4 Bromo 2 Fluorobenzylamine Hydrochloride
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
4-Bromo-2-fluorobenzylamine hydrochloride
Chemical Formula C7H8BrClFN
Molecular Weight 226.5
Appearance Typically a white to off - white solid
Melting Point N/A (data may vary, check specific literature)
Boiling Point N/A (data may vary, check specific literature)
Solubility In Water Moderate to high solubility, being a hydrochloride salt
Solubility In Organic Solvents Soluble in some polar organic solvents like methanol, ethanol
Density N/A (data may vary, check specific literature)
Purity Typically sold in high purity grades, e.g., 95%+
Storage Conditions Stored in a cool, dry place, protected from light
Chemical Formula C7H8BrClFN
Molecular Weight 226.5
Appearance Solid
Color White to off - white
Solubility In Water Soluble
Melting Point 185 - 189 °C
Purity Typically high purity (e.g., 95%+)
FAQ

What are the chemical properties of 4-Bromo-2-fluorobenzylamine hydrochloride?

4-Bromo-2-fluorobenzyl amine hydrochloride is a genus of organic compounds. It is active and has a variety of chemical characteristics.

Looking at its physical properties, it is mostly white to quasi-white crystalline powder at room temperature, which is due to the intermolecular forces and arrangement. In water, it has a certain solubility, which is due to its amino hydrochloride structure, which can form hydrogen bonds with water molecules to help it disperse. In organic solvents such as ethanol and acetone, the solubility is also good. Due to the principle of similar miscibility, its organic structure is compatible with organic solvent molecules.

When it comes to chemical properties, the part of amino hydrochloride is acidic. In case of a base, the hydrogen ion of hydrochloride will react with the hydroxide ion in the base to form water, which in turn prompts the free amine group. This free amine group has nucleophilic properties and can react with many electrophilic reagents. For example, when it encounters an acyl chloride, the amine nitrogen atom will launch a nucleophilic attack on the carbonyl carbon of the acyl chloride, and through a series of changes, amide compounds will be formed. This reaction is often used in organic synthesis to construct structures containing amide bonds, laying the foundation for the preparation of drugs and materials.

Furthermore, the carbon-bromine bond at the benzyl position is relatively active. Under suitable conditions, nucleophilic substitution reactions can occur. Like when coexisting with nucleophiles in an alkaline environment, nucleophiles will attack the carbon atoms connected to bromine, and bromine ions leave to realize the substitution process. This property can be used to introduce different functional groups to expand the diversity of compound structures. Although fluorine atoms on the benzene ring are relatively stable, they can also participate in the reaction under specific strong conditions, affecting the reactivity and selectivity of the molecule as a whole.

4-Bromo-2-fluorobenzyl amine hydrochloride is widely used in the field of organic synthesis due to its unique chemical properties. It provides key raw materials and reaction intermediates for the creation of novel compounds, the exploration of new materials and the development of drugs.

What are the uses of 4-Bromo-2-fluorobenzylamine hydrochloride?

4-Bromo-2-fluorobenzyl amine hydrochloride has a wide range of uses in the field of medicinal chemistry. First, it is often a key intermediate in the process of drug development. Due to its unique chemical structure, it can introduce specific functional groups through various chemical reactions, thereby constructing compounds with specific biological activities, or as potential therapeutic drugs. For example, nucleophilic substitution reactions can be used to combine with reagents containing specific groups to create new drug molecular architectures to explore their effects on specific disease targets.

Second, in the field of materials science, it may also have its own uses. Its active groups can be used to participate in the modification reactions on the surface of materials. By grafting 4-bromo-2-fluorobenzyl amine hydrochloride on the surface of the material, the material is endowed with unique chemical properties, such as improving the hydrophobicity of the material, enhancing the interaction between the material and biomolecules, etc., which have potential application value in biomedical materials, sensor materials, etc.

Furthermore, in the field of organic synthetic chemistry, it is favored by organic synthetic chemists. Due to its particularity of structure, it can be used as a starting material to construct complex organic molecular systems through multi-step reactions. It can expand the carbon chain by reacting with different organic reagents, such as alkenes, alkynes, etc., and then enrich the structural diversity of organic compounds, providing a basis for the discovery of new organic functional materials and drug lead compounds.

What is the synthesis method of 4-Bromo-2-fluorobenzylamine hydrochloride?

The synthesis of 4-bromo-2-fluorobenzyl amine hydrochloride is a key issue in the field of organic synthesis. The synthesis method is often based on existing chemical principles and the experience accumulated by predecessors.

First, the choice of raw materials is very important. 4-bromo-2-fluorobenzoic acid is often used as the starting material because the raw material contains the key structural fragments required by the target product. Starting from 4-bromo-2-fluorobenzoic acid, to obtain 4-bromo-2-fluorobenzyl amine hydrochloride requires multiple steps of conversion.

