5 Chloro 2 Acetylthiophene
quinoline thiophene imidazole thiazole

5-Chloro-2-Acetylthiophene

Taiy Chemical

    Specifications

    HS Code

    466512

    Chemical Formula C6H5ClOS
    Molar Mass 162.62 g/mol
    Appearance Yellow to brown liquid
    Boiling Point 114 - 116 °C at 15 mmHg
    Density 1.326 g/cm³
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
    Flash Point 113 °C
    Pungent Odor Yes
    Cas Number 13679-64-6

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    General Information
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    Frequently Asked Questions

    As a leading 5-Chloro-2-Acetylthiophene 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 physical properties of 5-Chloro-2-Acetylthiophene?
    5-Chloro-2-acetylthiophene is one of the organic compounds. Its physical properties are quite impressive, let me tell you in detail.
    Looking at its appearance, it is often colorless to light yellow liquid, which is what it shows at room temperature and pressure. Its color is elegant and quite clear.
    When it comes to the boiling point, it is about 240-242 ° C. When the temperature rises gradually, this compound is like a phoenix nirvana, changing from liquid to gaseous state, and embarking on a different morphological journey. The value of the boiling point is actually a key indicator of its physical properties, which is related to its behavior in the thermal environment. < Br >
    Melting point is also an important physical parameter. The melting point of 5-chloro-2-acetylthiophene is about -20 ° C. When the temperature drops to this temperature, its molecular movement gradually slows down, from a disordered liquid state to an ordered solid state, like a sleeping spirit, waiting for the temperature to wake up.
    Furthermore, in terms of density, it is about 1.309 g/cm ³. This value reflects its mass per unit volume, which can help us understand the quality characteristics of its space occupation. In many practical application scenarios, this characteristic is very critical.
    Solubility cannot be ignored. It is soluble in common organic solvents such as ethanol, ether, etc. This solubility endows it with broad application prospects in organic synthesis and other fields, and can be blended with a variety of organic reagents to form new compounds.
    In addition, the physical properties such as vapor pressure and refractive index of 5-chloro-2-acetylthiophene also have a profound impact on its application in chemical and materials. Vapor pressure is related to its volatilization, and refractive index plays an important role in applications such as optical materials.
    All these physical properties are interrelated, and together outline the unique physical style of 5-chloro-2-acetylthiophene, laying a solid foundation for its application in scientific research and industrial production.
    What are the chemical properties of 5-Chloro-2-Acetylthiophene?
    5-Chloro-2-acetylthiophene is one of the organic compounds. It has many unique chemical properties.
    In this compound, the chlorine atom and acetyl group are connected to the thiophene ring, which has a unique structure and endows it with specific reactivity. The thiophene ring is inherently aromatic, but the introduction of chlorine atoms and acetyl groups changes the distribution of electron clouds and affects the overall chemical properties.
    From the perspective of reactivity, chlorine atoms have a certain nucleophilic substitution activity. Due to the large electronegativity of chlorine atoms and the strong polarity of carbon-chlorine bonds, they are easily attacked by nucleophiles, causing chlorine atoms to be replaced and new compounds to be formed. For example, when encountering nucleophiles such as hydroxyl anions, chlorine atoms may be replaced by hydroxyl groups to obtain derivatives containing hydroxyl groups.
    The presence of acetyl groups also plays an important role. Carbonyl is electrophilic and can undergo many reactions. If it can be added to nucleophiles, such as Grignard's reagent and the carbonyl reaction of 5-chloro-2-acetylthiophene, new carbon-carbon bonds can be formed, and complex compounds can be derived. And the α-hydrogen of the acetyl group has a certain acidity and can leave under the action of alkali, initiating reactions such as condensation.
    In addition, the aromatic nature of 5-chloro-2-acetylthiophene makes the molecule relatively stable. When participating in the reaction, it can maintain the basic framework of structure and provide a unique electronic environment for the reaction. Its diverse chemical properties make it widely used in the field of organic synthesis and can be used as an intermediate for the preparation of various compounds such as medicine, pesticides and functional materials.
    What are the main uses of 5-Chloro-2-Acetylthiophene?
    5-Chloro-2-acetylthiophene, this substance has a wide range of uses. In the field of medicine, it is a key intermediate for the synthesis of many special drugs. For example, when preparing drugs for the treatment of specific inflammation, it can be used as a starting material. After multiple steps of delicate chemical reactions, a molecular structure with precise pharmacological activity can be constructed, and the therapeutic effect can be exerted by the precise action on the targets of relevant inflammatory pathways.
