Methyl 1 2 5 6 Tetrahydro 1 Methyl 3 Pyridinecarboxylate Hydrobromide
pyridine pyrrole pyrazine piperidine piperazine

methyl 1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxylate hydrobromide

    Specifications

    HS Code

    599348

    Chemical Formula C7H12BrNO2
    Molecular Weight 222.08
    Appearance Solid (Typical)
    Physical State Solid
    Solubility Soluble in some organic solvents
    Melting Point Data may vary by source
    Boiling Point Data may vary by source
    Density Data may vary by source
    Ph Data may vary depending on solution
    Stability Stable under normal conditions, but check reactivity with other substances
    Hazardous Nature May have certain health and safety hazards; check SDS

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    General Information
    Where to Buy methyl 1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxylate hydrobromide in China?
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    Frequently Asked Questions

    As a leading methyl 1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxylate hydrobromide 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 chemical structure of methyl 1, 2, 5, 6 - tetrahydro - 1 - methyl - 3 - pyridinecarboxylate hydrobromide?
    "Methyl + 1, 2, 5, 6 - tetrahydro - 1 - methyl - 3 - pyridinecarboxylate hydrobromide", which is the name of the chemical substance. According to the chemical naming rules. "Methyl" means methyl, which is often a group of one carbon and three hydrogens in the chemical structure. "1, 2, 5, 6 - tetrahydro" indicates that the compound undergoes hydrogenation at the 1, 2, 5, and 6 positions, that is, the unsaturated bond at this position is saturated by hydrogen addition. "1 - methyl" indicates that there is a methyl group attached at the 1 position. "3 - pyridinecarboxylate" refers to the carboxylic acid ester group attached to the 3 position of the pyridine ring. Pyridine is a nitrogen-containing six-membered heterocycle and has aromatic properties. And "hydrobromide" indicates that the compound forms hydrobromide.
    In summary, the chemical structure of this compound is roughly as follows: with the pyridine ring as the core, at the 1-position monomethyl, at the 3-position carboxylic acid ester group, the unsaturated bonds at the 1, 2, 5, and 6 positions are hydrogenated and saturated, and the whole is hydrobromide. In this way, the appearance of its chemical structure is gradually becoming clear.
    What are the main uses of methyl 1, 2, 5, 6 - tetrahydro - 1 - methyl - 3 - pyridinecarboxylate hydrobromide?
    Methyl-1,2,5,6-tetrahydro-1-methyl-3-pyridyl carboxylate hydrobromide has a wide range of uses. In the field of medicine, it can be used as a key intermediate to help synthesize many compounds with specific biological activities, such as some drugs with potential therapeutic effects on neurological diseases. In the field of organic synthesis, it is like a cornerstone, providing support for the construction of complex pyridine compound architectures. Through specific reactions, products with diverse structures can be derived to enrich the variety of organic compounds. At the level of scientific research and exploration, researchers use its unique structural characteristics to explore novel reaction pathways and mechanisms, and promote the progress of organic chemistry theory and technology. Due to its unique chemical properties, this compound plays an important role in the fields of pharmaceutical research and development, organic synthesis, and scientific research innovation, and is like a key to unlocking the door to progress in the fields of chemistry and medicine.
    What is the synthesis method of methyl 1, 2, 5, 6 - tetrahydro - 1 - methyl - 3 - pyridinecarboxylate hydrobromide?
    To prepare methyl-1,2,5,6-tetrahydro-1-methyl-3-pyridyl carboxylate hydrobromide, the method is as follows:
    First take a suitable pyridine derivative as the starting material, this derivative needs to have a modifiable group to facilitate subsequent reactions. In a specific reaction environment, add appropriate reagents and catalysts to create conditions to promote the reaction.
    Can be alkylated first, so that methyl groups are introduced at specific positions on the pyridine ring. This step requires precise control of the reaction temperature and time, and selection of appropriate alkylation reagents to ensure that the reaction proceeds in the desired direction.
    Then the hydrogenation reaction is carried out, and the partially unsaturated bond of the pyridine ring is reduced to obtain the 1,2,5,6-tetrahydropyridine structure. In this step, the choice of catalyst is the key, and its activity and selectivity are related to the purity and yield of the product.
    After esterification, the carboxylic acid ester group is introduced at the 3-position. This process requires attention to the pH of the reaction system and the selection of solvents to improve the reaction efficiency.
    After the above steps are completed, methyl-1,2,5,6-tetrahydro-1-methyl-3-pyridine carboxylate is obtained.
    Finally, the product is reacted with hydrobromic acid, and through the salt-forming process, methyl-1,2,5,6-tetrahydro-1-methyl-3-pyridyl carboxylate hydrobromide can be obtained. After each step of the reaction, it needs to be separated and purified to ensure the purity of the product before proceeding to the next step of the reaction. In this way, the target product can be obtained.
    What are the physical properties of methyl 1, 2, 5, 6 - tetrahydro - 1 - methyl - 3 - pyridinecarboxylate hydrobromide?
    Methyl-1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxylate hydrobromide, this is an organic compound. Its physical properties are unique and are described in detail by you.
    Looking at its appearance, it is often white to off-white crystalline powder, just like the fine snow that falls at the beginning of winter, delicate and pure, and its slightly flickering luster may be seen in sunlight.
    As for solubility, the compound is slightly soluble in water, like a light feather, drifting in water for a while, only slightly blending into it; but it is easily soluble in organic solvents, such as ethanol, chloroform, etc. In organic solvents, it is like a fish in water, quickly dissipating and fusing to form a uniform solution.
    When it comes to the melting point, its melting point is within a specific range. When the temperature gradually rises to a certain precise point, the compound begins to slowly transform from solid to liquid, like ice and snow in spring, quietly melting. This melting point is of great significance for the identification and purification of the substance and is one of its important physical markers.
    In addition, the stability of the compound is also a key physical property. Under normal temperature and pressure and dry environment, it can still maintain its own structure and properties. However, in case of high temperature, high humidity, or contact with specific chemical substances, chemical reactions may occur, causing changes in its structure and properties.
    The physical properties of this compound have a profound impact on the fields of organic synthesis and drug development. Scientists often design experimental procedures rationally according to their properties to achieve the expected scientific research purposes.
    Methyl 1,2,5,6 - tetrahydro - 1 - methyl - 3 - pyridinecarboxylate hydrobromide What are the precautions in storage and transportation?
    Methyl-1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxylate hydrobromide is a chemical substance. When storing and transporting, pay attention to the following numbers:
    First, the storage environment must be cool, dry and well ventilated. This substance is afraid of moisture and heat, and it is easy to deteriorate and damage its chemical properties in a high temperature and humid environment. If placed in a dark and dry place, its stability can be guaranteed.
    Second, it needs to be stored separately from oxidants, acids, bases, etc. Because of its active chemical properties, it can mix with the above substances, or react chemically, causing danger, such as fire, explosion, etc. It must be properly classified and placed to prevent accidents.
    Third, the storage place should be prepared with suitable materials to contain leaks. If there is a leak, it can be collected with inert materials such as sand and vermiculite, and then properly disposed of to avoid polluting the environment and endangering personal safety.
    Fourth, during transportation, make sure that the container does not leak, collapse, fall, or damage. Load lightly and unload lightly, prevent vibration and collision, keep the packaging intact, and avoid material leakage.
    Fifth, when transporting, you should follow the specified route and do not stop in densely populated areas and residential areas. If there is a sudden, densely populated areas will cause great harm, and the risk can be reduced according to the specified route.