2 Bromo 4 Aminomethyl Thiazole
quinoline thiophene imidazole thiazole

2-Bromo-4-(aminomethyl)thiazole

    Specifications

    HS Code

    894247

    Chemical Formula C4H5BrN2S
    Molecular Weight 193.064 g/mol
    Appearance Solid (likely, based on similar compounds)

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    General Information
    Where to Buy 2-Bromo-4-(aminomethyl)thiazole in China?
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    Frequently Asked Questions

    As a leading 2-Bromo-4-(aminomethyl)thiazole supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main uses of 2-Bromo-4- (aminomethyl) thiazole?
    2-Bromo-4- (aminomethyl) thiazole is widely used in the fields of medicine and chemical industry.
    In the way of pharmaceutical research and development, it can be a key traditional Chinese medicine for creating novel antibacterial and anti-inflammatory agents. Due to the unique chemical structure and biological activity of the thiazole ring, the introduction of bromine atoms and aminomethyl can precisely regulate the electron cloud distribution and spatial configuration of molecules, enhance the interaction between agents and targets, and enhance the antibacterial and anti-inflammatory effects.
    In the process of chemical production, it can be used as a raw material for the synthesis of special materials. With its reactive groups, complex polymer structures can be constructed through many chemical reactions, such as nucleophilic substitution, condensation, etc., endowing materials with special properties such as high stability and unique optical properties. It has great potential in optoelectronic materials, high-performance polymers and other fields.
    Furthermore, it is also an important intermediate in the field of organic synthetic chemistry. Through its participation in various reactions, it can derive a wide range of organic compounds with rich structures, contributing to the development of organic synthetic chemistry and helping scientists create more new functional molecules to meet the needs of different fields.
    What are the synthesis methods of 2-Bromo-4- (aminomethyl) thiazole
    To prepare 2-bromo-4- (aminomethyl) thiazole, the method is as follows:
    First, take a suitable starting material, often thiazole compounds as the base. If 4-methylthiazole is used as the starting point, and aminomethyl is introduced to it at the 4-position, 4-methyl can be converted to 4-halomethyl by halogenation reaction. If a brominating agent, such as N-bromosuccinimide (NBS), is used in the presence of an initiator such as benzoyl peroxide, light or heat, 4-methylthiazole undergoes a free radical substitution reaction to obtain 4-bromomethylthiazole. This step requires controlling the reaction conditions, such as temperature, proportion of reactants, and reaction time, to prevent side reactions of polyhalogenation.
    Then, 4-bromomethyl thiazole is converted to 4- (aminomethyl) thiazole. It can react with ammonia sources, either liquid ammonia or ammonia water. In a suitable reaction vessel, control the temperature and maintain a certain pressure (when liquid ammonia is used as the ammonia source), and react for a period of time to replace the bromomethyl with ammonia to generate 4- (aminomethyl) thiazole.
    Finally, 4 - (aminomethyl) thiazole is brominated at the 2-position. A brominating reagent, such as bromine (Br ²), can be selected. In an appropriate solvent such as dichloromethane, bromine is slowly added dropwise at low temperature with a suitable catalyst such as iron powder to carry out an electrophilic substitution reaction to obtain the target product 2-bromo-4- (aminomethyl) thiazole. After the reaction is completed, the pure product is obtained by separation and purification, such as extraction, column chromatography, etc. The whole synthesis process needs to follow the reaction characteristics of each step and precisely control the conditions to obtain a product with good yield and purity.
    What are the physicochemical properties of 2-Bromo-4- (aminomethyl) thiazole?
    2-Bromo-4- (aminomethyl) thiazole is one of the organic compounds. Its physical and chemical properties are of paramount importance and are related to many properties and applications of this compound.
    In terms of its physical properties, under normal temperature and pressure, or as a solid state, looking at its color, it is often white to light yellow powder or crystalline. This is because its molecular structure is arranged in an orderly manner, resulting in the formation of a specific aggregate state. Its melting point is also one of the key physical properties. It has been experimentally determined to be around [specific melting point value]. The existence of this melting point causes the compound to undergo a phase transition under specific temperature conditions. In addition, its solubility is also worth exploring. It has a certain solubility in common organic solvents, such as ethanol and dichloromethane. Due to the interaction force between molecules and solvent molecules, it can be uniformly dispersed in the solvent system.
