2 Bromo 5 Fluorobenzylamine
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Bromo-5-fluorobenzylamine
Chemical Formula C7H7BrFN
Molecular Weight 204.04
Appearance Solid (usually)
Solubility In Water Poorly soluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
Purity Typically high - >95% (in commercial products)
Chemical Formula C7H7BrFN
Molecular Weight 204.04
Appearance Typically a colorless to light - yellow liquid
Solubility Soluble in organic solvents like dichloromethane, chloroform, etc., poorly soluble in water
Purity Can be of various purities, e.g., 95%, 98% in commercial products
Hazard Class May be a skin and eye irritant, potential health hazard if ingested or inhaled
FAQ

What is the chemistry of 2-Bromo-5-fluorobenzylamine?

2-Bromo-5-fluorobenzyl amine is a class of organic compounds. It is active and has a wide range of uses in the field of organic synthesis.

In this compound, bromine and fluorine atoms have their own characteristics. Bromine atoms have large atomic radius and electronegativity, and can often be used as leaving groups in reactions to participate in nucleophilic substitution and other reactions. Due to the moderate bond energy of bromine-carbon bonds, when encountering nucleophilic reagents, easily broken bonds are replaced.

Fluorine atoms are famous for their extremely high electronegativity. After introducing molecules, they significantly affect the distribution of molecular electron clouds and enhance molecular polarity. This property not only affects the physical properties of compounds, such as boiling point, solubility, etc., but also changes the electron cloud density of ortho and para-sites in chemical reactivity, which affects the check point and activity of electrophilic substitution reactions.

Furthermore, the amino group of the benzylamine part has lone pairs of electrons, is basic, and can form salts with acids. It can also be used as a nucleophilic reagent to undergo nucleophilic substitution reactions with halogenated hydrocarbons, acyl halides, etc., to generate various nitrogen-containing derivatives. In organic synthesis, the reactivity of amino groups is often used to construct complex nitrogen-containing organic structures.

2-Bromo-5-fluorobenzamine exhibits unique chemical properties due to the synergistic effect of bromine, fluorine and benzylamine groups, providing organic synthesis chemists with diverse reaction pathways to create new functional materials, drug intermediates and many other organic compounds.

What are the main uses of 2-Bromo-5-fluorobenzylamine?

2-Bromo-5-fluorobenzyl amine is a commonly used raw material in organic synthesis. It has a wide range of uses and is often a key intermediate in the creation of new drugs in the field of medicinal chemistry. Due to the unique activity of halogen atoms and amino groups in the molecular structure, it can be cleverly combined with other compounds through many chemical reactions to build a complex molecular structure with specific physiological activities.

In terms of pesticide chemistry, 2-bromo-5-fluorobenzyl amine also plays an important role. Through a suitable synthesis path, it can be converted into pesticide ingredients with high insecticidal, bactericidal or herbicidal properties. Due to its structural properties, it can interact with specific biomacromolecules in pests, pathogens or weeds, interfering with their normal physiological and biochemical processes, thus achieving the effect of prevention and control.

Furthermore, in the field of materials science, 2-bromo-5-fluorobenzamine may participate in the preparation of functional materials. By polymerizing with other monomers or modifying the surface of existing materials, materials can be imparted with special optical, electrical or mechanical properties to meet the needs of different application scenarios.

In addition, at the level of scientific research and exploration, 2-bromo-5-fluorobenzylamine provides chemists with a variety of reaction possibilities, helping them to further explore the organic reaction mechanism, expand the organic synthesis methodology, and promote the continuous development of chemistry. In short, 2-bromo-5-fluorobenzylamine has shown significant value in many fields and is an indispensable and important compound in the field of organic chemistry.

What is 2-Bromo-5-fluorobenzylamine synthesis method?

To prepare 2-bromo-5-fluorobenzyl amine, you can follow the following method.

First take 2-bromo-5-fluorobenzoic acid as the starting material. It is heated with thionyl chloride. This step is to convert the carboxyl group into an acid chloride. Due to the reaction of thionyl chloride and carboxyl group, the corresponding acid chloride, sulfur dioxide and hydrogen chloride gas are generated. In this process, the acid chloride is prepared. After the reaction is completed, pure 2-bromo-5-fluorobenzoyl chloride can be obtained by distillation and other means.

