2 Azidomethyl 1 3 Difluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-(azidomethyl)-1,3-difluorobenzene
Chemical Formula C7H5F2N3
Molecular Weight 169.13 g/mol
Chemical Formula C7H4F2N3
Molecular Weight 169.12 g/mol
Physical State At Room Temperature Likely liquid (educated guess from similar azide - containing aromatic compounds)
Solubility Soluble in organic solvents like dichloromethane, chloroform (common for aromatic halide - azide compounds)
Hazard Class Azides are often explosive and toxic, so likely a high - hazard class due to azide group
Chemical Formula C8H5F2N3
Molar Mass 181.14 g/mol
Appearance likely a colorless to pale - colored liquid or solid
Solubility In Water likely low, as it is an organic compound with non - polar benzene ring and azide group
Solubility In Organic Solvents soluble in common organic solvents like dichloromethane, chloroform, etc. due to its organic nature
Hazard Class azide - containing compound, potentially explosive, and azides can be toxic
Chemical Formula C7H5F2N3
Molecular Weight 169.13
Appearance Typically a liquid or solid (physical state depends on conditions)
Boiling Point Data may vary depending on purity and pressure
Melting Point Data may vary depending on purity
Density Data may vary depending on conditions
Solubility Solubility characteristics would depend on the solvent, may be sparingly soluble in water, more soluble in organic solvents
Vapor Pressure Data may vary depending on temperature
Flash Point Data may vary depending on purity and testing method
Hazard Class May be classified as a hazardous substance due to azide group (risk of explosion, toxicity concerns)
FAQ

What is the main use of 2- (azidomethyl) -1,3-difluorobenzene?

2-%28azidomethyl%29-1%2C3-difluorobenzene is 2 - (azidomethyl) -1,3 -difluorobenzene, which is very important in the field of organic synthesis.

First, it plays a significant role in the construction of nitrogen-containing heterocyclic compounds. Azido groups are active and can be converted through various reactions, such as cycloaddition reaction with alkynes, known as click chemistry, which can efficiently generate triazole heterocycles. This reaction has mild conditions and good selectivity, and is widely used in the fields of medicinal chemistry and materials science. Triazole structures are commonly found in many bioactive molecules, such as antibacterial and antiviral drugs. By means of this reaction, such structures can be easily introduced, providing a powerful way for the development of new drugs.

Second, it also has important uses in material modification. Because of its azido group, it can react with polymers containing alkynyl groups or other groups that can react with it, thereby introducing the difluorobenzene structure into the main chain or side chain of the polymer. The introduction of fluorine atoms can change the surface properties of the material, such as enhancing hydrophobicity and chemical stability; at the same time, azido groups participate in the reaction to achieve material crosslinking, improve the mechanical properties and thermal stability of the material, and have broad application prospects in the preparation of high-performance polymer materials.

Third, 2 - (azidomethyl) -1,3 - difluorobenzene can be used as a key intermediate to participate in the total synthesis of complex organic molecules. Its unique structure can provide a variety of possibilities for subsequent reactions. By rationally designing the reaction route, complex carbon skeletons and functional group systems can be gradually constructed, playing an important role in the frontier fields of organic synthesis such as total synthesis of natural products, and assisting chemists in exploring new organic compounds with structures and functions.

What are the physical properties of 2- (azidomethyl) -1,3-difluorobenzene

2 - (azomethyl) -1,3 -difluorobenzene is one of the organic compounds. Its physical properties are quite important and may have applications in various fields of chemical industry.

Looking at its physical state, it is mostly liquid at room temperature and pressure. This is due to the intermolecular force, which causes its melting and boiling point to be in a specific range. Its melting point may be lower due to the regularity and interaction of molecular structures, and the boiling point is determined by the molecular mass and the strength of the intermolecular force. Generally speaking, the boiling point is neither too high nor too low, which makes it easy to control under specific reaction conditions.

Furthermore, its solubility is also characteristic. In organic solvents, such as ethanol, ether, etc., or have good solubility. Due to the principle of similar miscibility, the molecular structure of the compound and the molecules of the organic solvent may form appropriate forces, such as van der Waals force, etc., so it can dissolve in it. However, in water, its solubility may not be good, because the polarity of its molecules does not match the polarity of water molecules, and there is a lack of groups that form strong interactions with water molecules, such as water-soluble groups.

Its density is also an important physical property. Compared with water, its density may be different, which needs to be paid attention to in separation, extraction and other operations. If the density is greater than water, in the relevant liquid-liquid system, it may sink in the lower layer; if it is less than water, it may float in the upper layer.

In addition, its volatility also needs to be considered. Due to the degree of intermolecular forces, it may be volatile at a certain temperature. This property should be taken into account during storage and use, and should be stored in a suitable environment to prevent volatilization from causing losses or causing safety problems.

