3 Amino 2 Bromo 6 Trifluoromethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

3-Amino-2-bromo-6-(trifluoromethyl)pyridine

    Specifications

    HS Code

    401836

    Chemical Formula C6H4BrF3N2
    Molecular Weight 241.01
    Appearance Solid (likely)
    Solubility In Water Low solubility (expected due to non - polar groups)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (expected)
    Reactivity Reactive towards nucleophiles due to the bromine atom

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    General Information
    Where to Buy 3-Amino-2-bromo-6-(trifluoromethyl)pyridine in China?
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    Frequently Asked Questions

    As a leading 3-Amino-2-bromo-6-(trifluoromethyl)pyridine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the main use of 3-Amino-2-bromo-6- (trifluoromethyl) pyridine?
    3-Amino-2-bromo-6- (trifluoromethyl) pyridine is a crucial compound in the field of organic synthesis. It has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry to assist in the synthesis of many biologically active drug molecules. Due to the structure of the pyridine ring and the specific substituents attached to it, the compound has unique chemical properties and is suitable for constructing complex drug molecular structures. For example, it can be coupled with other compounds containing specific functional groups through a series of organic reactions to generate new substances with specific pharmacological activities, which is of great significance for the development of antibacterial, antiviral and anti-tumor drugs.
    In the field of materials science, 3-amino-2-bromo-6- (trifluoromethyl) pyridine also plays an important role. Due to the presence of fluorine atoms, the material has unique electrical, optical and thermal properties. It can be used to prepare organic optoelectronic materials, such as organic Light Emitting Diodes (OLEDs), organic solar cells, etc., to improve the charge transport performance and stability of materials, and then optimize device performance.
    In addition, this compound also has potential application value in the field of pesticide chemistry. Its structural characteristics may give it a certain biological activity, which can be used as a lead compound for structural modification and optimization, and new pesticides with high efficiency, low toxicity and environmental friendliness can be developed for crop pest control and agricultural production.
    What are the synthesis methods of 3-Amino-2-bromo-6- (trifluoromethyl) pyridine
    The synthesis method of 3-amino-2-bromo-6- (trifluoromethyl) pyridine has been used throughout the ages, and various methods have their own wonders. One of the common methods starts with the corresponding pyridine derivative. First take the pyridine compound containing a specific substituent, use halogenation, select suitable halogenated reagents, such as bromine or bromine-containing compounds, and introduce bromine atoms into the designated position under appropriate reaction conditions to obtain bromine-containing pyridine intermediates. This process requires careful regulation of temperature, reaction time and reagent dosage to achieve the best reaction effect.
    Then, modify by amination. Select a suitable amination reagent or amine compound in a specific reaction system to react with the above bromine-containing intermediates. The reaction environment such as the choice of solvent and the control of pH are all crucial. Or the power of the catalyst can be used to accelerate the reaction process and improve the yield of the product.
    Another way is to start with the construction of the pyridine ring. Select the raw materials containing fluorine, bromine and amino latent functional groups, and use the cyclization reaction to build the pyridine skeleton. The reaction mechanism is intricate, and the reaction route needs to be carefully designed to consider the compatibility of the reaction conditions at each step. Or through a multi-step reaction, each substituent is gradually introduced, and each step of transformation is finely regulated, so that each functional group is in place in sequence, and the final product is 3-amino-2-bromo-6- (trifluoromethyl) pyridine.
    The synthesis method is ever-changing, relying on the ingenuity and practice of chemists, and finding a balance between various reaction conditions to achieve the purpose of efficient and high-purity synthesis.
    What are the physical properties of 3-Amino-2-bromo-6- (trifluoromethyl) pyridine
    3-Amino-2-bromo-6- (trifluoromethyl) pyridine is an organic compound with unique physical properties.
    It is a solid at room temperature and pressure. Due to the presence of halogen atoms such as bromine and fluorine in the molecular structure, the intermolecular force is enhanced, and the melting boiling point is relatively high. Generally speaking, the melting point is in a specific temperature range, but the exact value varies depending on the purity and test conditions.
    The appearance of this compound is often white to off-white crystalline powder with fine texture. Its solubility is also an important physical property. It has a certain solubility in organic solvents such as dichloromethane, chloroform, N, N-dimethylformamide (DMF), etc., because these organic solvents can form interactions such as van der Waals forces and hydrogen bonds with the compound, which can help it disperse and dissolve. The solubility in water is low, because the hydrophobic trifluoromethyl in the molecule accounts for a large proportion, which reduces the ability to form hydrogen bonds with water molecules and makes it hydrophilic.
    In terms of density, due to the large relative atomic mass of bromine atoms and trifluoromethyl, the density of this compound is higher than that of common hydrocarbon compounds, but the specific density value is also affected by factors such as temperature and pressure. < Br >
    Its stability is acceptable under appropriate conditions, but due to the presence of active amino groups and bromine atoms, chemical reactions may occur under extreme conditions such as strong acids, strong bases, strong oxidants or high temperatures, resulting in structural changes.
    The physical properties of 3-amino-2-bromo-6 - (trifluoromethyl) pyridine are determined by its molecular structure. These properties are of great significance for its separation, purification, and choice of reaction conditions in the fields of organic synthesis, pharmaceutical chemistry, etc.
    What is the price range of 3-Amino-2-bromo-6- (trifluoromethyl) pyridine in the market?
    I don't know what the price range of 3-amino-2-bromo-6- (trifluoromethyl) pyridine is in the market. However, there are many ways to know the price of this product. First, you can consult chemical raw material suppliers. They often sell various chemicals, or can know the price of this product. On the chemical product trading platform, you can also get relevant quotations. The platform gathers a wide range of merchants, and the price information is quite rich.
    Furthermore, in academic journals and research reports, or related to the preparation cost of this product, although it is not a direct price, it can also slightly push the price range according to the cost. If you look for professional chemical information institutions, they specialize in market analysis and are quite familiar with the price dynamics of various chemicals, and can provide more accurate price information.
    However, market prices often change from time to time, and raw material costs, supply and demand, and preparation processes can all fluctuate. To know the exact price, multiple parties must inquire, and real-time information shall prevail.
    What are the relevant safety precautions for 3-Amino-2-bromo-6- (trifluoromethyl) pyridine?
    3-Amino-2-bromo-6- (trifluoromethyl) pyridine This substance is related to safety and there are several things to pay attention to.
    Bear the brunt of it, it is chemically active or reacts with other substances. During operation, make sure to ventilate the environment well to prevent the accumulation of harmful gases. This is because the reaction may produce pungent and harmful gas, endangering respiratory health.
    Furthermore, contact with skin and eyes can cause irritation. Therefore, when operating, protective clothing, goggles and gloves must be worn for comprehensive protection. If you accidentally touch it, rinse it with plenty of water quickly and seek medical attention if necessary.
    In addition, the risk of explosion of this compound should not be underestimated. It should be kept away from fire and heat sources, stored in a cool, dry and ventilated place, and stored separately from oxidants, acids, etc., to avoid dangerous reactions caused by their mixing.
    When weighing and transferring, the action should be slow and accurate to prevent its dust from entering the air and being inhaled by people. After taking it, it should be properly sealed and stored to avoid moisture and oxidation-induced properties.
    Where this material is used, relevant personnel must be familiar with its safety data and emergency treatment methods. The experimental site should also be prepared with first aid equipment and medicines. In case of emergencies, it can be responded to in time. In this way, the operation is safe and accidents are avoided.