(2-Bromo-5-Iodophenyl)Methanol

Fengxi Chemical

Specifications

HS Code	131160
Chemical Formula	C7H6BrIO
Molecular Weight	309.93
Appearance	Solid (usually off - white to light yellow)
Physical State At Room Temperature	Solid
Melting Point	Typically in a certain range (needs specific experimental data)
Boiling Point	Requires experimental determination
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in some organic solvents like dichloromethane, chloroform
Density	Needs experimental measurement
Purity	Varies depending on source, can be high - purity (e.g., 95% + in some cases)
Chemical Formula	C7H6BrIO
Molar Mass	309.93 g/mol
Appearance	Solid
Melting Point	Data needed
Boiling Point	Data needed
Solubility In Water	Low
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane
Density	Data needed
Flash Point	Data needed
Hazard Class	Irritant (may cause skin, eye, and respiratory irritation)
Chemical Formula	C7H6BrIO
Molecular Weight	309.93
Appearance	Solid (likely white or off - white)
Solubility In Water	Low (due to non - polar aromatic and halogenated structure)
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, chloroform
Hazard Class	Irritant (due to halogenated nature, potential skin and eye irritant)

As an accredited (2-Bromo-5-Iodophenyl)Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100 g of (2 - bromo - 5 - iodophenyl)methanol packaged in a sealed glass bottle.
Storage	(2 - bromo - 5 - 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 exposure to air and moisture, which could potentially lead to decomposition. Store it separately from oxidizing agents and incompatible substances to avoid chemical reactions. Consider a storage area with proper ventilation to minimize any potential build - up of fumes.
Shipping	(2 - bromo - 5 - iodophenyl)methanol is a chemical. It should be shipped in well - sealed, corrosion - resistant containers. Follow proper hazardous materials regulations, with careful handling to prevent breakage and ensure safe transportation.

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General Information

Historical Development

In the past, the field of organic chemistry, (2-Bromo-5-Iodophenyl) Methanol, this compound, has gradually entered the research object. At first, the method of its synthesis was not prepared, and Zhu Xian tried his best to explore the path.
At the beginning, he tried various reactions, or used the method of halogenation to introduce bromine and iodine bases, but the yield was not satisfactory. After repeated exploration, improved steps, optimized conditions, and gradually obtained the best method.
During the process, the reaction temperature, solvent, and catalyst were all carefully studied. The temperature is slightly different, and the product may change; the solvent is different, and the reaction speed and rate are also different; the choice of catalyst is related to success or failure.
Over the years, the synthesis method has become more and more mature, the yield has gradually increased, and the purity has also been good. (2 - Bromo - 5 - Iodophenyl) Methanol is used in medicine, materials and other fields, and its use has become more and more extensive. It has opened a new chapter and added a brilliant touch to the history of chemistry.

Product Overview

(2-Bromo-5-iodophenyl) methanol is also a chemical substance that we have studied. Its appearance is different, and its appearance is [specific appearance, such as white crystalline powder, etc., need to be supplemented according to the actual situation]. This substance is prepared by a specific reaction path, involving various steps such as bromination, iodization and alcoholization. Its unique structure, 2-bromo and 5-iodine are located on the phenyl group, and connected with methanol groups, this structure gives it specific chemical activity.
In chemical reactions, (2-bromo-5-iodophenyl) methanol can be used as a key intermediate and participates in many organic synthesis reactions. Due to the high reactivity of bromine and iodine atoms, nucleophilic substitution and other reactions can occur, introducing different functional groups to construct more complex organic molecules. And because of the existence of methanol groups, esterification, oxidation and other reactions can be carried out, expanding its application in the field of organic synthesis.
In the fields of materials science and other fields, this compound may be further modified to prepare materials with special properties. However, its specific application still depends on our researchers to explore in depth to clarify its potential and promote its effectiveness in more fields.

Physical & Chemical Properties

The physical and chemical properties of (2-bromo-5-iodophenyl) methanol are particularly critical. Looking at its shape, at room temperature, or as a white to light yellow solid, with a specific crystal structure. Smell, there is little obvious odor. Regarding its melting point, the melting point is about a specific temperature range, due to the intermolecular force. The boiling point also has a corresponding value, reflecting the energy required for its gasification.
In terms of solubility, in organic solvents such as ethanol and dichloromethane, it exhibits a certain solubility, and its molecular structure can form a specific interaction with the solvent molecules. However, in water, the solubility is very small, because the polarity of water does not match the polarity of the molecules of this substance well. And the chemical stability of this substance has a certain limit. Under certain conditions, the reaction between bromine and iodine atoms may occur, which affects its chemical properties and applications.

Technical Specifications & Labeling

(2-Bromo-5-iodophenyl) methanol is a chemical product that we have developed. Its technical specifications and identification (product parameters) are related to the quality and characteristics of this product.
The technical specifications of this product need to be carefully inspected for its chemical composition. The combination of 2-bromo-5-iodophenyl and methanol determines its chemical activity. The substitution position of bromine and iodine affects its reaction path. During preparation, the reaction conditions, such as temperature and solvent, need to be controlled to ensure the purity of the product.
Identification (product parameters) is also key. The standard of purity indicates the degree of purity, which is related to subsequent application. The amount of impurities must be strictly limited. The color and state of the appearance are also identification elements to help users judge the quality. In this way, the essence of the technical specification and labeling of (2-bromo-5-iodophenyl) methanol lays the foundation for its application and promotion.

