Methyl 5 Aminopyridine 2 Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

methyl 5-aminopyridine-2-carboxylate

    Specifications

    HS Code

    255889

    Chemical Formula C7H8N2O2
    Molar Mass 152.15 g/mol
    Appearance Solid (usually)
    Melting Point Data may vary, check literature
    Boiling Point Data may vary, check literature
    Solubility In Water Low solubility likely
    Solubility In Organic Solvents Soluble in some organic solvents
    Density Data may vary, check literature
    Odor Typical organic compound odor
    Pka Data may vary, check literature
    Flash Point Data may vary, check literature
    Stability Stable under normal conditions

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    General Information
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    Frequently Asked Questions

    As a leading methyl 5-aminopyridine-2-carboxylate 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 chemical properties of methyl 5-aminopyridine-2-carboxylate?
    Methyl-5-aminopyridine-2-carboxylic acid ester is an important compound in organic chemistry. Looking at its chemical properties, this compound has many remarkable characteristics.
    First of all, its physical properties are mostly solid in the normal state, but its exact appearance may vary depending on purity and crystallization conditions. Its melting point, boiling point and other properties are of great significance for separation and purification. The melting point is related to the temperature node at which a substance changes from solid to liquid during heating. This property helps to determine its purity. The melting point of high-purity substances is usually fixed. The boiling point determines the temperature at which it changes from liquid to gas at a specific pressure, and is indispensable in separation operations such as distillation.
    Furthermore, its chemical properties are active. Amino and ester groups are key active functional groups. Amino groups are basic and can react with acids to form corresponding salts. This property is widely used in organic synthesis. It can be used to introduce specific groups through the reaction with acids to achieve structural modification of compounds. Ester groups can undergo hydrolysis reactions. Under acidic or alkaline conditions, ester groups are broken to form carboxylic acids and alcohols respectively. Hydrolysis is more thorough under alkaline conditions. This hydrolysis reaction is crucial in the field of organic synthesis and drug preparation. It can be used to construct compounds with specific structures or to achieve the release of active pharmaceutical ingredients.
    In addition, its pyridine ring also has unique chemical properties. The pyridine ring is rich in electrons and can undergo electrophilic substitution reactions. Under suitable conditions, other functional groups can be introduced at specific positions in the pyridine ring, which greatly enriches the structural diversity of compounds and provides the possibility for the creation of new organic compounds.
    The chemical properties of methyl-5-aminopyridine-2-carboxylic acid esters are rich and unique, and have great application value in many fields such as organic synthesis and pharmaceutical chemistry, laying a solid foundation for many chemical reactions and compound preparation.
    What are the synthesis methods of methyl 5-aminopyridine-2-carboxylate
    There are several methods for the synthesis of methyl 5-aminopyridine-2-carboxylate (methyl 5-aminopyridine-2-carboxylate).
    One of them can be obtained from the reduction reaction of methyl 5-nitropyridine-2-carboxylate. Among them, methyl 5-nitropyridine-2-carboxylate is often used as the starting material of pyridine, and the nitro group is first introduced at the 5th position of the pyridine ring by nitration reaction, and then the 5-nitropyridine-2-carboxylate is obtained by esterification reaction. Afterwards, with suitable reducing agents, such as hydrogen and metal catalysts (such as palladium carbon, platinum carbon, etc.), at appropriate temperature and pressure, the nitro group is reduced to an amino group to obtain 5-aminopyridine-2-carboxylic acid methyl ester. This process requires attention to the precise regulation of reaction conditions to avoid excessive reduction or side reactions.
    Second, 2-cyano-5-nitropyridine is used as a raw material. First, it is co-heated with methanol and acid catalysts to undergo an alcoholysis reaction, so that the cyano group is converted into an ester group to obtain 5-nitropyridine-2-carboxylic acid methyl ester, and then the nitro group is converted into an amino group by a reduction method as described above.
    There are those who use 2-methyl-5-nitropyridine as the starting material. First, the methyl group is oxidized to a carboxyl group with a mild oxidizing agent, and then esterified to obtain 5-nitropyridine-2-carboxylic acid methyl ester, and finally the nitro group is reduced to obtain the target product.
    All synthetic methods have their own advantages and disadvantages. In practical application, it is necessary to weigh and choose according to many factors such as the availability of raw materials, cost, difficulty of reaction conditions and purity of the product.
    What are the main uses of methyl 5-aminopyridine-2-carboxylate?
    Methyl-5-aminopyridine-2-carboxylic acid ester is an important compound in organic chemistry. It has a wide range of uses and has important applications in many fields.