What is the chemical synthesis method of 2- (azidomethyl) -1,3-difluorobenzene?

To prepare 2 - (azomethyl) -1,3 - difluorobenzene, you can do it as follows.

Take 1, 3 - difluorobenzene first, and make it chloromethylated with polyformaldehyde and hydrochloric acid under the action of suitable catalysts. This reaction needs to be controlled at a certain temperature and pay attention to the proportion of materials. 2 - (chloromethyl) -1,3 - difluorobenzene can be obtained.

Then, 2 - (chloromethyl) -1,3 - difluorobenzene is reacted with sodium azide in a suitable solvent. This solvent should be selected with good solubility to the reactants and does not react violently with sodium azide, such as N, N-dimethylformamide (DMF). During the reaction, it is necessary to pay attention to the reaction process, because the azide has certain risks, it is necessary to operate with caution. After this reaction, 2 - (azomethyl) -1,3 - difluorobenzene can be obtained.

There are other ways. If 1,3 - difluorobenzoic acid is used as the starting material, 1,3 - difluorobenzyl alcohol is first obtained by reduction reaction, and then it is reacted with p-toluenesulfonyl chloride to obtain 1,3 - difluorobenzyl sulfonate. After reacting with sodium azide, the target product 2- (azidomethyl) -1,3-difluorobenzene can also be obtained.

During the preparation process, each reaction step needs to be strictly controlled and controlled, and the product needs to be carefully separated and purified to ensure the purity and yield of the product. And because azide is involved, safety procedures must be followed to prevent accidents.

2- (azidomethyl) -1,3-difluorobenzene What are the precautions during storage and transportation?

2-%28azidomethyl%29-1%2C3-difluorobenzene is 2- (azidomethyl) -1,3-difluorobenzene. When storing and transporting this substance, pay attention to many matters.

It has azido groups, is chemically active, and has poor stability. When storing, it must be placed in a cool, dry and well-ventilated place. Keep away from fire and heat sources. It is easy to cause decomposition due to heat, and even trigger explosion, which is very dangerous. And it should be stored separately from oxidizing agents, acids, and alkalis to prevent dangerous interactions. Because it is sensitive to vibration and friction, the storage place should avoid strong vibration and impact.

During transportation, be sure to pack tightly and firmly to ensure that there is no risk of leakage. Select a transportation tool specially suitable for such dangerous chemicals, and the transportation personnel need to be professionally trained to be familiar with its characteristics and emergency treatment methods. During transportation, always monitor environmental factors such as temperature and vibration, keep a smooth ride, and avoid violent actions such as sudden braking and sharp turns. If a leak occurs during transportation, personnel should quickly evacuate to a safe area and deal with it strictly according to the emergency plan to prevent the accident from expanding. In short, the storage and transportation of 2- (azomethyl) -1,3-difluorobenzene must be treated with caution and follow relevant regulations and operating procedures to ensure safety.

What are the effects of 2- (azidomethyl) -1,3-difluorobenzene on the environment and human health?

2-%28azidomethyl%29-1%2C3-difluorobenzene, that is, 2 - (azidomethyl) -1,3 -difluorobenzene, the impact of this substance on the environment and human health needs to be examined in detail.

At the environmental level, if it is released into nature, it may have complex effects. Because of its special chemical structure, azido groups and fluorine atoms make it unique in chemical properties. If it flows into the water body, it may be difficult to degrade rapidly, because of the stability of azido groups, it can be retained for a long time. If aquatic organisms come into contact, it may cause many negative effects. Azido groups may interfere with biochemical reactions in organisms, and fluorine atoms can affect the structure and function of biofilms. It may cause aquatic organisms to inhibit growth, reduce reproduction, and even die. In the soil environment, it may be adsorbed on soil particles, affecting the structure and function of soil microbial community. Microorganisms participate in soil material circulation and nutrient transformation, and they are disturbed or cause soil ecosystem imbalance and affect vegetation growth.

As for human health, 2 - (azidomethyl) -1,3 - difluorobenzene also has latent risk. Inhalation through the respiratory tract can irritate the respiratory mucosa, causing symptoms such as cough, asthma, and breathing difficulties. Long-term exposure may damage lung function and increase the risk of respiratory diseases. If exposed through the skin, it may be fat-soluble or penetrate the skin barrier into the human body. Or cause skin allergic reactions, causing redness, swelling, itching, rashes, etc. And after entering the human body, it can circulate to various organs and tissues through the blood, interfering with normal physiological functions. Azido groups may react with biological macromolecules such as proteins and nucleic acids, destroying their structure and function, increasing the risk of genetic mutation and carcinogenesis.

Therefore, for 2 - (azidomethyl) -1,3 - difluorobenzene, it needs to be treated with caution, and its production, use and emission should be strictly controlled to reduce its potential harm to the environment and human health.