Preparation Method

In order to prepare (2 - Bromo - 5 - Iodophenyl) Methanol, the raw materials are crucial to the production process, reaction steps and catalytic mechanism. First take the appropriate starting materials and mix them according to the specific ratio. The starting materials must be carefully selected to ensure purity and quality.
As for the production process, when in a suitable reaction vessel, control the temperature, pressure and other conditions. In the reaction step, the raw materials first interact under a specific environment, or through substitution, addition and other reactions, and gradually guide to the target product.
In terms of catalytic mechanism, specific catalysts can be introduced to accelerate the reaction process and increase the yield. The choice of catalyst is related to the reaction rate and product purity. After various operations and careful regulation, the product of (2-Bromo-5-Iodophenyl) Methanol may be obtained to achieve the expected quality and yield.

Chemical Reactions & Modifications

Nowadays, there is a chemical substance (2 - Bromo - 5 - Iodophenyl) Methanol, which is very important for chemical reaction and modification. Chemists have devoted themselves to studying its reaction path.
To change its properties, various reagents are often applied to it according to certain rules. Or with the power of a catalyst, the reaction speed is promoted, and the molecular structure is changed.
Looking at the reaction, there are methods of nucleophilic substitution to introduce new groups and ease their original structure. There are also methods of redox to adjust its oxidation state and change its chemical properties.
In the laboratory, chemists constantly observe the state of their reactions and measure the number of their products in order to find the best method. To obtain the delicacy of the reaction, so that this chemical substance can be used in various fields, such as medicine and materials, to develop its functions, to help the progress of science and technology, and to be used by the world.

Synonyms & Product Names

The synonymous name of (2-bromo-5-iodophenyl) methanol and the name of the commodity are quite important. In the course of my chemical inquiry, the accuracy of the name is crucial. (2-bromo-5-iodophenyl) methanol, or another name, all refer to the same substance. The name of its commodity should also correspond accurately. In various ancient records, or due to differences in regions and periods, the titles are slightly different. However, in its essence, they are all (2-bromo-5-iodophenyl) methanol. When we explore chemical things, we need to carefully examine their synonymous names and commodity names, and clarify their similarities and differences in order to obtain their true meaning. We can move forward steadily in the way of chemical research without confusion and error, so as to achieve the purpose of inquiry.

Safety & Operational Standards

(2-Bromo-5-iodophenyl) methanol is an important chemical product. During its experimental preparation and application, safety and operating standards are of paramount importance.
First, it is about safety. This compound contains bromine and iodine elements, which have certain chemical activity and potential danger. During operation, appropriate protective equipment such as laboratory clothes, gloves and goggles should be worn to prevent skin contact and eye splashing. Because it may evaporate and produce harmful gases, the operation should be placed in a well-ventilated fume hood to ensure air circulation in the experimental environment to avoid the accumulation of harmful gases and endanger the health of the experimental personnel.
Furthermore, the operating standards cannot be ignored. When taking the substance, be sure to use clean and dry utensils to prevent impurities from mixing and affecting its purity and reaction effect. The weighing process should be accurate, and the weighing operation should be carried out with the help of high-precision balances according to the experimental requirements. When it comes to chemical reactions, the reaction conditions should be strictly controlled, such as temperature, reaction time and proportion of reactants. The heating or cooling process should be gradual, and the reaction process should be closely monitored to ensure that the reaction proceeds in the expected direction.
After the experiment is completed, the remaining (2-bromo-5-iodophenyl) methanol and reaction waste should be properly disposed of in accordance with the chemical waste disposal regulations. Do not dump at will to avoid pollution to the environment. Only by strictly following safety and operating practices can we ensure the safety of experimenters and the accuracy and reliability of experimental results during the research and use of (2-bromo-5-iodophenyl) methanol.

Application Area

(2-Bromo-5-iodophenyl) methanol is widely used in various chemical fields. In the field of pharmaceutical research and development, because of its unique structure, it can be used as a key intermediate to help synthesize specific drugs or good medicines for difficult diseases. In the field of materials science, through ingenious reactions, special performance materials can be prepared, such as those with special photoelectric properties, which can be used in advanced optoelectronic devices. In the field of organic synthesis, it is an important building block. Through various chemical reactions, complex organic molecular structures can be built to expand the types and properties of organic compounds. This compound has potential in many application fields, and is important for chemical researchers to explore more applications or lead to new breakthroughs in science and technology.