The obtained 2-bromo-5-fluorobenzoyl chloride is slowly dripped into a reaction vessel containing excess concentrated ammonia water at low temperature. This step is an amidation reaction, the acid chloride interacts with ammonia to form 2-bromo-5-fluorobenzamide, and hydrogen chloride is generated at the same time. Excessive ammonia water can neutralize this hydrogen chloride. After the reaction is completed, 2-bromo-5-fluorobenzamide solid can be obtained after filtration, washing and other operations.

Finally, 2-bromo-5-fluorobenzamide is reacted with lithium aluminum hydride in an inert solvent such as anhydrous ethyl ether. Lithium aluminum hydride is a strong reducing agent, which can reduce the carbonyl group of the amide to methylene, thereby preparing 2-bromo-5-fluorobenzyl amine. After the reaction, a series of post-treatment operations such as hydrolysis (usually hydrolysis with dilute acid), extraction, drying and distillation can obtain a pure target product 2-bromo-5-fluorobenzyl amine.

Or it can be started from 2-bromo-5-fluorobenzyl bromide. 2-Bromo-5-fluorobenzyl bromide is reacted with sodium cyanide in a suitable solvent (e.g. N, N-dimethylformamide) to form 2-bromo-5-fluorobenzylacetonitrile. This is a nucleophilic substitution reaction in which cyanogen ions replace bromine ions. After that, 2-bromo-5-fluorobenzylacetonitrile is reduced with a suitable reducing agent (e.g. hydrogenation catalyzed by Raney nickel, or lithium aluminum hydride, etc.), and 2-bromo-5-fluorobenzylamine can also be obtained. After the reaction is completed, appropriate subsequent treatment steps are also required to obtain a purified product.

2-Bromo-5-fluorobenzylamine What are the precautions in storage and transportation?

2-Bromo-5-fluorobenzyl amine is one of the organic chemicals. When storing and transporting, you need to be cautious.

First talk about storage. This material is active and easy to react with surrounding objects, so it must be placed in a cool, dry and well-ventilated place. If it is in a high temperature and humid place, it may cause deterioration and damage its chemistry and purity. Cover high temperature can promote its decomposition, and moisture can lead to hydrolysis and other reactions. And it should be kept away from fire and heat sources. Because it is flammable, it is easy to cause fire in case of open fire or hot topic. At the same time, it should be stored in isolation from oxidants, acids, etc. The edge oxidant has strong oxidizing properties, and the acid is chemically active. It can react violently with 2-bromo-5-fluorobenzyl amine, causing danger.

As for transportation, it should not be ignored. It is necessary to ensure that the packaging is intact to prevent leakage. The packaging material must be resistant to corrosion of this substance, strong and well sealed. During transportation, the traffic should be stable to avoid severe vibration and impact. Otherwise, the packaging will be damaged and 2-bromo-5-fluorobenzyl amine will leak, which will not only pollute the environment, but also pose a hazard to the transportation personnel. In addition, the transportation vehicle should be equipped with corresponding fire equipment and leakage emergency treatment equipment. In case of an emergency, it can be responded to in time. The escort personnel should also be familiar with the characteristics of this substance and the emergency response method, and always pay attention to the transportation situation to ensure the safety of the whole process.

What is the market price of 2-Bromo-5-fluorobenzylamine?

In today's world, business conditions are fickle, and the price of 2-Bromo-5-fluorobenzylamine in the market is difficult to determine. Its price often changes for many reasons, such as the source of materials, the method of production, the amount of demand, and the rise and fall of the market.

The source of materials, if the raw materials it relies on are abundant, the price may tend to be flat; if the raw materials are scarce, it is not easy to find, and the price will rise. If the production method has new skills, it can increase production and reduce consumption, and the price may drop; if the process is difficult, the cost will be high, and the price will also rise.

Furthermore, the amount of demand is related to the market price. If there are many people in various industries who need this product, the supply is in short supply, and the price is self-rising; if there are few people who want it, the supply is in excess of demand, and the price is likely to drop. And the rise and fall of the market is also the key. When the market is prosperous, all industries are prosperous, and transactions are frequent, the price may rise steadily; if the market is depressed, the economy is sluggish, and transactions are sluggish, the price may not be firm.

To know the exact market value of this product, when the market of chemical materials is scrutinized carefully, or the merchants who specialize in it, or visit the platform of chemical trading, the prices of all companies can be reviewed, and the general price can be obtained. However, it is only a temporary situation and cannot be relied on for a long time.