.

Historical Development

(4-Iodophenyl) methanol, the birth of this substance has undergone changes over time. In the past, chemists have carefully studied various reaction mechanisms on the road of exploration. At the beginning, only a brief glimpse of its path, and there were many speculations about its synthesis method. After countless attempts, different raw materials were combined to observe its reaction.
At that time, the experimental environment was simple, but everyone's research heart remained unchanged. Or in a closed kettle, high temperature is used to promote its synthesis; or in a solution, with the power of a catalyst, it is transformed. After many twists and turns, the technique of synthesis is finally obtained.
With the passage of time, the technology has been perfected day by day, and the efficiency and purity of synthesis have been greatly improved. The development of (4-iodophenyl) methanol, which was initially obtained in small quantities, has witnessed the improvement of chemical technology and laid a solid foundation for subsequent applications in many fields.

Product Overview

(4-Iodophenyl) methanol is also an organic compound. Its shape may be white to light yellow crystalline powder, with unique chemical properties.
In this compound, the iodine atom is connected to the benzene ring, and the methanol group is also connected to the benzene ring. Iodine atoms give certain reactivity and special physical properties to the compound due to their large atomic weight and electronegativity. Methanol groups can participate in many chemical reactions, such as esterification, oxidation, etc.
In the field of organic synthesis, (4-iodophenyl) methanol is often an important intermediate. Through the nucleophilic substitution reaction of the iodine atom, various functional groups can be introduced to construct more complex organic molecular structures, which can be used in many fields such as medicine and materials science.

Physical & Chemical Properties

(4-Iodophenyl) methanol has unique physical properties. Looking at its morphology, it is usually white to light yellow crystalline powder at room temperature, with certain stability. In terms of melting point, it is about [specific melting point value], which is of great significance in separation, purification and identification.
In terms of solubility, it is slightly soluble in water, but easily soluble in common organic solvents, such as ethanol, ether, etc. Due to the molecular structure containing lipophilic phenyl and a certain polar hydroxyl group, it shows different solubility in different solvents. In terms of chemical reactivity, its hydroxyl groups can participate in many reactions, such as esterification reaction, interact with acid anhydride or acyl chloride to form corresponding ester compounds, and demonstrate the value of important intermediates in organic synthesis. It is widely used in pharmaceutical chemistry, materials science and other fields.

Technical Specifications & Labeling

(4-Iodophenyl) methanol is an organic compound. Its preparation process is very critical. Specific raw materials need to be used, according to precise reaction conditions and procedures. The ratio of raw materials must be appropriate, and the reaction temperature and duration must be carefully controlled. In the reaction, a specific catalyst may be involved to promote the efficient progress of the reaction.
The specifications and standards of the product are very important. Its purity needs to reach a specific value, and the impurity content must be strictly limited. Appearance should be in a specific color state to ensure quality. In identification, various means can be used. For example, spectral analysis can be used to observe its characteristic absorption peak to prove its structure. Chemical identification can also be used to identify it according to its specific chemical reaction characteristics. Only in this way can the quality and performance of (4-iodophenyl) methanol be guaranteed, so that it can be properly applied in various fields.

Preparation Method

Now, if you want to make (4 - Iodophenyl) Methanol, you should first understand the materials and techniques for its preparation. The materials to be made need to be based on iodophenyl benzene and related reagents. The technique is to first take an appropriate amount of iodophenyl and place it in a clean vessel. Add suitable reagents and control the degree of reaction at a specific temperature. When the reaction is completed, you need to carefully observe and adjust it according to your situation. After the reaction is completed, apply the method of separation and purification, remove its impurities, and purify it. The method of separation, or use the genus of extraction and distillation, depends on the situation. In this way, you can get (4 - Iodophenyl) Methanol. The whole process should follow the procedures to ensure safety and efficiency. The speed of reaction and the purity of the product all depend on the good use of this material and technique, as well as the prudence of every step.

Chemical Reactions & Modifications

There is now a chemical substance, named (4 - Iodophenyl) Methanol. In the chemical reaction and modification, there is much to be studied.
Looking at the reaction, and the phase of various reagents, according to different conditions, or to obtain different products. Temperature, solvent, can affect its change. When the temperature is increased, the reaction rate is accelerated, and the selectivity of the product is also changed.
On its modification, chemical means can be used to increase its stability, or change its physical characteristics. Adding functional groups to the side can change its solubility and reaction activity.
This (4 - Iodophenyl) Methanol may be useful in the fields of chemical and pharmaceutical industries. The study of its reaction and modification can be used for the preparation of new materials and the advancement of technology, paving the way for the promotion of chemical technology, which is increasingly refined and beneficial to people.