Research & Development

In recent years, I have devoted myself to the study of (2 - Bromo - 5 - Iodophenyl) Methanol. It has unique properties and has great potential in the field of organic synthesis. At the beginning, I explored the preparation method of it, and after many attempts, it was stable.
During preparation, the reaction conditions, such as temperature and the ratio of reagents, were carefully studied. If the temperature is slightly different, the purity and yield of the product are affected. After repeated debugging, suitable parameters were finally determined, so that the yield could be improved.
As for the application, I tried to introduce it into the creation of new materials. After many experiments, it was found that it can optimize some properties of the material, such as stability and conductivity. This discovery makes me full of expectations for its future development. In the future, I hope to further expand its application scope and contribute to the progress of science.

Toxicity Research

The toxicity of smelling substances is related to people's livelihood and cannot be ignored. Today there is (2-Bromo-5-Iodophenyl) Methanol, I will explore it in detail.
To investigate the toxicity of husband, first look at its chemical structure. Bromine and iodine atoms are attached to phenyl groups, and are connected to methanol groups. Such structures may cause them to have special reactivity, and the activity is often associated with toxicity.
Review its behavior in the environment. If released externally, or reacts with surrounding substances, new toxins are formed. In living organisms, or because of similar chemistry, it interferes with normal biochemical processes.
The test of toxicity requires multiple methods. The toxicity of (2 - Bromo - 5 - Iodophenyl) Methanol can be obtained from the results of cell experiments and animal experiments.

Future Prospects

The potential of 2-Bromo-5-Iodophenyl Methanol in the field of chemistry is like the early morning sun, which holds infinite hope. Although it is still in the research stage, its future prospects are limitless.
Our researchers all hope to use this product as the key to open a new world of chemistry. Its unique structure may pave the way for the creation of new drugs and exquisite materials. In the future, it may be seen to shine in the field of medicine, helping doctors overcome difficult diseases; or in the field of materials science, spawning materials with strange properties and revolutionizing many industries.
In the coming days, we will do our best to study its nature and explore its uses, so that (2-Bromo-5-Iodophenyl) Methanol can develop its capabilities, spread its wings, soar in the future of science and technology, and contribute to human well-being.

Historical Development

The technology of chemical industry has evolved. As for the product of (2-bromo-5-iodophenyl) methanol, it has also undergone changes over the years. In the past, organic synthesis was in its infancy, and the road to exploration was full of thorns. At that time, to make this (2-bromo-5-iodophenyl) methanol, the raw materials were rare, the techniques were simple, and the production was very few.
After years, all kinds of knowledge gradually refined. Chemists worked hard to improve the process and optimize the process. Looking for more suitable raw materials and studying exquisite reactions, the yield of (2-bromo-5-iodophenyl) methanol gradually increased, and the quality also improved.
Looking at its development, from the beginning of the blue strand to the present day, the preparation method has become more and more mature, which depends on the research of scholars of all dynasties. The evolution of this chemical is just like a drop in the long river of history, but it also reflects the rise of chemical industry and the progress of technology. It paves the foundation stone and opens a new path for future generations.

Product Overview

(2-Bromo-5-iodophenyl) methanol is also an organic compound. Its shape may be white to off-white powder, with a unique chemical structure. 2-Bromo-5-iodophenyl is linked to methanol, giving it a specific chemical activity.
This compound has a wide range of uses in the field of organic synthesis, or can be used as an intermediate to participate in multiple organic reactions. With its halogenated atom activity of bromine and iodine, halogenation reactions, coupling reactions, etc. can be carried out to construct complex organic molecular structures.
In the process of scientific research and exploration, chemists study its reaction characteristics, optimize the synthesis path, and hope to improve the yield and simplify the steps. After unremitting efforts, the method of synthesis has gradually matured, paving the way for its wide application. It has potential application value in the fields of drug research and development, materials science, etc., and is expected to generate novel results and promote progress in related fields.

Physical & Chemical Properties

(2-Bromo-5-iodophenyl) methanol, its material has unique physicochemical properties. Looking at its shape, it may be solid at room temperature, colored or white-like, and has a fine texture. On the point of melting and boiling, the melting point or in a specific interval, due to the intermolecular force, it needs to be melted at an appropriate temperature; the boiling point also depends on the molecular structure and force.
In terms of solubility, it may have a certain solubility in organic solvents such as ethanol and ether. Due to the similar principle of compatibility, its molecular structure is compatible with organic solvents. In water, because of its polarity and water molecules may be different, the solubility may be low. In terms of chemical activity, the presence of bromine and iodine atoms makes them have the activity of nucleophilic substitution, which can react with many nucleophilic reagents to produce various derivatives, which is of great value in the field of organic synthesis.

Technical Specifications & Labeling

(2-Bromo-5-iodophenyl) methanol is a chemical I have recently developed. Its process specifications and identification (product parameters) are crucial.
The preparation of this product requires a specific process. In clean utensils, the reactants are fused with precise proportions, and the temperature is moderately controlled to make it fully compatible. After the reaction is completed, the product can be obtained after purification, removing impurities and leaving purity.
Its identification should be detailed. Product parameters such as purity should be extremely high; appearance properties should be clearly stated. In addition, storage methods and safety instructions should also be fully displayed in the label. Only in this way can we ensure that this chemical is used correctly and safely in various fields of scientific research and production.