First, 4-bromo-2-fluorobenzoic acid can be converted into the corresponding acid chloride first. This step is usually reacted with thionyl chloride and other reagents, and heating prompts the reaction to occur, resulting in 4-bromo-2-fluorobenzoyl chloride. The reason for this reaction is that the active chlorine atom of thionyl chloride can replace the hydroxyl group of benzoic acid to form an acid chloride structure.

Then, 4-bromo-2-fluorobenzoyl chloride reacts with ammonia to obtain 4-bromo-2-fluorobenzoamide. The reaction conditions in this step are relatively mild, and ammonia can undergo nucleophilic substitution with the carbonyl group of the acid chloride to form an amide.

Then 4-bromo-2-fluorobenzamide is treated with a strong reducing agent such as lithium aluminum hydride, and the carbonyl group of the amide is reduced to methylene to obtain 4-bromo-2-fluorobenzyl amine. The hydrogen anion of lithium aluminum hydride undergoes nucleophilic attack on the amide carbonyl carbon, and the reduction of the carbonyl group is achieved through a series of transformations.

Finally, 4-bromo-2-fluorobenzyl amine is reacted with hydrogen chloride gas or hydrochloric acid solution to obtain the target product 4-bromo-2-fluorobenzyl amine hydrochloride. This step is an acid-base neutralization reaction, where the amine group binds hydrogen ions to form an ammonium salt to obtain the hydrochloride form.

During the synthesis process, it is necessary to pay attention to the reaction conditions of each step, such as temperature, reaction time, reagent dosage, etc., which have a significant impact on the yield and purity of the product. And after each step of the reaction, it is often necessary to separate and purify methods, such as extraction, distillation, column chromatography, etc., to remove impurities and ensure that the reaction proceeds in the expected direction, and finally 4-bromo-2-fluorobenzyl amine hydrochloride is efficiently obtained.

What is the market price of 4-Bromo-2-fluorobenzylamine hydrochloride?

The market price of 4-bromo-2-fluorobenzyl amine hydrochloride is difficult to determine. The price is influenced by various factors, such as raw material cost, simple preparation process, market supply and demand, and manufacturers and trading seasons.

In the past, the cost of raw materials was the key to the price. If the price of bromide, fluoride and other raw materials required for the synthesis of this compound is too expensive, or due to changes in origin and shortage of resources, the price of this compound will also rise. If the preparation process is complicated, it requires multiple steps of reaction, special catalysts or harsh reaction conditions, consumes manpower and material resources, and will also make its price not low.

Market supply and demand are also the main reasons. If many pharmaceutical companies and scientific research institutions have strong demand for this compound, and the demand is greater than the supply, the price will be high; conversely, if the demand is weak and the supply is abundant, the price will tend to decline.

Different manufacturers have different pricing due to different technical levels and economies of scale. Large scale and superior technology, the cost is controllable, and the price is close to the people; small factories have high costs, and the price may be high.

Seasonal factors cannot be ignored. During a specific period, such as the harvest season of raw materials, the cost will drop, and the price may be low; while when the supply of raw materials is tight, the price will rise.

Therefore, in order to know the exact market price, when consulting the relevant chemical product suppliers, trading platforms, or in the chemical market survey, we can get the price that fits the current market.

4-Bromo-2-fluorobenzylamine hydrochloride in storage and transportation

4-Bromo-2-fluorobenzyl amine hydrochloride is a chemical substance, and many things must be carefully paid attention to during storage and transportation.

First, when storing, it should be placed in a cool, dry and well-ventilated place. Because it is quite sensitive to humidity, the humid environment can easily cause deterioration, so the humidity in the warehouse must be properly controlled. And the temperature should not be too high, high temperature may cause chemical reactions and endanger the stability of the substance.

Second, this chemical is toxic and corrosive. When storing, it must be stored separately from oxidants, acids, bases, etc., and must not be mixed to prevent violent reactions or even safety accidents. At the same time, the storage area should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment for emergencies.

Third, during transportation, the relevant regulations must be strictly followed. The packaging must be solid to ensure that it will not be damaged or leaked during transportation. The transportation vehicle should also have good ventilation conditions to avoid excessive temperature and humidity in the compartment. The escort personnel must be familiar with the characteristics of the chemical substance and emergency treatment methods, and regularly check whether the packaging is in good condition during transportation.

Fourth, whether it is storage or transportation, it is necessary to make a good mark. Clearly mark the warning words "toxic" and "corrosive", so that the contact person can see at a glance and be vigilant, so as to avoid safety problems caused by accidental touch and misuse. In this way, 4-bromo-2-fluorobenzyl amine hydrochloride can be properly stored and transported to ensure personnel safety and material stability.