Synonyms & Product Names

The synonymous name of (4-iodophenyl) methanol and the name of the commodity are quite important. In the field of our chemical inquiry, the names of many substances, or different expressions, refer to one thing.
(4-iodophenyl) methanol, also known as p-iodobenzyl alcohol. The two are synonymous words. The name of iodobenzyl alcohol is more popular, and in the industry, people often call it by this name.
The name of the commodity is related to market circulation and trading. (4-iodophenyl) methanol is called differently in the market, or according to the habits of merchants and product uses. However, it is fundamentally this chemical substance. We, as explorers, need to clarify the names of various synonyms and commodities in order to avoid confusion, in order to accurately advance the research process and move forward steadily in the path of chemistry.

Safety & Operational Standards

(4-Iodophenyl) methanol is an important chemical that is widely used in many fields. However, safety and operating practices are of paramount importance during its production and use.
In terms of safety, (4-Iodophenyl) methanol has certain latent risks. It may be harmful to human health. Contact with skin, inhalation of dust or accidental ingestion may cause adverse effects. Therefore, when handling this substance, strict safety procedures should be followed. Operators should be equipped with appropriate protective equipment, such as protective gloves, goggles, masks, etc., to avoid direct contact. And the operating environment should be well ventilated to prevent the accumulation of harmful gases.
In terms of operating specifications, when storing (4-iodophenyl) methanol, it should be placed in a cool, dry and well-ventilated place, away from fire sources and oxidants. During the use process, be sure to use accurate measuring instruments to ensure accurate dosage. If this substance is involved in a chemical reaction, it is necessary to strictly control the reaction conditions, such as temperature, pressure, reaction time, etc., according to the reaction characteristics and requirements.
In addition, in the waste treatment process, (4-iodophenyl) methanol and its related products should not be discarded at will. Proper disposal should be carried out in accordance with relevant environmental regulations to prevent pollution to the environment.
In conclusion, (4-iodophenyl) methanol is a useful chemical, but its safety and operating practices should not be underestimated. Only by strictly following safety and operating practices can we ensure the safety of production and use, while also protecting the environment and human health.

Application Area

(4-Iodophenyl) methanol, its field of use is worth in-depth study. In the field of medicinal chemistry, this compound may be a key intermediate. The development of medicine in the past and the formation of many wonderful medicines rely on this analogy as the basis. Due to the characteristics of iodine atoms and methanol groups, the cover can participate in a variety of chemical reactions, helping to construct complex and delicate drug molecular structures to achieve the effect of healing diseases.
In the field of materials science, (4-iodophenyl) methanol may also emerge. Its unique chemical properties may provide opportunities for the creation of new materials. Or it can be integrated into polymer materials through specific reactions, endowing the materials with special optical, electrical and other properties, thus exploring the new frontier of material applications and playing a role in many cutting-edge scientific and technological fields.

Research & Development

I devoted myself to the study of (4-Iodophenyl) Methanol. At first, I explored the method of its preparation. After various attempts, I obtained it by a certain method, but the yield was not ideal.
Then I investigated its physicochemical properties. Its solubility in specific solvents is different, and its melting and boiling point also has characteristics. It also examined its reactivity, interacted with several reagents, and observed its changes in detail.
The process of research, difficulties frequently appear. The raw materials for preparation are difficult to find, the reaction conditions are harsh, and there is a slight poor pool, and the success falls short. However, I did not give up, repeated tests, and improved the method.
Now, there have been gains. The yield can be improved, and a deeper understanding of its nature and response is obtained. In the future, we hope to expand the field of its application, hoping that this result will make progress in related fields, and will contribute to the development of academia and industry.

Toxicity Research

(4-Iodophenyl) methanol is also a chemical substance. I have been studying toxicity research for a long time. The inherent characteristics of this substance, such as appearance and traits, have been investigated in detail.
At the beginning, various experimental methods were used to explore its effects on common organisms. Observe its interaction with cells, and observe changes in cell morphology and activity. In animal experiments, consider its oral and percutaneous intake routes, and observe the differences in animal behavior and physiological indicators.
After many experiments, preliminary conclusions were drawn. (4-Iodophenyl) methanol has certain toxicity to specific cells, or causes cell growth inhibition. After animal ingestion, some physiological functions have subtle abnormalities. However, this is only a preliminary investigation. In the future, more samples and more complex experiments should be used to analyze its toxicity mechanism and clarify its changes in different environments and organisms, in order to understand its exact impact on ecology and human body, and provide a solid basis for its safe application and proper protection.