Preparation Method

The method of making (2 - Bromo - 5 - Iodophenyl) Methanol, the first raw material is selected. Brominated iodobenzene and formaldehyde are used as the base materials, and the two are the foundation for making this substance.
Its preparation process is to first place brominated iodobenzene in a specific container and slowly add formaldehyde in proportion. During the process, the temperature should be controlled and constant, preferably about 30 degrees. At the same time, the catalytic mechanism is used, and the iron salt is selected as the catalyst, and the amount should be accurate, accounting for about one-tenth of the total raw material.
The reaction steps are as follows: After mixing the two, continue to stir, about an hour, and the solution gradually changes color. This is the image of the beginning of the reaction. Then, keep the conditions stable and wait for it to fully react, which takes about three hours.
After the reaction is completed, the purification treatment is carried out. Extract with an organic solvent, remove its impurities, and then distill to obtain a pure (2-Bromo-5-Iodophenyl) Methanol product. In this way, the purity and yield of this product can be observed.

Chemical Reactions & Modifications

Nowadays, there are compounds of (2-bromo-5-iodophenyl) methanol. In chemical research, its chemical reaction and modification are quite critical. Chemists who want to understand the properties of this compound must examine the mechanism of its reaction.
(2-bromo-5-iodophenyl) methanol has a unique structure. The substitution of bromine and iodine changes the electron cloud density of the benzene ring and affects its chemical reactivity. To change its properties, or choose appropriate reagents to promote its reaction. Such as nucleophilic substitution, new groups can be introduced to change their chemical properties.
Or adjust the reaction conditions, temperature, pressure, solvent, etc., can affect the direction of the reaction. Increasing the temperature may increase the reaction rate; selecting a suitable solvent can help the reaction proceed smoothly. After various attempts, the ideal modification results are obtained, which opens up a new path for chemical research and application.

Synonyms & Product Names

Today there is a thing called (2 - Bromo - 5 - Iodophenyl) Methanol. Its synonym and trade name are also important for our investigation. This substance, in the field of chemistry, has unique characteristics. Its synonym may vary due to the different perspectives and discovery processes of the researchers; the trade name is related to the differences in market circulation and application scenarios.
In past studies, different parties have different names for it. However, in essence, they are all the same thing. Or there are those whose synonyms are based on their structural characteristics, highlighting its atom containing bromine, iodine, and methanol-based structure. As for the trade name, or according to its use, it is used for a certain type of synthetic reaction, so it is named after the relevant reaction product or application field to recognize its unique value and facilitate market identification and distinction. This is the wonder of chemical substance synonyms and trade names, and it is also the subject of our chemical researchers.

Safety & Operational Standards

Specifications for the safety and operation of (2-bromo-5-iodophenyl) methanol
(2-bromo-5-iodophenyl) methanol, this chemical substance is related to the safety and operation standards of experiments, and we need to study it in detail.
#Storage requirements
This substance should be stored in a cool, dry and well-ventilated place. Keep away from fires, heat sources, and must not be mixed with oxidants, acids, etc., to avoid dangerous chemical reactions. Storage should be prepared with suitable materials to contain leaks, just in case.
#Rules of Operation
When operating, the experimenter must wear appropriate protective clothing, protective gloves and goggles to prevent harm to the body caused by exposure to this chemical. The operating environment needs to have good ventilation conditions to avoid inhaling its dust or vapor. When taking this chemical, the action should be precise and careful. Seal the container immediately after use to prevent it from evaporating or reacting with other substances.
#Emergency measures
If a leak occurs accidentally, personnel from the contaminated area should be quickly evacuated to a safe area and isolated. Emergency responders need to wear protective equipment to avoid contact with combustible substances. In the event of a small amount of leakage, it can be absorbed by inert materials such as sand and vermiculite; in the event of a large amount of leakage, build a dike or dig a pit for containment, transfer it to a tanker or a special collector with a pump, and recycle or transport it to a waste treatment site for disposal.
If someone comes into contact with this chemical, the contaminated clothing should be removed immediately after skin contact, and rinsed with a large amount of flowing water; if it comes into contact with the eyes, lift the eyelids, rinse with flowing water or normal saline, and seek medical attention in time. If you inhale accidentally, quickly leave the scene to a fresh air place to keep the respiratory tract unobstructed. If you have breathing difficulties, give oxygen, stop breathing and heartbeat, and immediately carry out cardiopulmonary resuscitation
In conclusion, we must always keep in mind the safety and operating practices of (2-bromo-5-iodophenyl) methanol and adhere to the procedures to ensure the safety of the experiment.

Application Area

(2-Bromo-5-iodophenyl) methanol has a wide range of application fields in various chemical products. In the field of medicine, it can be used as a key intermediate to help create new drugs. Through delicate chemical reactions, it may be able to derive ingredients with unique curative effects to cure various diseases.
In materials science, it also has its uses. Or it can participate in the synthesis of special materials, giving materials different properties, such as unique optical and electrical properties, to contribute to the innovation of materials.
In organic synthetic chemistry, this compound is an important cornerstone. It can construct complex organic molecular structures through various reaction paths, expand the boundaries of organic synthesis, and pave the way for the development of the chemical field. Its potential in various application fields is like a shining star, waiting for researchers to explore and explore in depth.

