2 Amino 5 Bromo 6 Methypyridine
pyridine pyrrole pyrazine piperidine piperazine

2-Amino-5-bromo-6-methypyridine

    Specifications

    HS Code

    380467

    Name 2-Amino-5-bromo-6-methylpyridine
    Molecular Formula C6H7BrN2
    Molecular Weight 187.04
    Appearance Solid (Typical)
    Solubility In Water Limited solubility expected (Pyridine -amine -bromo -methyl group nature)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone (due to organic nature)
    Stability Stable under normal conditions, may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 2-Amino-5-bromo-6-methypyridine 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 chemistry of 2-Amino-5-bromo-6-methypyridine?
    2-Amino-5-bromo-6-methylpyridine, this is an organic compound. Its chemical properties are unique, including the amino group, bromine atom and methyl group contained in its structure.
    The amino group is first mentioned, and it is alkaline. Because there is no shared electron pair on the nitrogen atom, it can accept protons, so it is easy to combine with protons in acidic media to form corresponding salts. This property makes it often used as a nucleophilic reagent in organic synthesis, reacting with many electrophilic reagents, such as acyl halides, acid anhydrides, etc., to form new compounds such as amides.
    Furthermore, bromine atoms have high activity. Due to the high electronegativity of bromine, the carbon-bromine bond has a certain polarity. This bromine atom is easily attacked by nucleophiles and undergoes nucleophilic substitution reactions. For example, when reacting with sodium alcohol, bromine atoms can be replaced by alkoxy groups to form corresponding ether compounds; or when reacting with amines, new compounds containing nitrogen can be formed. And under certain conditions, it can also trigger elimination reactions, debromide hydrogen, and form unsaturated double bond structures.
    As for methyl, although relatively stable, it can affect the electron cloud distribution and spatial structure of molecules. As a power supply radical, methyl increases the electron cloud density on the pyridine ring, which in turn affects the reactivity and selectivity of the pyridine ring. In the electrophilic substitution reaction, the reaction can more easily occur at a specific position of the pyridine ring.
    In addition, the physical properties of 2-amino-5-bromo-6-methylpyridine are also related to its chemical properties. Due to the polar groups in its structure, it should have a certain solubility in some polar solvents, which is very important for the selection of the medium in which it participates in the chemical reaction. Its various chemical properties make it have potential application value in many fields such as medicine, pesticides, materials, etc., and can be used as a key intermediate for the synthesis of various functional compounds.
    What are the main uses of 2-Amino-5-bromo-6-methypyridine?
    2-Amino-5-bromo-6-methylpyridine is an extremely important chemical substance 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 create many drugs with specific biological activities. For example, when developing antibacterial drugs, its unique structure can help to construct compounds that can precisely act on specific targets in bacteria. By interacting with key proteins or enzymes in bacteria, it inhibits bacterial growth and reproduction, thereby achieving antibacterial effect.
    In the field of pesticide chemistry, 2-amino-5-bromo-6-methylpyridine also plays an important role. It can be used to synthesize pesticide products such as insecticides and fungicides. For example, through clever design and synthesis, insecticides with high selectivity and high killing power can be prepared for specific pests. By interfering with the nervous system or physiological metabolic process of pests, effective prevention and control of pests can be achieved, and the impact on the environment and non-target organisms is relatively small, which is conducive to the sustainable development of agriculture.
    In addition, in the field of materials science, it also shows potential uses. Due to the structure of the pyridine ring, the compound has unique electronic properties and stability, and can be applied to the preparation of functional materials, such as organic optoelectronic materials. By introducing it into the conjugated system, it may be able to adjust the optical and electrical properties of the material, laying the foundation for the development of new optoelectronic devices, such as organic Light Emitting Diodes (OLEDs), solar cells, etc. In summary, 2-amino-5-bromo-6-methylpyridine plays an indispensable role in many important fields due to its various uses.
    What are 2-Amino-5-bromo-6-methypyridine synthesis methods?
    To prepare 2-amino-5-bromo-6-methylpyridine, there are several common methods as follows.
    First, a suitable pyridine derivative is used as the starting material, and bromine atoms are introduced by halogenation reaction. If a pyridine with a suitable substituent is selected, under suitable reaction conditions, it is reacted with brominating reagents such as bromine, N-bromosuccinimide (NBS), etc. If bromine is used, it is often necessary to react in a suitable solvent, such as dichloromethane and carbon tetrachloride, in the presence of catalysts such as iron powder or iron tribromide. In this process, the catalyst can promote the substitution of bromine to a specific position of the pyridine ring, thereby obtaining 5-bromopyridine derivatives. Subsequently, the amino group is introduced through an amination reaction. An aminolysis reaction can be used, using liquid ammonia or organic amines as the amino source, and the bromine atom is replaced by the amino group under high temperature and pressure and the action of a suitable catalyst. In this step, the choice of catalyst is extremely critical, such as some transition metal catalysts or basic catalysts, which can effectively promote the reaction and improve the reaction efficiency and selectivity.