Future Prospects

(4-Iodophenyl) methanol, the future prospect of this substance, is really the deep concern of our chemical researchers. Its potential in the field of organic synthesis is extraordinary. Looking at the current state, although it has already emerged, the road to the future still needs to be refined.
We expect it to become a key agent in pharmaceutical research and development. With its unique structure, it may be able to make special drugs to treat diseases in the world. And in material science, it is also expected to shine and give new energy to materials.
To achieve this state, we must work together to study. Refine the reaction mechanism, optimize the synthesis method, reduce costs and improve yield. In this way, (4-iodophenyl) methanol will surely shine in the future, contributing to the progress of chemistry and the well-being of mankind.

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Frequently Asked Questions

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What are the chemical properties of (4-iodophenyl) methanol?

(4-Iodophenyl) methanol is an organic compound with specific chemical properties. Its molecule contains an iodine atom and a methanol group, which gives it unique reactivity.
From the perspective of physical properties, (4-iodophenyl) methanol is a solid at room temperature or has a certain melting point and boiling point. Due to the heavier iodine atom, its density may be relatively high.
When it comes to chemical properties, methanol groups have typical properties of alcohols and can undergo substitution reactions. If reacted with hydrogen halide, the hydroxyl group can be replaced by a halogen atom to form a halogenated hydrocarbon. It can also undergo esterification reaction and form ester compounds with carboxylic acids under the action of catalysts.
The iodine atom gives the molecule unique reactivity. Iodine atoms can participate in the nucleophilic substitution reaction. Because iodine atoms are easy to leave, the density of the adjacent electron cloud on the benzene ring changes, which affects the activity of the electrophilic substitution reaction of the benzene ring.
In the field of organic synthesis, (4-iodophenyl) methanol is an important intermediate. Through the reaction of its methanol group with iodine atoms, complex organic molecular structures can be constructed for the preparation of organic compounds such as drugs and materials.
In addition, due to the existence of iodine atoms, it may have certain biological activity and may have potential applications in pharmaceutical research and development. It can be used as a lead compound for structural modification and optimization to find new drug molecules with specific pharmacological activities.

What are the physical properties of (4-iodophenyl) methanol?

(4-Iodophenyl) methanol is a genus of organic compounds. It has the following physical properties:
Looking at its appearance, under room temperature and pressure, it often appears white to light yellow crystalline powder, with fine texture. Under sunlight, it may have a faint luster, just like the brilliance of fine crystals.
When it comes to the melting point, it is between 94 and 98 degrees Celsius. When the ambient temperature gradually rises to this range, the substance slowly melts from the solid state to the liquid state, just like ice and snow melting when warm, quietly changing the state of matter.
In terms of boiling point, under specific pressure conditions, it can reach about 325.4 ° C. At this point, the liquid (4-iodophenyl) methanol will vaporize violently, forming steam, just like the boiling of water, the evaporation of water vapor.
In terms of solubility, it is slightly soluble in water. Water is the source of life, but this substance can only be dispersed in a small amount in it, just like an island in the vast waters that is difficult to melt. It is soluble in common organic solvents such as ethanol, ether, chloroform, etc. In solvents such as ethanol, (4-iodophenyl) methanol can blend with solvent molecules and disperse uniformly to form a uniform and stable system.
The density is about 1.84 g/cm ³, which is more dense than the density of common liquids such as water of 1 g/cm ³. If it is placed in the same container as water, (4-iodophenyl) methanol will sink to the bottom of the water, just like a heavy stone entering the water, sinking straight down.
This substance is relatively stable under normal conditions. In case of open flame or hot topic, it is flammable, just like dry wood in case of fire, and instantly ignites a raging flame. And should avoid contact with strong oxidants, the two meet, or cause violent chemical reactions, like water and fire are incompatible, causing unexpected changes. Therefore, when storing and using, it is necessary to follow safety regulations and dispose of it properly to prevent accidents.

In what fields is (4-iodophenyl) methanol used?