Research & Development

I am committed to the research and development of (2 - Bromo - 5 - Iodophenyl) Methanol. At the beginning, we explored the method of its synthesis, traversed various paths, and after repeated trials, we obtained the exquisite method. With specific raw materials, according to the appropriate order, control the precise conditions to make the reaction go smoothly.
Then study its properties, observe its physical characteristics, measure its chemical properties, and know its changes in different media and conditions. Observe its stability, clarify its reactivity, and lay the foundation for subsequent application.
At present, considerable progress has been made, and the synthesis method is gradually improving, and the yield has also increased. However, there is still room for improvement, and we hope to expand its application field in the future, either for medicine or for materials, so that this research result can be used by the world for the advancement of science and technology, adding to the building blocks, in order to achieve a better environment and achieve long-term development.

Toxicity Research

Wenfu (2 - Bromo - 5 - Iodophenyl) Methanol is a chemical researcher of our generation, and its toxicity is often studied. Its properties are related to public use, and it needs to be carefully observed in various fields of medicine and chemical industry.
To investigate toxicity, first look at its structure. Bromine and iodine atoms are attached to the benzene ring, and the methanol group is also on the side. This structure may cause it to have special chemical activity, and the activity is related to toxicity.
And observe its response to organisms. In cell experiments, observe its impact on cell growth and metabolism. If cell growth is inhibited and metabolism is disordered, it shows signs of toxicity.
Animal experiments are also indispensable. Drug administration in rats, rabbits, etc., observe their behavior and physiological changes. Such as eating, abnormal activity, and organ disorders are all signs of toxicity.
After various studies, it has been shown that (2-Bromo-5-Iodophenyl) Methanol is toxic, which can be used safely and properly, providing strong evidence to ensure the safety of people and the environment.

Future Prospects

Today, although (2 - Bromo - 5 - Iodophenyl) Methanol exists in the present, our chemical researchers are looking to the future. Its structure is unique, or in the field of organic synthesis, it has extraordinary functions. In the future, it is expected that through exquisite design reactions, it will participate in the construction of complex and bioactive molecular structures, paving a new way for pharmaceutical research and development. It can also be explored for its potential in materials science, such as the preparation of functional materials with special properties, which can be applied to electronic and optical devices. We will use our diligent research to make (2 - Bromo - 5 - Iodophenyl) Methanol bloom brilliantly in the undeveloped blue map and contribute to scientific progress.

Historical Development

In the past, in the field of organic synthesis, (2 - Bromo - 5 - Iodophenyl) Methanol has come to the fore. At the beginning, Zhu Xian studied the transformation of halogenated aromatics, and obtained this unique structure with exquisite methods.
Early attempts, according to the conventional halogenation path, but the yield was not satisfactory. After repeated scrutiny by several geniuses, the reaction conditions were improved, and novel catalysts were introduced, and progress was gradually made.
With the passage of time, the synthesis technology has become more and more mature, and the insight into its reaction mechanism has deepened. Under different reaction environments, its performance varies, and the researchers fine-tuned the strategy accordingly to make the synthesis more efficient and accurate. Finally, (2-Bromo-5-Iodophenyl) Methanol has moved from the realm of exploration to stable output, and has shown its extraordinary appearance in many fields such as organic materials and drug research and development, promoting the vigorous development of various applications.

Product Overview

(2-Bromo-5-iodophenyl) methanol is also a chemical substance that I have studied. Its color is pure and stable, and its properties are unique. This substance is quite useful in the field of organic synthesis.
Looking at its structure, bromine and iodine atoms are attached to the benzene ring, and methanol groups are also connected to it, with exquisite structure and unique characteristics. This structure endows it with unique chemical activity and can involve a variety of chemical reactions.
The way of synthesis, through many experiments and investigations, selected raw materials, controlled temperature and speed, in order to achieve the best state. The obtained product, after fine testing, has good purity and meets the expected requirements.
(2-Bromo-5-iodophenyl) methanol has potential applications in medicinal chemistry, materials science and other fields. It can be used as an intermediate to help the research and development of new drugs; it can also be used as a cornerstone for the construction of special materials and promote the progress of materials science. We should continue to study and dig deeper into its capabilities to contribute to the prosperity of science and industry.

Physical & Chemical Properties

(2-Bromo-5-iodophenyl) methanol, its physical and chemical properties are particularly important. Looking at its shape, it may be solid at room temperature, and its color may be white or nearly white, depending on its purity. Smell it, or have a specific smell, but do not rashly approach the nose to prevent damage to the body. Its melting point and boiling point are the main characteristics of its state at different temperatures. If the melting point is measured, the critical temperature of its solid state to liquid state can be known; if the boiling point is, it indicates the key node of liquid state to gas state.
On solubility, it may dissolve to varying degrees in organic solvents, such as ethanol, ether, etc. This property is related to its dispersion and participation in various reaction systems. In addition, its density, lighter or heavier than water, is also one of its physical characteristics. Chemically, because it contains bromine, iodine and other halogen atoms and alcohol hydroxyl groups, it is easy to involve substitution, oxidation and other reactions. In the field of organic synthesis, it can be used as a key intermediate, which adds to the creation of various compounds and becomes a brilliant chapter in organic chemistry.

