Gamma 4 Bromophenyl N N Dimethyl 2 Pyridinepropanamin Z 2 Butenedioate
pyridine pyrrole pyrazine piperidine piperazine

gamma-(4-bromophenyl)-n,n-dimethyl-2-pyridinepropanamin(z)-2-butenedioate

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    247893

    Chemical Name gamma-(4-bromophenyl)-N,N-dimethyl-2-pyridinepropanamin (Z)-2-butenedioate

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    Frequently Asked Questions

    As a leading gamma-(4-bromophenyl)-n,n-dimethyl-2-pyridinepropanamin(z)-2-butenedioate 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 γ - (4-bromophenyl) -N, N-dimethyl-2-pyridylpropylamine (Z) -2-butenediate?
    I think this question is related to the chemical structure of "γ - (4-pyridyl) -N, N-diethyl-2-aminopyridine (Z) -2-cyanodicarboxylate". This compound has a complex structure and contains a variety of functional groups.
    As an aromatic heterocycle, pyridyl groups have unique electronic properties and reactivity. The γ site connects pyridyl groups, which affects the overall electron cloud distribution and spatial configuration of the molecule. N, N-diethyl gives molecules specific lipophilicity and steric resistance, and plays a key role in intermolecular interactions and solubility. 2 -Aminopyridine moiety, the amino group is the active check point, can participate in many chemical reactions, such as nucleophilic substitution, hydrogen bond formation, etc. The conjugation of pyridine ring enhances its electron delocalization and affects the reactivity and selectivity.
    And the (Z) configuration indicates that there are double bonds in the molecule, and the groups on both sides of the double bond are arranged in a specific space. This configuration has a great influence on the physical and chemical properties of molecules, such as melting point, boiling point and optical activity. 2 -Cyanodicarboxylate moiety, the cyanyl group has strong electron absorption, which can change the electron cloud density of molecules and affect the reactivity; the structure of dicarboxylic acid ester endows the molecule with hydrolyzability and complexation with metal ions.
    In summary, the chemical structure of "γ - (4-pyridyl) -N, N-diethyl-2-aminopyridine (Z) -2-cyanodicarboxylate" interacts and collaborates to determine the unique physical and chemical properties and chemical reactivity of the molecule.
    What are the main uses of γ - (4-bromophenyl) -N, N-dimethyl-2-pyridylamine (Z) -2-butene diester?