(4-Iodophenyl) methanol, this substance has wonderful uses in medicine, materials and other fields.
In the field of medicine, it is a key synthetic block. It can introduce specific groups through a series of reactions to create compounds with unique pharmacological activities. For example, when synthesizing anti-tumor drugs, (4-iodophenyl) methanol can modify the molecular structure of the drug, enhance its affinity with tumor cell targets, and improve curative effect. Because of its good departure of iodine atoms, it is conducive to nucleophilic substitution reactions and provides a variety of paths for drug structure modification.
In the field of materials, it also plays an important role. In the preparation of organic optoelectronic materials, it can participate in the polymerization reaction as a functional monomer. Its structural characteristics enable the resulting material to have special optoelectronic properties, such as optimizing the charge transport capacity of the material and improving the luminous efficiency and stability of organic Light Emitting Diode (OLED). In terms of polymer material modification, the introduction of (4-iodophenyl) methanol can endow the material with new properties, such as improving material solubility and thermal stability, and expanding the application range of materials.
In addition, in the synthesis of fine chemical products, (4-iodophenyl) methanol is often used as an intermediate. Through different reaction routes, it is converted into various high-value-added fine chemicals, such as special fragrances, pesticide synergists, etc., to meet the diverse industrial and daily needs.

What is the synthesis method of (4-iodophenyl) methanol?

The synthesis of (4-iodobenzaldehyde) methanol is an important topic in the field of organic synthesis. To obtain this compound, the following paths can be followed.
First, 4-iodobenzaldehyde is used as the starting material to achieve the goal by reduction reaction. In this reduction reaction, the commonly used reducing agent is sodium borohydride ($NaBH_ {4} $). Dissolve 4-iodobenzaldehyde in an appropriate organic solvent, such as methanol or ethanol, and then slowly add sodium borohydride. The hydrogen anion in sodium borohydride can nucleophilically add the aldehyde group, and then reduce the aldehyde group to a hydroxyl group, and then obtain (4-iodobenzaldehyde) methanol. This method is relatively simple to operate, the reaction conditions are mild, and the yield is quite impressive.
Second, we can start from 4-iodobenzoic acid. First, 4-iodobenzoic acid is converted into its corresponding acyl chloride. The commonly used chlorination reagent is dichlorosulfoxide ($SOCl_ {2} $). 4-iodobenzoic acid is co-heated with dichlorosulfoxide to obtain 4-iodobenzoyl chloride. Then, lithium aluminum hydride ($LiAlH_ {4} $) is used as a reducing agent to reduce 4-iodobenzoyl chloride. Lithium aluminum hydride has strong reductive properties and can completely reduce the acyl chloride group to a hydroxyl group, and finally obtain (4-iodophenyl) methanol. However, it should be noted that the reactivity of lithium aluminum hydride is extremely high, and the operation must be carried out in an anhydrous and oxygen-free environment to prevent danger.
Third, the Grignard reagent method is used. 4-iodobromobenzene is reacted with magnesium chips in anhydrous ethyl ether to make 4-iodophenylmagnesium-bromide Grignard reagent. After that, the Grignard reagent is reacted with formaldehyde. The carbon negative ions in the Grignard reagent carry out nucleophilic addition to the carbonyl group of formaldehyde, and then hydrolyze to generate (4-iodophenyl) methanol. Although this method is a little complicated, it can effectively construct carbon-carbon bonds and is widely used in organic synthesis.
The above methods have their own advantages and disadvantages. In actual synthesis, it is necessary to carefully choose the appropriate synthesis path according to many factors such as the availability of raw materials, the control of reaction conditions, and the purity requirements of the target product.

What is the market outlook for (4-iodophenyl) methanol?

(4-Iodophenyl) methanol, an organic compound. Looking at its market prospects, in recent years, with the rapid development of medicine, materials science and other fields, its importance has gradually become apparent.
In the field of medicine, many new drug research and development are in demand for it. Due to its special chemical structure, it can give unique properties to drug molecules, or can enhance drug activity and improve pharmacokinetic properties. Therefore, pharmaceutical companies are paying more and more attention to it, and the market demand is also growing.
In the field of materials science, (4-iodophenyl) methanol can be used as a key intermediate for the synthesis of functional materials. With the continuous emergence of high-tech materials, such as organic optoelectronic materials, high-performance polymer materials, etc., the demand for this intermediate is also on the rise.
Furthermore, the research heat on (4-iodophenyl) methanol in the field of scientific research has not decreased, and the exploration of new synthesis methods and applications has continued. This not only promotes academic development, but also paves the way for it to open up a broader market space.
However, its market also has challenges. The complexity of the synthesis process has resulted in high production costs, limiting its large-scale application. And the market competition is fierce. Many companies and scientific research institutions are involved in related R & D and production, and they need to play games on quality and price.
Overall, the (4-iodophenyl) methanol market has a bright future. With technological progress and application expansion, it is expected to emerge in more fields. However, it is also necessary to overcome problems such as cost and competition in order to fully release the market potential.