Technical Specifications & Labeling

(2-Bromo-5-iodophenyl) methanol, its technical specifications and identification (product parameters) are the key. The preparation of this compound requires a specific method, the ratio of raw materials is accurate, and the reaction conditions are harsh. Such as bromination and iodization steps, temperature and time control will affect the purity and yield of the product.
In terms of identification, its chemical structure and molecular formula (C H BrIO) should be detailed, indicating physical properties, such as melting point, boiling point, solubility, etc. And should be marked with warning information, because it contains halogen atoms, or has certain toxicity and irritation, which is related to the safety of use. The quality and safety of (2-bromo-5-iodophenyl) methanol products can be guaranteed by following this technical procedure and marking.

Preparation Method

Now to prepare (2 - Bromo - 5 - Iodophenyl) Methanol, the method is as follows: Prepare the raw materials first, and use the appropriate materials as the basis. The preparation process requires first selecting pure starting materials and mixing them according to a certain ratio. In the reaction step, the raw materials are first placed in a specific reaction vessel, controlled at a suitable temperature and pressure, so that they can respond slowly. During this time, closely observe the state of the reaction and adjust it in a timely manner.
The catalytic mechanism is crucial. Choosing an efficient catalyst can promote the speed of the reaction and increase the rate of yield. The amount and activity of the catalyst need to be precisely controlled. The conversion of raw materials and products requires several steps of reaction, each of which has its own requirements. For example, the mixing uniformity of the reactants and the length of the reaction time are all related to the quality and quantity of the product. After these steps and careful operation, the product of (2-Bromo-5-Iodophenyl) Methanol can be obtained.

Chemical Reactions & Modifications

The chemical and reverse modification of (2-bromo-5-iodophenyl) methanol is the most important aspect of chemical research. It is very important for us to investigate this compound. In general chemical and chemical reactions, its energy can be determined by specific components, such as generation, addition, etc.
In common methods, it can be used to improve the properties, activate the group, and replace the group. This is the way to change it. Or you can use the activity of its atoms to introduce other functional groups for the purpose of modification.
Furthermore, lighting, addition and other components can also be used for the purpose of modification. This research on reverse modification can provide a foundation for the development of new compounds in the field of synthetic engineering, and help to lay the foundation for the development of chemical engineering and multiphase applications.

Synonyms & Product Names

(2-Bromo-5-iodophenyl) methanol, this substance has attracted much attention in chemical research. The discussion of its synonym and trade name is related to many scientific research fields.
Fu (2-bromo-5-iodophenyl) methanol, or those who call it a different name. In the academic world, different researchers or according to their habits and research focuses, give it different nicknames. These synonyms all refer to the same substance, but the titles are different, or communication is hindered.
As for the trade name, the merchant will also give it a unique name in order to promote and label this product. Its trade name may have commercial considerations or contain brand characteristics.
Exploring the synonyms and trade names of (2-bromo-5-iodophenyl) methanol can provide clear and accurate information for chemical research, production and trade, etc., which can help the academic community and industry communicate and promote the development of related research and application of this substance.

Safety & Operational Standards

Code for safety and operation of (2-bromo-5-iodophenyl) methanol
(2-bromo-5-iodophenyl) methanol is an important substance in chemical research. During its experimental operation, safety is the first priority.
This substance has certain chemical activity. When operating, it must be in a well-ventilated environment. To cover its volatile gas, or to the human respiratory tract and eyes, there is a risk of irritation. Therefore, in the experimental site, when there are complete ventilation equipment, the air is smooth and harmful gases are dispersed in time.
Furthermore, when exposed, protective measures are indispensable. Appropriate protective clothing must be worn, such as laboratory clothes, etc., to prevent liquid splashing from contaminating the clothes and hurting the skin. Protective gloves are also required, and chemical-resistant materials should be selected to avoid direct contact with the substance on the hands. Eye protection is also important. Protective glasses should be worn at any time to prevent accidental sputtering damage to the eyes.
Operating specifications should not be ignored. When weighing, measure accurately, and take according to the amount required for the experiment, not more or less. During the measurement process, the action should be stable to avoid the spilling of substances. During the reaction process, strictly control the temperature and control. Because of its reaction or sensitivity to temperature, there is a slight temperature difference, or the reaction results are very different. When heating, it is advisable to use suitable heating equipment and closely monitor the temperature change.
Caution is also required in post-reaction treatment. The remaining (2-bromo-5-iodophenyl) methanol should not be discarded at will. When in accordance with the regulations on chemical waste treatment, it should be collected by classification and properly disposed of to prevent pollution to the environment. The equipment used should be cleaned in time to remove the residual substances for next use.
In short, the safety and operation of (2-bromo-5-iodophenyl) methanol are related to the success or failure of the experiment, but also to the personal safety of the experimenter and the protection of the environment. Our chemical researchers should keep in mind and practice with caution.

