2 Pyridinecarboxylic Acid 6 Amino Methyl Ester
pyridine pyrrole pyrazine piperidine piperazine

2-Pyridinecarboxylic acid, 6-amino-methyl ester

    Specifications

    HS Code

    870066

    Chemical Formula C7H8N2O2
    Molar Mass 152.15 g/mol
    Appearance Solid (predicted)
    Solubility In Water Limited solubility (predicted)
    Logp 0.74 (predicted)

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    General Information
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    Frequently Asked Questions

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    What is the chemical structure of 2-pyridinecarboxylic acid, 6-amino-methyl ester?
    The chemical structure of 2-% hydroxybutyric acid, 6-amino-methylpyridine, is the structural form of a specific compound in organic chemistry.
    2-% hydroxybutyric acid, whose structure is based on butyric acid. Butyric acid, a saturated fatty acid containing four carbon atoms. In the structure of butyric acid, on the second carbon atom, the hydroxyl group (-OH) replaces the hydrogen atom to form the structure of 2-% hydroxybutyric acid. The introduction of this hydroxyl group makes the molecule add the characteristics of the hydroxyl group, such as it can participate in the esterification reaction and react with acids to form ester compounds, because the hydrogen of the hydroxyl group has certain activity; and the hydroxyl group can cause the formation of hydrogen bonds between molecules, which affects the physical properties of the compound, such as boiling point, solubility, etc. Compared with butyric acid, the boiling point of 2% hydroxybutyric acid may increase due to hydrogen bonds, and the solubility in water may also increase due to the formation of hydrogen bonds between the hydroxyl group and water.
    As for 6-amino-methylpyridine, pyridine is a nitrogen-containing hexa-membered heterocyclic compound and has aromatic properties. In the sixth position of the pyridine ring (based on a specific numbering rule), there is an amino group (-NH2O) to replace the hydrogen atom, and in the methyl position of the pyridine ring (usually referring to a specific position, according to the customary number), there is a methyl group (-CH 🥰). The amino group is basic and can react with acids to form salts. Because there are lone pairs of electrons on the nitrogen atom, it can accept protons. The methyl group is an alkyl group, which has a certain electron-giving effect, which can affect the electron cloud density distribution of the pyridine ring, and then affect the reactivity of the compound. For example, in the electrophilic substitution reaction, the positioning effect of methyl and amino groups works together to determine the main position of the reaction and affect the process and product distribution of the compound participating in various organic reactions. < Br >
    These two compounds have unique structures, and each group affects each other, resulting in a variety of chemical properties and reactivity, which are of great significance in many fields such as organic synthesis and medicinal chemistry.
    What are the physical properties of 2-pyridinecarboxylic acid, 6-amino-methyl ester?
    2-% hydroxybutyric acid, 6-amino-methylpyridine, both of which are organic compounds, each with unique physical properties.
    Let's talk about 2-hydroxybutyric acid first, which is colorless to light yellow liquid under normal temperature and pressure. Smell it, it has a faint odor. Because its molecules contain hydroxyl and carboxyl groups, it has a certain polarity, exhibits good solubility in water, and can be miscible with water in any ratio. As for the melting point, it is about -20 ° C, and the boiling point is in the range of 207-208 ° C. In addition, the compound has a certain acidity, and its carboxyl groups can be ionized under specific conditions, releasing hydrogen ions.
    Let's talk about 6-amino-methylpyridine, which is normally white to light yellow crystalline powder. Looking at its appearance, the texture is fine. Smell it, it has a characteristic odor. Compared with 2-hydroxybutyric acid, its polarity is slightly weaker and its solubility in water is limited, but it has better solubility in some organic solvents such as ethanol and ether. 6-amino-methylpyridine has a relatively high melting point, roughly 50-53 ° C, and a boiling point of about 211-212 ° C. Due to the presence of amino groups in its molecules, it exhibits a certain alkalinity. Amino groups can bind hydrogen ions and play the role of bases in specific chemical reactions.
    In conclusion, 2-hydroxybutyric acid and 6-amino-methylpyridine exhibit significant differences in physical properties such as appearance, odor, solubility, melting and boiling point, and acidity and alkalinity due to molecular structural differences.
    What are the common methods for synthesizing 2-pyridinecarboxylic acids, 6-amino-methyl esters?
    2-% hydroxyl, 6-amino-methylpurine, the common adenine, has many synthesis methods, which are described in detail below.
    In the early synthesis of adenine, cyanoacetamide is often used as the starting material. Cyanoacetamide is first condensed with formamide at high temperature to generate 4-amino-5-formamido pyrimidine. This step requires control of temperature and reaction time, because although high temperature can accelerate the reaction, it is easy to cause side reactions to occur. Then, 4-amino-5-formamido pyrimidine can be obtained through cyclization, dehydration and other steps. The raw materials for this route are easy to obtain, but the reaction steps are complicated and the yield is not ideal.
    Synthesis methods using 4,5-diaminopyrimidine as raw materials are also quite common. 4,5-diaminopyrimidine reacts with formyl compounds, such as formic acid, ethyl formate, etc., under appropriate conditions to directly generate adenine. The key to this process lies in the control of the reaction conditions. The pH and temperature have a great impact on the reaction process and product purity. For example, the pH is not suitable, which makes it easy to bias the reaction to generate other pyrimidine derivatives rather than the target product adenine.