    Second, the pyridine ring can be constructed through a multi-step reaction to synthesize the target product. For example, using an appropriate aldehyde, ketone, amine and other compounds as raw materials, pyridine ring is constructed through condensation, cyclization and other reactions. First, a specific aldehyde and ketone undergo condensation reaction under basic conditions to form an intermediate with a certain carbon chain structure. This intermediate then reacts with amine compounds to form a pyridine ring. During the reaction process, specific substituents can be formed on the pyridine ring through the design of the raw material structure and the regulation of the reaction conditions. After that, bromination and amination reactions are carried out in the desired order, such as bromination first and then amination, to obtain 2-amino-5-bromo-6-methylpyridine.
    Furthermore, a palladium-catalyzed cross-coupling reaction strategy can also be used. First, a substrate containing a pyridine structure with suitable leaving groups, as well as a nucleophile containing bromine and amino substituents, are prepared. In the presence of palladium catalysts and ligands, the two are cross-coupled. For example, halogenated pyridine derivatives are reacted with nucleophiles such as borate esters or tin reagents containing bromine and amino groups in a suitable solvent under the action of a base. The choice of palladium catalysts and ligands has a great influence on the activity and selectivity of the reaction. The appropriate combination can precisely realize the connection of the required substituents on the pyridine ring to achieve the synthesis of 2-amino-5-bromo-6-methylpyridine.
    What is the market price of 2-Amino-5-bromo-6-methypyridine?
    2-Amino-5-bromo-6-methylpyridine, this substance is in the market, and its price often varies with time, and it also changes with quality and source. Looking at the market conditions in the past, its price fluctuates, and there is no normal pattern.
    In the past, in the chemical industry markets, the supply and demand of materials, the progress of technology and innovation, are all factors that change the price. If raw materials are widely available, but the demand is not abundant, the price may stabilize, or there may be a tendency to decline; if there are many people in need, and there is a shortage of supply, the price will rise.
    In addition, the difference in its quality is also the key to the price. Those who are refined and flawless must be more expensive than those who are miscellaneous. And different places of origin, due to the difference in process and cost, the price is also different. Or it is produced in a distant place, and the price increases due to the cost of freight.
    Today, if you want to confirm the price, you should consult the merchants of chemical materials, or explore the platform for chemical transactions. Only then can you get the current actual price, and take the state of the bright market as the basis for business.
    2-Amino-5-bromo-6-methypyridine What are the precautions during storage and transportation?
    2-Amino-5-bromo-6-methylpyridine is a kind of organic compound. During storage and transportation, many matters must be paid attention to.
    First words storage. This compound should be placed in a cool, dry and well-ventilated place. Because if the substance is heated, it may change its chemical properties or even cause adverse consequences such as decomposition. In case of hot topic, there may be a risk of combustion or explosion. Therefore, it is the first priority to stay away from fire and heat sources. And it must be avoided from contact with oxidizing agents, acids and other substances. If these substances meet with it, it is easy to cause chemical reactions, damage the quality of the compound, or be dangerous. It is advisable to store it in a sealed container to prevent it from interacting with moisture and oxygen in the air and causing deterioration.
    As for transportation. Before transportation, ensure that the packaging is intact. The packaging materials used must be able to resist vibration, collision and friction to prevent damage and leakage during transportation. During transportation, a suitable temperature and humidity environment should also be maintained, and it should not be exposed to extreme conditions. And the transportation vehicle should be equipped with corresponding fire fighting equipment and leakage emergency treatment equipment, just in case. The escort personnel must also be familiar with the characteristics of the compound and emergency treatment methods. In case of emergencies, they can be properly disposed of in time.
    In summary, when storing and transporting 2-amino-5-bromo-6-methylpyridine, strict attention should be paid to the environment, packaging, protection and personnel to ensure its safety and quality.