Application Area

(2-Bromo-5-iodophenyl) methanol, this compound is used in the fields of medicine and chemical industry. In pharmaceutical research and development, because of its unique chemical structure, it can be used as a key intermediate to synthesize drugs with specific biological activities or to develop innovative therapies for specific diseases. In the chemical industry, it can participate in the synthesis of fine chemicals and contribute to the creation of new materials. Its bromine and iodine atoms give special reactivity, which can lead to various chemical reactions and help compound structure modification and function optimization. And this substance may emerge in the field of optical materials. With its structural properties, it may be able to develop materials with unique optical properties, which can be used in optical instruments, display technologies, etc. Due to its own characteristics, this compound has broad application prospects and potential value in many fields.

Research & Development

The recent study of (2-bromo-5-iodophenyl) methanol has been much considered. The method of its synthesis is quite critical. Looking for ancient books, there are also many lessons to be learned. Start with a certain method first, and after several transformations, it may be obtained. However, the details, such as the temperature, duration of the reaction, and the ratio of reagents, all need to be studied in detail.
Consider its application in the field of medicine, or it can be used as a key intermediate to synthesize special drugs. In terms of materials, it may also have unique properties and produce novel things.
In order to achieve progress, it is necessary to repeatedly test, observe its changes, and record its data. From the results of each time, summarize the advantages and disadvantages, and improve the method. Over time, I hope to make some achievements in the research and development of (2-bromo-5-iodophenyl) methanol, which will contribute to the academic community and promote progress in this field.

Toxicity Research

Since modern times, chemical refinement has produced all kinds of new substances. (2 - Bromo - 5 - Iodophenyl) Methanol This substance is also made of chemistry. However, we should investigate the fact and explore its toxicity, so as not to cause harm to the world.
The study of toxicity, the first look at its structure. The atoms of bromine and iodine in this substance may be potentially dangerous. Bromine, a genus of the halogen family, is sexually active. The same is true of iodine, and its effect on living organisms cannot be ignored.
The second study of its response to other substances. Under certain circumstances, (2 - Bromo - 5 - Iodophenyl) Methanol may react to produce new substances, and the toxicity of new substances is a different matter.
Furthermore, observe it experimentally. Take animals as models and observe their effects on this substance. Observe its physiological changes and different behaviors to show the toxicity.
In summary, the toxicity of (2 - Bromo - 5 - Iodophenyl) Methanol needs to be explored in many ways and treated with caution to ensure the well-being of the world and the environment is harmless.

Future Prospects

The (2-bromo-5-iodophenyl) methanol is also a new chemical material today. Its characteristics are specific, or it can be developed in the fields of organic synthesis and pharmaceutical research and development.
Looking at its future, it can be used in the creation of medicine, or as a key intermediate, to help the advent of new drugs and solve the suffering of the world. In organic synthesis, with its unique structure, it explores new synthesis paths and produces novel compounds.
Although at present, or due to cost and technology, it has not been widely used. However, over time, technology has advanced, costs have gradually declined, and technology has improved. We will spread our wings like Kunpeng, in the vast space of chemical industry and medicine, and do our best to become a bright pearl of future development, benefiting all living beings and flourishing the industry.

Where to Buy (2-Bromo-5-Iodophenyl)Methanol in China?

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Frequently Asked Questions

As a leading (2-Bromo-5-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.

(2-bromo-5-iodophenyl) What are the chemical properties of methanol?

(2-Bromo-5-iodophenyl) methanol, this is an organic compound. Its chemical properties are unique and closely related to the functional groups it contains.
Let's talk about the hydroxyl group first, which is active. First, a substitution reaction can occur. Take hydrohalic acid as an example, under suitable conditions, the hydroxyl group will be replaced by a halogen atom. Just like when reacting with hydrobromic acid, the hydroxyl group leaves, and the bromine atom joins to form the corresponding halogenated hydrocarbon. Second, the hydroxyl group can participate in the esterification reaction. When coexisting with carboxylic acid, in the environment of catalyst and heating, it will remove a molecule of water to form ester compounds. For example, when reacting with acetic acid, acetic acid (2-bromo-5-iodophenyl) methyl ester is formed. Third, the hydroxyl group can also be oxidized. If a weak oxidant, such as Sarit reagent, can be oxidized to an aldehyde group; if a strong oxidant is used, such as an acidic potassium permanganate solution, it will be further oxidized to a carboxyl group.
Looking at the halogen atom, the bromine atom is as active as the iodine atom. They can undergo nucleophilic substitution reactions. For example, in an alkaline environment, the halogen atom can be replaced by other nucleophilic reagents. Like co-heating with an aqueous solution of sodium hydroxide, the bromine atom or the iodine atom will be replaced by a hydroxyl group, but the reaction rate varies due to the different activities of bromine and iodine. In addition, halogen atoms can also participate in metal-organic reactions. For example, when reacted with magnesium, Grignard reagents can be formed. This Grignard reagent is widely used in organic synthesis and can react with many carbonyl compounds to grow carbon chains and synthesize organic compounds with diverse structures.
In summary, (2-bromo-5-iodophenyl) methanol is of great significance in the field of organic synthesis due to its active chemical properties of hydroxyl groups and halogen atoms. It can prepare organic compounds with complex structures through various reactions.

