2 4 5 6 Tetradeuteriopyridine 3 Carboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

2,4,5,6-tetradeuteriopyridine-3-carboxylic acid

    Specifications

    HS Code

    325702

    Chemical Formula C6D4NO2H
    Molecular Weight 128.15
    Appearance Solid (Typical appearance of the product)
    Melting Point Specific value if known
    Boiling Point Specific value if known
    Solubility In Water Solubility details
    Solubility In Organic Solvents Details on solubility in common organic solvents
    Density Value if available
    Pka Value Value relevant to its acidic nature
    Stability General stability description

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    General Information
    Where to Buy 2,4,5,6-tetradeuteriopyridine-3-carboxylic acid in China?
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    Frequently Asked Questions

    As a leading 2,4,5,6-tetradeuteriopyridine-3-carboxylic acid 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 2,4,5,6-tetradeuterated pyridine-3-carboxylic acid?
    2% 2C4% 2C5% 2C6-tetrahydropyridine-3-carboxylic acid, this compound has important uses in many fields.
    In the field of medicinal chemistry, it is often involved in drug synthesis as a key intermediate. The construction of many drug molecules relies on it to build a specific structural framework and help form biologically active pharmacophore. For example, when developing drugs for the treatment of neurological diseases, 2% 2C4% 2C5% 2C6-tetrahydropyridine-3-carboxylic acid can provide a suitable spatial structure and chemical activity check point for the drug, so that the drug can better bind to neural receptors, and then regulate the transmission of neurotransmitters to achieve the purpose of treating diseases. < Br >
    In organic synthetic chemistry, it is an extremely useful synthetic building block. With its unique molecular structure and reactivity, it can react with other organic compounds through a variety of chemical reactions, such as nucleophilic substitution, oxidation reduction, etc., to build more complex and diverse organic molecules. For example, when building natural product analogs with specific functions, it can be used as a starting material to gradually build structures similar to natural products through multi-step reactions, providing a material basis for the study of the biological activity and mechanism of action of natural products.
    In materials science, its derivatives can be used to prepare functional materials. For example, by copolymerizing it with a specific polymer monomer, polymeric materials can be endowed with special properties, such as improving their solubility, thermal stability, or optical activity, thus expanding their applications in optics, electronics, and other fields.
    What are the synthesis methods of 2,4,5,6-tetradeuterated pyridine-3-carboxylic acid?
    To prepare 2,4,5,6-tetrahydropyridazine-3-carboxylic acid, there are several methods:
    First, with suitable starting materials, a pyridazine ring is constructed through a multi-step reaction and carboxyl groups are introduced. Compounds containing suitable substituents can be selected first, and condensation and cyclization steps common in organic reactions can be used. For example, with raw materials with corresponding carbon chains and active groups, under suitable reaction conditions and catalysts, a condensation reaction is carried out to form a pyridazine ring structure. Then, carboxyl groups are introduced at suitable positions through specific carboxylation reactions. This process requires precise control of reaction conditions, such as temperature, pH, reaction time, etc., to ensure that the reaction proceeds in the expected direction and improve the yield and purity of the product.
    Second, a stepwise synthesis strategy can also be considered. First synthesize the pyridazine ring parent, and then gradually modify it to introduce the required substituents and carboxylic groups. Initially, the basic structure of the pyridazine ring can be synthesized through classical organic synthesis reactions, such as nucleophilic substitution, electrophilic substitution, etc. Subsequently, according to the required substitution mode, select suitable reaction reagents and conditions, introduce hydrogen atoms and other substituents at specific positions, and gradually construct the structure of 2,4,5,6-tetrahydropyridazine. Finally, through suitable carboxylation methods, carboxyl groups are introduced into the target position to achieve the synthesis of 2,4,5,6-tetrahydropyridazine-3-carboxylic acid.
    Third, we can also learn from the synthesis methods of similar compounds reported in the literature, and improve them according to the structural characteristics of the target products. Refer to the previous experience in the synthesis of pyridazines or carboxyl heterocyclic compounds to optimize the reaction route and conditions. It may involve the selection of reaction intermediates, the adjustment of reaction sequence, and the use of new catalysts or reagents to simplify the synthesis steps, improve the reaction efficiency and selectivity, so as to efficiently synthesize 2,4,5,6-tetrahydropyridazine-3-carboxylic acid.
    What are the physical properties of 2,4,5,6-tetradeuterated pyridine-3-carboxylic acids?
    2% 2C4% 2C5% 2C6-tetrahydropyridine-3-carboxylic acid, this is an organic compound. Its physical properties are as follows:
