2 Thiophenepropanoicacid Methylester
quinoline thiophene imidazole thiazole

2-Thiophenepropanoicacid,methylester

Taiy Chemical

    Specifications

    HS Code

    459607

    Chemical Formula C7H8O2S
    Molar Mass 156.203 g/mol
    Appearance Clear to slightly yellow liquid
    Boiling Point Around 220 - 225 °C
    Density Approx. 1.19 g/cm³
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in many organic solvents like ethanol, ether
    Flash Point Approx. 92 °C
    Vapor Pressure Low at room temperature

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    General Information
    Where to Buy 2-Thiophenepropanoicacid,methylester in China?
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    Frequently Asked Questions

    As a leading 2-Thiophenepropanoicacid,methylester supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main uses of methyl 2-thiophenylpropionate?
    Ethyl 2-% pentanedioate has a wide range of main uses. In the field of medicine, this is an important organic synthesis intermediate and can be used to prepare a variety of drugs. For example, in the synthesis of some nervous system drugs, it is a key raw material. After a series of chemical reactions, it can build molecular structures with specific pharmacological activities and help relieve the symptoms of neurological diseases.
    In the chemical industry, it plays an important role in the synthesis of fragrances. With its unique chemical properties, it participates in the construction of fragrance molecules, giving fragrances a unique aroma. For example, when blending some fresh and natural-style fragrances, 2-% ethyl pentanedioate can contribute to a unique odor level, enhancing the quality and uniqueness of fragrances.
    In agriculture, it can be used to synthesize some plant growth regulators. These regulators have a significant impact on the growth and development of crops, can regulate the flowering and fruiting time of crops, and improve crop resistance, such as enhancing the resistance of crops to adverse environments such as drought and cold, thereby increasing crop yield and quality.
    In addition, in organic chemistry research, 2-% pentanedioate ethyl ester is often used as a model compound for researchers to explore the mechanism and laws of chemical reactions. Due to its structural characteristics, it can provide a lot of valuable information for the study of organic reactions, help scientists to deeply understand the reaction process, optimize reaction conditions, develop new synthesis methods, and promote the continuous development of organic chemistry.
    What are the physical properties of methyl 2-thiophenylpropionate?
    2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF%E8%80%85, is a kind of organic compound. It has unique physical properties and is widely used in many fields.
    Under normal temperature and pressure, the 2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF is often colorless and transparent liquid, with clear texture and pure visual perception. Its smell has a specific aromatic smell. Although this smell is not pungent, it is recognizable and can be identified in a specific environment.
    When it comes to volatility, the volatility of this compound is relatively moderate. It does not seem that some substances evaporate quickly, nor is it extremely difficult to evaporate. Moderate volatility makes it possible to better control its concentration and existence time in the environment during a specific process operation, providing convenience for related production and application. The boiling point of 2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF is also an important physical property. Its boiling point is in a certain numerical range, which determines its behavior during operations such as heating or distillation. Under the corresponding temperature conditions, it can realize the transition from liquid to gaseous state, and then use it in chemical processes such as separation and purification.
    In terms of solubility, 2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF soluble in a variety of organic solvents. Common organic solvents such as ethanol and ether have good miscibility with them. This property makes it often used as a solvent in organic synthesis reactions to help the reactants fully mix and contact, and promote the smooth progress of the reaction. However, its solubility in water is poor, and when mixed with water, it is prone to stratification. The upper layer is an organic phase, and the lower layer is an aqueous phase.
    Density is also a factor in considering the physical properties of 2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF. Its density is higher or lower than that of water, and this difference is of great significance in some operations involving liquid-liquid separation. Operators can achieve separation purposes by means of methods such as gravity sedimentation according to the density of it and other liquids.
    In summary, the physical properties of 2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF, such as properties, odor, volatility, boiling point, solubility and density, are interrelated and play their own roles. They are key considerations in many fields such as chemical industry, medicine, scientific research, etc., and are of great significance for their application and research.
    Is the chemical property of methyl 2-thiophenylpropionate stable?
    2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF, this is an organic compound. The stability of its chemical properties must be analyzed from multiple ends.
    First of all, its structure. This compound has a specific molecular structure, composed of specific atoms in a specific way of bonding. The strength and type of its chemical bonds have a great impact on the stability. Carbon-carbon bonds and carbon-oxygen bonds, etc., each have their own inherent bond energy. If the bond energy is higher, more energy is required to break the bond, and the molecule is more stable. 2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF various chemical bonds interact to jointly maintain the stable form of the molecule.
