2 3 Formyl 4 2 Methylpropoxy Phenyl 4 Methyl 5 Thiazolecarboxylic Acid Ethyl Ester
quinoline thiophene imidazole thiazole

2-[3-Formyl-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester

    Specifications

    HS Code

    746640

    Chemical Name 2-[3-Formyl-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester

    As an accredited 2-[3-Formyl-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Storage
    Shipping
    Free Quote

    Competitive 2-[3-Formyl-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to info@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: info@alchemist-chem.com

    General Information
    Where to Buy 2-[3-Formyl-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester in China?
    As a trusted 2-[3-Formyl-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 2-[3-Formyl-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    2- [3-Formyl-4- (2-methylpropoxy) phenyl] -4-methyl-5-thiazolecarboxylic acid ethyl ester
    This is the chemical structure analysis of 2- [3-formyl-4- (2-methylpropoxy) phenyl] -4-methyl-5-thiazole carboxylic acid ethyl ester.
    Looking at its name, it can be seen that this compound is composed of many parts. First of all, the thiazole ring is a five-membered heterocyclic ring containing nitrogen and sulfur, with specific substituents attached to it. In the second position of the thiazole ring, there is a complex phenyl structure connected. The third position of the phenyl group is formyl (-CHO), and the fourth position is connected with 2-methylpropoxy (- (CH) -2 CH (CH) ³). The existence of this oxygen group adds a specific spatial structure and chemical properties to the molecule. The fourth position of the thiazole ring is methyl (-CH), and the fifth position is connected with a carboxylic acid ethyl ester group (-COOCH). The characteristics of this ester group also affect the physical and chemical properties of the whole molecule.
    In summary, the chemical structure of 2 - [3 - formyl - 4 - (2 - methylpropoxy) phenyl] - 4 - methyl - 5 - thiazole ethyl carboxylate is composed of thiazole ring and its formyl group at specific positions, methyl group, 2 - methylpropoxy group and ethyl carboxylate group, etc. Each part interacts to endow the compound with unique chemical properties and reactivity.
    What are the physical properties of 2- [3-Formyl-4- (2-methylpropoxy) phenyl] -4-methyl-5-thiazolecarboxylic acid ethyl ester
    2-% 5B3-formyl-4- (2-methylpropoxy) phenyl% 5D-4-methyl-5-thiazole carboxylic acid ethyl ester, this is an organic compound. Looking at its structure, it is formed by the interconnection of complex groups. Its physical properties are quite important and are related to many practical applications.
    First talk about the appearance, under room temperature and pressure, or in a solid state, it is often white or off-white crystalline powder, which is caused by the intermolecular forces and arrangements. As for the melting point, due to the presence of a variety of groups in the molecule, the interaction is complex, so the melting point may be in a specific range, it is speculated, or between 100 ° C and 150 ° C, and the hydrogen bonds, van der Waals forces, etc. between the groups interact, so that the molecule needs to absorb a specific energy to overcome the lattice energy and melt.
    In terms of solubility, the compounds exhibit various properties in organic solvents. In polar organic solvents, such as ethanol and acetone, it may have a certain solubility. Due to the polarity of some groups in the molecule, it can form interactions with polar solvent molecules, such as hydrogen bonds, dipole-dipole interactions, etc.; in non-polar organic solvents, such as n-hexane, the solubility may be extremely low, because the molecule as a whole is not completely non-polar, and the intermolecular force with the non-polar solvent is weak.
    In addition, the density of the compound may be similar to that of common organic compounds, about 1.1-1.3 g/cm ³, which is determined by the molecular composition and spatial arrangement. Its volatility is low, and the intermolecular force is strong, making it difficult to transition from liquid to gaseous and escape. < Br >
    The physical properties of this compound are of great significance in the fields of organic synthesis, drug development, etc. Knowing its physical properties can provide an important basis for related research and applications.
    What is the synthesis method of 2- [3-Formyl-4- (2-methylpropoxy) phenyl] -4-methyl-5-thiazolecarboxylic acid ethyl ester
    The synthesis method of 2-% 5B3-formyl-4- (2-methylpropoxy) phenyl% 5D-4-methyl-5-thiazole carboxylic acid ethyl ester can follow the following steps:
    First take an appropriate amount of 4- (2-methylpropoxy) -3-nitrobenzaldehyde, place it in a reactor, add an appropriate amount of solvent, such as dichloromethane, etc., stir to dissolve it. In this solution, a specific reducing agent, such as sodium borohydride, is slowly added to maintain a certain temperature, about 0 ° C to 5 ° C, and the reaction is continuously stirred for a number of times, so that the nitro group can be successfully reduced to the amino group to obtain 4- (2-methylpropoxy) -3-aminobenzaldehyde.
    The obtained 4- (2-methylpropoxy) -3-aminobenzaldehyde is placed in another reaction vessel with 2-bromo-3-oxobutyrate ethyl ester, an appropriate amount of base, such as potassium carbonate, and then acetonitrile is used as a solvent to heat the reflux reaction. In this process, the amino group and the carbonyl group of 2-bromo-3-oxobutyrate ethyl ester undergo a series of reactions such as nucleophilic substitution. After several times of reaction, the reaction solution was cooled. After
    , the cooled reaction solution was separated and purified. First, the solvent was removed by a rotary evaporator, and then the column chromatography was performed to select a suitable eluent, such as petroleum ether and ethyl acetate mixed in a certain proportion, to separate the pure 2-% 5B3-formyl-4- (2-methylpropoxy) phenyl% 5D-4-methyl-5-thiazole carboxylic acid ethyl ester crude product. The crude product is recrystallized with a suitable solvent, such as ethanol-water mixed solvent, to obtain a high-purity target product.
    This synthesis method has clear steps and easy to control the reaction conditions of each step. However, in actual operation, the conditions need to be fine-tuned according to the specific situation to achieve the best synthesis effect.
    2- [3-Formyl-4- (2-methylpropoxy) phenyl] -4-methyl-5-thiazolecarboxylic acid ethyl ester
    2-% 5B3-formyl-4- (2-methylpropoxy) phenyl% 5D-4-methyl-5-thiazole carboxylic acid ethyl ester, which is widely used. In the field of medicinal chemistry, it can be used as a key intermediate for the creation of new drugs. Geinthiazole and benzene ring structures are common in many drug molecules, and have unique biological activities and pharmacological properties. They can interact with specific targets in organisms, or regulate physiological processes, or fight diseases.
    In the field of materials science, such compounds may be used to prepare special functional materials. Due to the various functional groups contained in the molecule, it can be chemically modified and modified to endow the material with special properties, such as optical, electrical or thermal properties, and then applied to optical materials, electronic devices and other fields.
    In organic synthesis chemistry, as an important synthetic block, it relies on the reactivity of different functional groups to construct organic compounds with more complex and diverse structures through various organic reactions, which contributes to the development of organic synthesis methodologies and the creation and exploration of new compounds.
    In summary, 2-% 5B3-formyl-4- (2-methylpropoxy) phenyl% 5D-4-methyl-5-thiazole carboxylate ethyl ester has important potential applications in many fields such as medicine, materials and organic synthesis.
    2- [3-Formyl-4- (2-methylpropoxy) phenyl] -4-methyl-5-thiazolecarboxylic acid ethyl ester
    2-% 5B3-formyl-4-% 282-methylpropoxy% 29 phenyl% 5D-4-methyl-5-thiazole carboxylic acid ethyl ester, this compound has considerable market prospects.
    It has potential medicinal value in the field of medicine. Due to its unique chemical structure, it may be used as a key intermediate for the development of new drugs. At present, the pharmaceutical industry is eager for innovative drugs. This compound may emerge in the creation of anti-inflammatory and anti-tumor drugs, providing a new way to overcome many difficult diseases.
    In the field of materials science, there is also an opportunity for development. With the rapid development of science and technology, the demand for special performance materials is increasing day by day. Some chemical properties of the compound may make it useful in the preparation of functional materials, such as for the preparation of materials with special optical and electrical properties, to meet the needs of high-end fields such as electronics and optics.
    However, its market expansion also faces challenges. The complexity of the synthesis process results in high production costs. To be widely used in the market, researchers need to make every effort to optimize the synthesis route and reduce costs. And market awareness needs to be improved. More research and promotion are needed to make relevant industries aware of its potential value in order to open up a broader market space. In short, although there are many challenges, the potential is huge. With time and effort, it is expected to occupy an important position in the market.