    First, in the field of organic synthesis, it is often a key intermediate. It can be combined with many reagents through subtle reaction paths to build complex organic molecules. Due to its special chemical structure, it has an active reaction check point and can lead to various chemical transformations, such as nucleophilic substitution and esterification, paving the way for the creation of novel compounds.
    Second, in the field of medicinal chemistry, it also shows extraordinary value. Or involved in the construction of drug molecules, endowing the drug with specific pharmacological activities. By ingenious design and modification, the pharmacokinetic properties of drugs can be optimized, such as improving bioavailability and enhancing targeting, thus providing better strategies for the treatment of diseases.
    Third, in the context of materials science, it also does something. Or can participate in the synthesis of materials, endowing materials with unique physical and chemical properties. For example, improve the stability and solubility of materials, or even introduce special optical and electrical properties, so that materials can be used in electronic devices, optical materials and other fields.
    Fourth, in the process of scientific research and exploration, it provides chemical researchers with an opportunity to explore new reactions and new mechanisms. Through in-depth study of its reactivity, it can open up the boundaries of chemical knowledge, give birth to innovative chemical concepts and methods, and inject vitality into the development of chemical disciplines.
    It is based on, gamma - (4-hydroxybenzyl) -N, N-diethyl-2-to-its secondary amine (Z) -2-monobromic dianhydride, which is indispensable in many aspects such as organic synthesis, medicinal chemistry, materials science and scientific research and exploration. It is like a starry night, guiding the progress of various fields of chemistry.
    What is the preparation method of γ - (4-bromophenyl) -N, N-dimethyl-2-pyridylamine (Z) -2-butene diester?
    To prepare gamma- (4-hydroxybenzyl) -N, N-diethyl-2-pyriformamide (Z) -2-butenedioate benzyl ester, the method is as follows:
    First take an appropriate amount of raw materials and put them into the reactor in a precise ratio. In the reaction system, create suitable temperature, pressure and other conditions so that each reactant can fully interact. A specific catalyst can be selected to promote the efficient progress of the reaction. This catalyst needs to be screened to select the one with high activity and selectivity for the reaction. < Br >
    During the reaction process, various parameters need to be carefully monitored, such as temperature fluctuations, reaction time, etc. If the temperature is too high or too low, the reaction may be biased in an unexpected direction or the reaction rate may be poor. The control of time is also crucial. If it is too short, the reaction will not be fully functional, and if it is too long, it may cause side reactions, resulting in damage to the purity of the product.
    When the reaction is roughly completed, it needs to go through a series of post-processing steps. It can be extracted with a suitable solvent first to initially separate the product from the impurities. Then, by means of distillation and recrystallization, the product is further purified to obtain high-purity gamma- (4-hydroxybenzyl) -N, N-diethyl-2-pyriformamide (Z) -2-butenedioate benzyl ester.
    Each step requires fine care, and a slight pooling may affect the quality and yield of the product. From the selection of raw materials, to the regulation of reaction conditions, to the fine operation of post-processing, it is indispensable to obtain the desired product.
    What are the physical and chemical properties of γ - (4-bromophenyl) -N, N-dimethyl-2-pyridylamine (Z) -2-butene diester?
    I look at what you said about "γ - (4-hydroxybenzyl) -N, N-diethyl-2-pyridineformamide (Z) -2-acetoxybenzoate", which is an organic compound. Its physical and chemical properties are quite worthy of investigation.
    In terms of its physical properties, the compound is in a solid state at room temperature and pressure, and the specific state depends on its molecular structure and intermolecular forces. The values of its melting point and boiling point are determined by the interaction energy between molecules. If there are hydrogen bonds and van der Waals forces between molecules, the melting point and boiling point can be increased. Its solubility is also an important physical property. In organic solvents, due to the principle of similar miscibility, if its molecules have a certain polarity, or are soluble in polar organic solvents, such as ethanol, acetone, etc.; if the polarity is weak, it is more soluble in non-polar organic solvents, such as n-hexane, benzene, etc.
    As for chemical properties, its molecules contain functional groups such as pyridine ring, ester group, acetoxy group, etc. Pyridine ring has a certain alkalinity and can react with acid to form pyridine salts. The chemical properties of ester groups are active, and hydrolysis can occur under the catalysis of acids or bases. Under acidic conditions, hydrolysis generates corresponding carboxylic acids and alcohols; under alkaline conditions, hydrolysis is more thorough, forming carboxylic salts and alcohols. The acetoxy group can also be hydrolyzed under certain conditions to remove the acetyl group. In addition, if there are unsaturated bonds in the compound molecule, or an addition reaction can occur, and a variety of chemical reactions can be derived with electrophilic reagents or nucleophiles, providing rich possibilities for organic synthesis. The physical and chemical properties of this compound are determined by its unique molecular structure, which is of great significance in organic chemistry research and related fields.
    What are the safety and toxicity of γ - (4-bromophenyl) -N, N-dimethyl-2-pyridylamine (Z) -2-butenediate?
    "Gamma- (4-hydroxybenzyl) -N, N-diethyl-2-pyridineformamide (Z) -2-butene dianhydride", which is a chemical substance. Its safety and toxicity are related to many aspects.
    In terms of its safety, if it is under suitable conditions and follows the corresponding specifications, it may be safe to a certain extent. However, it behaves differently in different environments and different contact methods. If it only exists in a specific closed and controlled chemical experimental environment, and there are skilled chemists who operate according to precise procedures without extensive contact with the outside world, it is quite safe for the public. Because chemists know all kinds of prevention methods, they can avoid its leakage and volatilization, causing the surrounding environment and people to be affected.
    As for toxicity, this substance has a special structure, and its pyriformamide part may have certain biological activity. If ingested inadvertently, it may interfere with the normal biochemical reactions in the organism. It may block or change the normal physiological process due to its structure or binding to some key receptors and enzymes in the organism. Inhalation of its volatile particles may also cause irritation to the respiratory tract. Depending on the concentration, it may only feel uncomfortable or cough, and in severe cases, it may damage the normal function of the lungs. When skin contact, it may cause allergies, inflammation and other reactions. If exposed to this substance for a long time, it may cause chronic toxic effects, such as affecting the normal operation of the nervous system and immune system.
    Therefore, in order to know the exact safety and toxicity of it, rigorous scientific experiments, professional testing and analysis are required, and its impact on all levels of the organism can be carefully observed before accurate conclusions can be obtained.