    times and external conditions. When the temperature rises, the thermal motion of the molecule intensifies and the energy is increased. If the energy is sufficient to overcome the binding of the chemical bond, the bond may be broken and the stability will decrease. If it is in a high temperature environment, 2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF or decomposition, rearrangement and other reactions may occur. At low temperatures, the thermal motion of the molecule weakens and the stability is relatively improved.
    Furthermore, the chemical environment is also critical. In case of specific chemical reagents, 2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF or react with them. If there are strong oxidizing agents or strong reducing agents in the environment, it may cause oxidation-reduction reactions, change its molecular structure, and damage its stability. However, in an inert environment, such as a system filled with inert gases such as nitrogen, it is less disturbed by external chemical effects, and the stability can be maintained.
    In general, the chemical stability of 2-%E5%99%BB%E5%90%A9%E4%B8%99%E9%85%B8%E7%94%B2%E9%85%AF is not absolute and can remain relatively stable under specific conditions. However, when external factors change, the stability may also change.
    What are the preparation methods of methyl 2-thiophenylpropionate?
    To prepare 2-pentanone ethyl butyrate, the method is as follows:
    First, it can be obtained by Clyson condensation reaction. Take ethyl acetate and ethyl butyrate, and under the action of alkaline catalysts such as sodium alcohol, the α-hydrogen of ethyl acetate is attacked by alkali, and carbon negative ions are generated. This carbon negative ion initiates nucleophilic addition to the carbonyl group of ethyl butyrate, and then eliminates the ethoxy group to obtain 2-pentanone ethyl butyrate. This reaction needs to be carefully operated in an anhydrous and low temperature environment to prevent side reactions from breeding. The key lies in the control of the amount of basic catalyst and the reaction temperature. If the conditions are not right, it is easy to cause the product to be impure. < Br >
    Second, ethyl acetoacetate can also be obtained as a starting material. First, ethyl acetoacetate interacts with a base to form an enol anion, and then nucleophilic substitution with ethyl halobutyrate, and ethyl butyrate fragments are introduced. After hydrolysis and decarboxylation, it can be converted into the target product 2-pentanone ethyl butyrate. The key to this path lies in the selectivity of nucleophilic substitution reactions and the precise regulation of hydrolysis and decarboxylation conditions. Pay attention to acid-base strength and reaction time during hydrolysis, and control the temperature and reaction time for decarboxylation to obtain a pure product.
    Third, the organometallic reagent method can also be used. Using ethyl butyrate as the starting material, the corresponding intermediates such as enol lithium salt or enol borate are first prepared, and then nucleophilic acyl substitution reaction occurs with acetyl halide. The activity of organometallic reagents is quite high, and the sensitivity to water and air should be paid attention to during the reaction process. It needs to be operated in an anhydrous and anaerobic environment, and the regulation of the reaction temperature and the ratio of reagents is also an important link, so as to improve the yield and purity of the product.
    What are the precautions for methyl 2-thiophenylpropionate in storage and transportation?
    For 2-% ethyl pentanediate, many matters need to be paid attention to during storage and transportation.
    First temperature control. This compound may change due to temperature, and high temperature can easily cause its reaction to intensify, or cause decomposition changes, which will damage its quality. Therefore, it should be stored in a cool place. When transporting, it is also necessary to avoid high temperature environments. Temperature-controlled transportation vehicles are often used to keep it stable.
    Second is the prevention of humidity. Moisture may interact with 2-% ethyl pentanediate, causing reactions such as hydrolysis to cause it to deteriorate. The storage place should be dry and moisture-free, and the transportation packaging should also have moisture-proof ability. For example, it should be wrapped in moisture-proof materials, or a desiccant should be placed in the packaging.
    Furthermore, avoid mixed contact with sundries. Ethyl 2-% pentanediate may react chemically with other substances, causing performance changes and quality degradation. During storage and transportation, it should not be mixed with oxidants, reducing agents, strong acids and alkalis, etc., and should be placed separately to ensure isolation.
    The solidity of the packaging is also important. Stable packaging can avoid container damage due to vibration and collision during transportation, resulting in leakage of 2-% pentanediate. Packaging materials should be resistant to corrosion of this compound and well sealed, such as suitable glass bottles, plastic bottles or metal containers, and tightly sealed.
    In addition, fire and explosion protection cannot be ignored. Ethyl 2-% pentanediate may be flammable. Fireworks should be strictly prohibited in storage and transportation areas, and fire-extinguishing equipment should be provided. Transportation vehicles must also comply with fire and explosion-proof regulations to ensure safety.
    Storage and transportation of 2-% pentanediate ethyl ester requires caution in terms of temperature, humidity, contact with sundries, packaging and fire and explosion protection, so as to ensure its quality and transportation and storage safety.