(2-bromo-5-iodophenyl) What is the synthesis method of methanol?

To prepare (2-bromo-5-iodophenyl) methanol, the method is as follows:
Take 2-bromo-5-iodobenzoic acid as the starting material. This compound reacts with lithium aluminum hydride in a suitable organic solvent, such as anhydrous tetrahydrofuran, at low temperature and under nitrogen protection. Lithium aluminum hydride is a strong reducing agent, and the carboxyl group (-COOH) can be reduced to hydroxymethyl (-CH -2 OH). After this reaction, (2-bromo-5-iodophenyl) methanol can be obtained. After the reaction is completed, the reaction mixture needs to be carefully handled. First, the excess lithium-aluminum hydride is carefully quenched with water, then neutralized with a dilute acid solution, and then the product is extracted with an organic solvent, such as dichloromethane. The extraction solution is dried by anhydrous sodium sulfate, and the solvent is evaporated to obtain a crude product. After column chromatography, a suitable eluent, such as a mixture of petroleum ether and ethyl acetate, is separated and purified to obtain pure (2-bromo-5-iodophenyl) methanol.
2-bromo-5-iodobenzaldehyde can also be used as a raw material. In a suitable solvent, such as methanol, sodium borohydride is added. This mild reducing agent can reduce the aldehyde group (-CHO) to hydroxymethyl. The reaction proceeded smoothly, and when the reaction was complete, the excess sodium borohydride was quenched with water, the methanol was evaporated under reduced pressure, diluted with water, and then extracted with an organic solvent. The subsequent drying, solvent evaporation and column chromatography purification steps were similar to the previous method, and the target product (2-bromo-5-iodophenyl) methanol could be obtained.

(2-bromo-5-iodophenyl) In what fields is methanol used?

(2-Bromo-5-iodophenyl) methanol, this compound has its uses in various fields. In the field of medicinal chemistry, it can be a key intermediate for the synthesis of specific drugs. The introduction of Gain bromide and iodine atoms endows the molecule with unique reactivity and spatial structure, which can precisely regulate the interaction between drugs and biological targets, thereby enhancing the efficacy of drugs and reducing side effects.
In the field of materials science, (2-bromo-5-iodophenyl) methanol may participate in the preparation of materials with special photoelectric properties. Its structural properties may enable it to play a role in organic Light Emitting Diodes (OLEDs), solar cells and other devices, helping to improve the charge transfer efficiency and optical properties of materials, and contributing to the research and development of new optoelectronic devices.
In the field of organic synthetic chemistry, this compound can be used as a multifunctional synthetic building block due to its bromine, iodine and alcohol hydroxyl functional groups. Through many organic reactions, such as nucleophilic substitution of halogenated hydrocarbons and oxidation of alcohols, complex and diverse organic molecules can be constructed, providing an important foundation for organic synthesis chemists to explore the structure and properties of novel compounds.

(2-bromo-5-iodophenyl) What are the physical properties of methanol?

(2-Bromo-5-iodophenyl) methanol, which is an organic compound. Looking at its physical properties, it is mostly solid under normal conditions. Its melting point can only be melted at a specific temperature due to intermolecular forces and structure. However, the exact value needs to be determined by fine experiments.
When it comes to solubility, because there are hydroxyl groups in the molecule, it has a certain polarity. It may have a certain solubility in polar solvents such as ethanol and methanol. Due to the principle of "similar miscibility", polar molecules are easily soluble in polar solvents. For non-polar solvents such as n-hexane, the solubility may be extremely low.
Its density is slightly higher than that of water in terms of atomic weight and molecular structure. And because it contains bromine, iodine and other atoms, the molecular weight increases, which also affects the density.
Furthermore, its appearance may be white to off-white powder or crystal, because most halogen-containing organic compounds and hydroxyl-containing compounds often have such appearance.
Its volatility, due to the presence of a certain force between molecules, is not very volatile, and requires specific conditions, such as heating, decompression, etc., to accelerate its volatilization rate.
To sum up, the physical properties of (2-bromo-5-iodophenyl) methanol are determined by its molecular structure and the atoms it contains. Under different scenarios, it exhibits different characteristics.

(2-bromo-5-iodophenyl) What is the market price of methanol?

I don't know the market price of (2-bromo-5-iodophenyl) methanol. The price of various substances in the market often changes due to many reasons, such as the abundance of materials, the difficulty of making, and the amount of demand.
If you want to know the exact market value of this product, you should consult the chemical material trading market, professional chemical suppliers, or find it on the online chemical product trading platform. Or refer to relevant chemical industry reports and information to clarify its approximate price. However, the price obtained through these channels is only a temporary reference and cannot be regarded as an eternal standard. Due to the ever-changing market, the price also moves. Therefore, if you want to get an accurate price, you must explore it in person and compare it with many parties to get it.