10 Methoxy 1 6 Dimethylergolin 8 Yl Methyl 5 Bromopyridine 3 Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

(10-methoxy-1,6-dimethylergolin-8-yl)methyl 5-bromopyridine-3-carboxylate

    Specifications

    HS Code

    902006

    Chemical Formula C24H27BrN2O3
    Molar Mass 471.387 g/mol
    Physical State At Room Temp Solid (presumed)
    Solubility In Water Low (due to non - polar nature of ergoline part)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Uv Vis Absorption Absorption peaks likely in UV region due to conjugated systems in pyridine and ergoline rings

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    Frequently Asked Questions

    As a leading (10-methoxy-1,6-dimethylergolin-8-yl)methyl 5-bromopyridine-3-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 is the chemical structure of (10-methoxy-1, 6-dimethylergolin-8-yl) methyl 5-bromopyridine-3-carboxylate?
    The chemical structure of (10-methoxy-1,6-dimethylergoline-8-yl) methyl 5-bromopyridine-3-carboxylic acid ester is a specific compound structure in the field of organic chemistry. This structure is composed of several parts.
    The ergoline part is its core skeleton, which is connected to the methoxy group at position 10, that is, the methoxy group is connected to the carbon at position 10 of the ergoline; the 1st and 6th positions are connected to methyl groups, which is a substituent modification on the structure of the ergoline.
    The pyridine-3-carboxylic acid ester part, the pyridine ring has a carboxyl group at position 3, and the carboxyl group is connected to (10-methoxy-1,6-dimethylergoline-8-yl) methyl to form an ester bond. At position 5 of the pyridine ring, a bromine atom is attached.
    In this way, the parts are connected by chemical bonds to establish the unique chemical structure of (10-methoxy-1,6-dimethylergoline-8-yl) methyl 5-bromopyridine-3-carboxylate, which endows the compound with specific chemical properties and potential biological activities.
    What are the physical properties of (10-methoxy-1, 6-dimethylergolin-8-yl) methyl 5-bromopyridine-3-carboxylate?
    (10-Methoxy-1,6-dimethylergoline-8-yl) methyl 5-bromopyridine-3-carboxylic acid ester, this is an organic compound. Its physical properties are unique, let me tell you in detail.
    Looking at its properties, at room temperature, it may be a crystalline solid with a specific crystal structure. This structure is clearly discernible under an optical microscope, just like a finely constructed microscopic building. Its color may be white to off-white, pure without variegation, just like the purity of first snow.
    The melting point is about a certain temperature range, which is the critical value for the conversion of the compound from solid to liquid. When the external temperature gradually rises near the melting point, the lattice structure begins to loosen, the molecular movement intensifies, and finally the solid state melts into a liquid state. The accurate determination of the melting point is of great significance in identifying its purity and structural stability.
    In terms of solubility, it varies in common organic solvents. In polar organic solvents such as ethanol and dichloromethane, it may have a certain solubility, just like fish entering water, and the molecules are evenly dispersed in it. In non-polar solvents, such as n-hexane, the solubility is extremely low, similar to the incompatibility of oil and water. This difference in solubility is due to the interaction of polar and non-polar groups in the molecular structure.
    Its density is also an important physical property, and may have unique values compared with other substances. This value reflects the mass of the compound per unit volume. In chemical production and experimental operations, it is related to the amount of materials and the ratio of the reaction system.
    In addition, the compound may have a specific odor. Although it is difficult to describe accurately, it is distinguished from other compounds by its unique logo. The formation of its odor is closely related to the arrangement of atoms in the molecular structure and the vibration of chemical bonds.
    In summary, the physical properties of (10-methoxy-1,6-dimethylergoline-8-yl) methyl 5-bromopyridine-3-carboxylic acid esters lay the foundation for in-depth understanding of their chemical behavior and applications.
    What are the main uses of (10-methoxy-1, 6-dimethylergolin-8-yl) methyl 5-bromopyridine-3-carboxylate?
    (10-Methoxy-1,6-dimethylergoline-8-yl) methyl 5-bromopyridine-3-carboxylic acid ester has a wide range of uses. In the field of medicinal chemistry, it is often the key intermediate for the synthesis of special drugs. Due to its unique chemical structure, it can be converted into compounds with specific biological activities through a series of delicate chemical reactions, which is greatly helpful for the development of drugs for the treatment of specific diseases.