    First, in the field of medicinal chemistry, it is often a key intermediate for the synthesis of drugs. Due to the structure of pyridine and carboxylic acid esters, it is endowed with unique chemical properties and biological activities. Drug molecules with specific pharmacological activities can be designed and synthesized through chemical modification and modification to respond to the treatment of various diseases. For example, in the synthesis of some antibacterial and anti-inflammatory drugs, it is used as a starting material to construct a therapeutic drug structure through a series of reactions.
    Second, in the field of materials science, methyl-5-aminopyridine-2-carboxylic acid esters can participate in the synthesis of polymer materials. The active groups contained in them can react with other monomers to form polymers with special properties. Such polymers may have good thermal stability, mechanical properties or optical properties, and can be used as high-performance engineering plastics, optical materials, etc., playing an important role in high-end fields such as aerospace and electronic equipment.
    Furthermore, in organic synthesis chemistry, as an important building block, it can participate in many organic reactions, such as nucleophilic substitution reactions, coupling reactions, etc. Through these reactions, more complex organic molecular structures can be constructed, providing organic synthesis chemists with rich strategies and means to synthesize organic compounds with specific structures and functions, and promoting the development of organic chemistry.
    In summary, methyl-5-aminopyridine-2-carboxylate has shown important application value in many fields such as medicinal chemistry, materials science and organic synthesis chemistry due to its unique chemical structure, which plays a positive role in promoting the development of related fields.
    What are the precautions for methyl 5-aminopyridine-2-carboxylate in storage and transportation?
    For methyl-5-aminopyridine-2-carboxylic acid esters, many matters need to be paid attention to during storage and transportation. This compound has unique properties and is easy to react when exposed to light. Its color may change and its quality may be damaged. Therefore, it should be stored in a dark brown bottle or shaded package to avoid direct exposure to light.
    Furthermore, it is quite sensitive to temperature. Under high temperature, it may cause decomposition, volatilization, and even dangerous chemical reactions; low temperature may also affect its physical state, causing it to crystallize and solidify, which is unfavorable for use. Therefore, it is best to store it in a cool place with a temperature of about 2-8 ° C.
    Humidity is also critical. Humid environment can cause methyl-5-aminopyridine-2-carboxylate to absorb moisture, or hydrolyze and deteriorate, so the storage place should be dry, and the desiccant can be placed next to it to keep it dry.
    When transporting, the packaging must be sturdy. To prevent container damage and material leakage due to shock and collision. And in accordance with relevant regulations, appropriate warning labels should be affixed to indicate its characteristics and potential hazards, so that transporters and contacts can be treated with caution.
    At the same time, this compound may be toxic and irritating, and those who store and transport it must wear protective equipment, such as gloves, goggles, protective clothing, etc., to prevent it from coming into contact with the skin and eyes, and to prevent inhalation of its volatile gas to ensure personal safety.
    What is the market outlook for methyl 5-aminopyridine-2-carboxylate?
    Methyl-5-aminopyridine-2-carboxylic acid ester, this substance is gradually emerging in the field of chemical medicine, and the prospect is promising.
    Looking at the past, the technology of organic synthesis has become increasingly exquisite. Due to its unique structure, this compound is often a key intermediate in many reactions, which has attracted the attention of many scholars. In the past, the synthesis method was complicated and inefficient, but after years of hard work, new methods have gradually emerged, and both yield and purity have improved.
    As for the market, its demand is on the rise. In pharmaceutical research and development, the creation of many types of innovative drugs often relies on this compound to build a foundation. The combination of gainpyridine ring and amino and carboxyl esters endows it with unique biological activity, which can precisely target and help new drugs attack. In the field of pesticides, it has also emerged. After ingenious modification, it can be turned into a high-efficiency and low-toxicity pesticide category, which is in line with the current trend of green agriculture.
    Furthermore, the rise of materials science also requires this product. After special processing, materials with specific functions can be prepared, which can be used in electronics, optics and other branches.
    Today, although the market size is not as large as that of traditional bulk chemicals, it is developing rapidly. Chemical companies and scientific research institutions around the world have invested in related projects, striving to expand the application boundary and improve quality and yield. With time, methyl-5-aminopyridine-2-carboxylic acid ester will definitely expand into more fields and become a shining star in the chemical industry.