    There are also people who use purine nucleoside as raw materials and chemically modify adenine. Purine nucleoside is first hydrolyzed, desaccharide and other steps to obtain purine base, and then amino group is introduced through amination reaction, and finally adenine is obtained. The advantage of this method is that the starting material is relatively pure, the product purity is high, but the raw material cost is high, and it is not suitable for large-scale industrial production.
    With the development of organic synthesis technology, new synthesis methods are also emerging. For example, the reaction catalyzed by transition metals can synthesize adenine more efficiently and selectively. Such methods often simplify the reaction steps, improve the yield and selectivity, but also more stringent requirements for reaction equipment and operation, and the cost of transition metal catalysts is expensive, limiting its wide application.
    The methods for synthesizing adenine have their own advantages and disadvantages. In practical applications, the appropriate synthesis path should be selected according to specific needs, such as production scale, cost control, product purity requirements, etc.
    In what fields are 2-pyridinecarboxylic acids, 6-amino-methyl esters used?
    2-Hydroxybutyric acid and 6-amino-methylpyridine buzzing salt have their own uses in the fields of medicine, chemical industry, and materials.
    Let's talk about 2-hydroxybutyric acid first. In the field of medicine, because of its certain physiological activity, it has emerged in the research and development of some new drugs. Some researchers have explored using it as a starting material and synthesized novel compounds through specific chemical reactions, which are expected to become potential drugs for the treatment of nervous system diseases. In the chemical industry, 2-hydroxybutyric acid, as an important organic synthesis intermediate, can participate in the synthesis of many fine chemicals. For example, it can be esterified with alcohols under the action of catalysts to form corresponding esters. Such esters are widely used in industrial products such as fragrances and coatings, such as adding special properties to coatings or imparting a unique smell to fragrances.
    Looking at 6-amino-methyl pyridine buzzing salt, in the field of materials, with its unique structure and properties, it can be used to prepare functional polymer materials. Researchers have introduced it into polymer structures to give materials special properties such as antibacterial and electrical conductivity. For example, the prepared antibacterial polymer materials containing 6-amino-methyl pyridine buzzing salt have great application prospects in medical supplies, food packaging and other fields with strict hygiene requirements. In the field of chemical synthesis, it can be used as a high-efficiency catalyst or reaction intermediate to promote specific chemical reactions. In some complex organic compound synthesis pathways, 6-amino-methyl pyridine buzzing salt can effectively reduce the activation energy of the reaction, increase the reaction rate and yield, and promote the development of chemical synthesis technology.
    What is the market prospect of 2-pyridinecarboxylic acid, 6-amino-methyl ester?
    The market prospect of 2-% hydroxybutyric acid and 6-amino-methylpyridine is related to people's livelihood and various industries, as well as medical drugs, chemical industry and other fields. Today, it is the most important.
    2-% hydroxybutyric acid can be used as a key raw material for the synthesis of many drugs in the pharmaceutical industry. Because of its special chemical structure, it can give unique activities and properties to drug molecules. Looking at the current trend of pharmaceutical research and development, there is a growing demand for compounds with novel structures and efficacy. 2-% hydroxybutyric acid has a unique structure and is important for those who develop new drugs. And with the aging of the population, the demand for various therapeutic drugs has surged, and the market for 2-% hydroxybutyric acid as a raw material will also expand.
    In the chemical industry, 2-% hydroxybutyric acid can participate in the synthesis of a variety of fine chemicals. Fine chemicals are indispensable in industrial production and daily life. From high-end coatings to special plastics, 2-% hydroxybutyric acid has its place. With the technological innovation of the chemical industry, the requirements for raw material purity and performance are higher, and if 2-% hydroxybutyric acid can meet this demand and improve quality, its market share will increase steadily.
    As for 6-amino-methylpyridine, in the field of pesticides, it is an important intermediate for the synthesis of high-efficiency and low-toxicity pesticides. Today's agriculture pursues green, environmentally friendly and high-efficiency, and the pesticides involved in the synthesis of 6-amino-methylpyridine are in line with this trend. It can accurately remove insects and weeds, and is environmentally friendly and harmless to humans and animals. It will be favored by the majority of farmers and has a broad market prospect.
    In the field of materials science, 6-amino-methyl pyridine has also emerged. It can be used to prepare polymer materials with special functions, and such materials are in high demand in high-end fields such as electronics and aerospace. With the rapid development of science and technology, the demand for special functional materials has only increased. As a raw material for the preparation of 6-amino-methyl pyridine, its market potential is huge.
    Overall, 2-% hydroxybutyric acid and 6-amino-methyl pyridine, in response to the development needs of the times, have broad market prospects in many fields such as medicine, chemical industry, agriculture, materials, etc. Over time, they will surely shine and contribute to the development of the industry.