    As for the chemical properties, the bromine atoms in this compound are extremely active. Bromine atoms have strong electronegativity, which makes them prone to substitution reactions. When encountering nucleophiles, bromine atoms can be replaced by nucleophilic groups, thereby forming new carbon-heteroatomic bonds. The aminomethyl part, because its amino group has lone pairs of electrons, is basic and can neutralize with acids to form corresponding salts. At the same time, the thiazole ring also endows the compound with unique chemical stability and reactivity. The conjugated structure of the thiazole ring reduces the molecular energy and enhances the stability; however, the uneven distribution of electron clouds on the ring provides an active checking point for chemical reactions.
    The physicochemical properties of this compound lay the foundation for its application in organic synthesis, drug development and other fields. Many chemists and researchers have studied it in depth because of its unique properties, hoping to explore more potential uses.
    What is the price range of 2-Bromo-4- (aminomethyl) thiazole in the market?
    I don't know the price range of 2 - Bromo - 4 - (aminomethyl) thiazole in the market. This is not a common traditional thing that I know of, and there is no past experience to find its price. Although "Tiangong Kaiwu" is a strange book, it does not contain the price of such novel chemicals. In today's world, the price of chemical substances often changes for many reasons, such as the abundance of raw materials, the difficulty of making methods, the amount of demand, the distance of the region, and the rise and fall of market conditions. If you want to know the exact price, or ask a merchant specializing in chemical materials, or look for market information and professional quotation platforms for chemical product trading, you can get a more accurate price range.
    What are the safety and precautions of 2-Bromo-4- (aminomethyl) thiazole
    2-Bromo-4- (aminomethyl) thiazole is a chemical substance. Regarding its safety and precautions, it is hereby stated as follows.
    This substance has potential chemical activity or poses certain hazards. In terms of safety, it may have adverse effects on human health. Contact with it or irritate the skin, causing redness, itching, pain and other discomfort. If not accidentally entered the eyes, it can cause severe eye pain, redness, swelling, tears, and even damage vision. Inhalation of its volatile gaseous substances, or irritation of the respiratory tract, causing cough, asthma, breathing difficulties and other symptoms. Long-term or large-scale exposure, or affect the normal function of internal organs of the human body, such as liver, kidneys, etc., or there is a potential risk of carcinogenesis and teratogenesis. However, more research is needed to confirm the exact extent.
    As for precautions, when handling this substance, it is necessary to strictly abide by safety procedures. Operators should wear protective clothing, such as laboratory clothes, protective aprons, etc., to prevent direct contact with the skin. Protective gloves must be worn. The material should be chemically resistant, such as nitrile gloves. Take them off in time after operation and wash your hands. Eye protection is also indispensable. Goggles should be worn to prevent substances from splashing in. The operating environment should be well ventilated and preferably carried out in a fume hood to quickly discharge volatile gaseous substances and reduce the concentration in the air.
    In case of inadvertent contact, the treatment method should also be clear. For skin contact, rinse quickly with a large amount of flowing water, at least 15 minutes, and then seek medical attention as appropriate. For eye contact, immediately open the eyelids, rinse with a large amount of water, continue for more than 15 minutes, and seek medical attention quickly. Those who inhale, quickly move to a fresh air place to keep the respiratory tract unobstructed. If breathing difficulties, give oxygen and send it to the hospital as soon as possible.
    In addition, the storage of this substance should also be paid attention to. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources, to prevent its chemical properties from changing due to temperature and humidity discomfort, which may cause danger. And it should be stored separately from oxidants, acids, bases and other substances to avoid chemical reactions caused by mixed storage.
    In short, the operation of 2-bromo-4- (aminomethyl) thiazole requires caution at all times and strict adherence to safety regulations to prevent accidents and ensure personal safety and environmental safety.