    In the field of organic synthesis, it is an important building block. Chemists can build more complex and diverse organic molecular structures by ingeniously modifying and modifying its structure, laying the foundation for the creation of novel organic materials.
    Furthermore, in terms of biological activity research, using this substance as a starting point to explore its mechanism of action and metabolic pathways in living organisms, or discovering new biological activity targets, which can contribute to the progress of life science. It is an indispensable and important substance for exploration and innovation in many fields such as chemistry and life science.
    What are the synthesis methods of (10-methoxy-1, 6-dimethylergolin-8-yl) methyl 5-bromopyridine-3-carboxylate?
    To prepare (10-methoxy-1,6-dimethylergoline-8-yl) methyl 5-bromopyridine-3-carboxylic acid ester, the synthesis method has the following methods.
    First, the condensation reaction can be carried out under suitable reaction conditions through the related intermediates of ergoline derivatives and 5-bromopyridine-3-carboxylic acid esters. A suitable catalyst needs to be carefully selected to promote the combination of the two. For example, the use of certain metal salt catalysts can effectively improve the reaction rate and yield. At the time of reaction, the reaction temperature and time need to be strictly controlled. If the temperature is too high or too low, it may affect the formation of the product. Generally speaking, the reaction temperature should be controlled in a specific range, and the time needs to be accurately controlled to ensure that the reaction is fully carried out without too many side reactions.
    Second, the structure of ergoline can be modified first, and suitable functional groups can be introduced to make it easier to react with 5-bromopyridine-3-carboxylate. Later, in a specific reaction system, the two interact. In this process, the choice of reaction solvent is crucial. Different solvents affect the process of the reaction and the purity of the product. It is appropriate to choose a solvent that can fully dissolve the reactants and is favorable for the reaction.
    Third, a multi-step reaction can also be considered to construct the target molecular structure. First synthesize intermediates containing part of the target structure, and then gradually connect and transform these intermediates. Each step of the reaction requires careful operation and fine regulation of the reaction conditions to ensure the smooth progress of each step, and finally successfully synthesize (10-methoxy-1,6-dimethylergoline-8-yl) methyl 5-bromopyridine-3-carboxylate. The synthesis process requires careful consideration of the feasibility, yield and purity of each step of the reaction. After repeated tests and optimization, an ideal synthesis method can be obtained.
    (10-methoxy-1, 6-dimethylergolin-8-yl) What are the precautions for methyl 5-bromopyridine-3-carboxylate during use?
    (10-Methoxy-1,6-dimethylergoline-8-yl) methyl 5-bromopyridine-3-carboxylate When using this substance, there are various things to pay attention to and must be kept in mind.
    First, it is related to safety. This substance may be toxic and irritating. When operating, be sure to wear suitable protective equipment, such as gloves, goggles, protective clothing, etc., to prevent skin contact, inhalation or accidental ingestion, to avoid physical harm. And the operation should be in a well-ventilated place, or in a fume hood, so that harmful gases can quickly disperse and ensure the safety of the operating environment.
    Second, about storage. When placed in a cool, dry, dark place, away from fire and heat sources. Due to its chemical properties or more active, improper storage is prone to deterioration, damage its effectiveness, or even risk safety. And it needs to be placed separately from oxidizing, reducing and other different properties to prevent mutual reaction.
    Third, the importance of operation. When using, accurately weigh and measure, operate according to the standard process, and must not be arbitrarily changed. If it involves steps such as dissolution and reaction, strictly control the temperature, time and proportion of reactants to ensure a smooth reaction and achieve the expected results. And the experimental equipment must be clean and dry to avoid impurities affecting the reaction.
    Fourth, waste treatment should not be underestimated. After use, the remaining substances and waste cannot be discarded at will. They should be collected and properly disposed of in accordance with relevant regulations to prevent pollution to the environment.
    In short, those who use this material must be careful in terms of safety, storage, operation and waste disposal, and follow regulations to ensure that everything goes smoothly and without mistakes.