    Looking at its morphology, at room temperature, it is mostly in the state of white to light yellow crystalline powder, with fine texture and fine granular appearance.
    Smell its smell, usually without significant pungent or special odor, the smell is peaceful, and it is difficult to detect obvious odor emission in general environments.
    Measure its melting point, which is about a certain temperature range. The specific value varies slightly due to purity and other factors, roughly between [X] ° C - [X] ° C. This temperature range is the critical range for the transformation of the substance from solid to liquid. < Br >
    In terms of its solubility, it has a certain solubility in water, and can partially or completely disperse and dissolve under the action of water molecules to form a uniform and stable solution, but the solubility is not very high; in common organic solvents such as ethanol, acetone, etc., it also shows different degrees of solubility. The solubility in ethanol is relatively good, and it can be well miscible. This property is closely related to the functional groups contained in its molecular structure and the overall polarity.
    Looking at its stability, under conventional environmental conditions, in a dry and cool place, it can maintain a relatively stable chemical structure and physical form, and is not prone to spontaneous significant chemical changes. However, when exposed to extreme chemical environments such as strong acids and alkalis, or special physical conditions such as high temperature and high humidity, its molecular structure may be damaged, and chemical reactions may occur, resulting in changes in physical properties.
    What is the price range of 2,4,5,6-tetradeuterated pyridine-3-carboxylic acid in the market?
    The question I heard you asked is about the price range of 2,4,5,6-tetrahydropyridazine-3-carboxylic acid in the market. However, the price of this drug varies for many reasons, and it is difficult to determine the number.
    First, the supply and demand of the market, if there are many applicants and few suppliers, the price will be raised; if the supply exceeds the demand, the price will be depressed. Second, the producers are different, and their skills are different from their own, resulting in different prices. Large factories have excellent skills and large regulations, and the cost may be low, and the price may be close to the people; small factories are the opposite. Third, the amount of purchase also affects the price. If the batch purchase volume is large, the price may be concessional; if the retail purchase quantity is small, the price may be high.
    In addition, the quality of medicine is related to the price. Those who are pure and high-quality are expensive, but the price is low. And the economic conditions and tax policies of different places are different, which also makes the price vary from domain to domain.
    In summary, if you want to know the exact price, you need to check it carefully in the time and market, consult the merchants and the merchants, or you can know the approximate price range.
    What are the storage conditions for 2,4,5,6-tetradeuterated pyridine-3-carboxylic acid?
    The storage conditions of 2% 2C4% 2C5% 2C6-tetrahydropyridine-3-carboxylic acid are related to the suitable storage conditions of this compound, which is the key to maintaining its chemical properties and quality.
    Husband 2% 2C4% 2C5% 2C6-tetrahydropyridine-3-carboxylic acid should be stored in a cool, dry and well-ventilated place. In a cool place, due to high temperature, it is easy to cause chemical reactions of this compound, or cause it to decompose or deteriorate. The temperature should be controlled within a specific range, usually not exceeding [X] ° C, which can reduce its molecular activity and inhibit unnecessary chemical changes.
    Dry environment is also indispensable. If this compound encounters water vapor or undergoes reactions such as hydrolysis, its structure and properties will be damaged. Therefore, the storage place should be protected from moisture and the humidity should be maintained below [X]%. Auxiliary means such as desiccants can be used to keep the environment dry.
    Well-ventilated allows air circulation in the storage space to avoid local gas accumulation, which can cause abnormal concentrations of oxygen, water vapor and other components in the environment and affect the stability of the compound.
    Furthermore, when storing this substance, it should be isolated from oxidants, acids, bases and other substances. The chemical properties of this compound make it easy to react with such substances. Oxidants may initiate oxidation reactions, while acids and bases may catalyze hydrolysis or other chemical reactions, causing the compound to deteriorate.
    And the storage container should also be carefully selected. When using corrosion-resistant and well-sealed containers, such as glass containers or specific plastic containers, to avoid the interaction between the container and the compound, and to ensure that the container is sealed to prevent the intrusion of outside air, water vapor, etc.
    In short, following these storage conditions, it is necessary to properly store 2% 2C4% 2C5% 2C6-tetrahydropyridine-3-carboxylic acid, so that it can maintain good chemical properties and quality in subsequent use.