    In the field of materials science, it plays an important role in the synthesis of organic optoelectronic materials. After ingenious chemical modification and polymerization, materials with unique optoelectronic properties can be prepared. Such materials show great potential in cutting-edge fields such as organic Light Emitting Diodes (OLEDs) and solar cells, which can improve the photoelectric conversion efficiency and stability of devices, and provide key assistance for technological innovation in related fields.
    Furthermore, in the fine chemical industry, 5-chloro-2-acetylthiophene is also an important raw material for the synthesis of high-end fragrances and special additives. In the synthesis of fragrances, it can endow fragrances with unique aroma characteristics and improve the sensory quality of products; in the synthesis of special additives, it can endow materials with excellent properties such as anti-oxidation and anti-corrosion, expanding the application scenarios and service life of materials.
    In summary, 5-chloro-2-acetylthiophene, with its diverse chemical properties and reactivity, plays an indispensable role in many important fields such as medicine, materials, and fine chemicals, and has made outstanding contributions to promoting technological progress and product upgrading in various fields.
    What are 5-Chloro-2-Acetylthiophene synthesis methods?
    The synthesis method of 5-chloro-2-acetylthiophene has been known for a long time. In the past, chemists in the field of organic synthesis worked hard to find a good way to prepare this compound.
    One method is to use thiophene as the base, first perform halogenation to introduce chlorine atoms. The halogenation process requires careful observation of the reaction conditions, such as temperature, reagent ratio, etc. With an appropriate halogenation reagent and a suitable solvent, control the temperature so that the chlorine atom precisely replaces the hydrogen atom at a specific position on the thiophene ring to obtain 5-chlorothiophene.
    Then, 5-chlorothiophene meets the acetylation reagent. The step of acetylation also has many key points. Choose a suitable acetylation reagent, such as acetyl chloride or acetic anhydride, etc. With the help of a catalyst, catalyze the acetylation reaction. The choice and amount of catalyst depend on the rate and yield of the reaction. In a specific reaction environment, the acetyl group is smoothly connected to the second position of 5-chlorothiophene, resulting in 5-chloro-2-acetylthiophene.
    Another way, or the thiophene can be acetylated first, and then halogenated. This change in order will also cause the reaction conditions to be different. When acetylating first, the general conditions of acetylation should also be carefully selected. During the subsequent halogenation, more attention should be paid to the positional selectivity of chlorine atom substitution, so that the reaction proceeds in the expected direction and finally achieves the purpose of synthesizing 5-chloro-2-acetylthiophene. Chemists have explored step by step in this synthesis process, continuously optimized the reaction conditions, and strived to improve the yield and simplify the operation, so as to make this synthesis method increasingly perfect.
    What are the precautions in storage and transportation of 5-Chloro-2-Acetylthiophene?
    5-Chloro-2-acetylthiophene is one of the organic compounds. During storage and transportation, many matters need to be carefully paid attention to.
    First of all, storage, this compound should be stored in a cool, dry and well-ventilated place. The cover is quite sensitive to temperature and humidity. If the environment is warm and humid, it may change its properties or even deteriorate. And it should be kept away from fires and heat sources to prevent the risk of fire, because it has certain flammability. The storage place must be separated from oxidants, acids, bases, etc. This is because its chemical properties are active, and contact with such substances can easily cause chemical reactions and damage its quality. At the same time, the storage container should be well sealed to avoid contact with the air to prevent oxidation and other reactions.
    As for transportation, the transportation vehicle should ensure that the vehicle is in good condition and has corresponding fire and emergency equipment. When loading and unloading, the operation must be gentle to prevent damage to the packaging container and material leakage. During transportation, the temperature and humidity should be closely monitored, and necessary temperature and humidity control measures should be taken according to the actual situation. In case of leakage, emergency measures should be taken immediately to evacuate personnel, isolate the contaminated area, carefully collect the leakage, and properly handle it in accordance with relevant regulations to avoid harm to the environment. In short, in the storage and transportation of 5-chloro-2-acetylthiophene, all details are related to safety and quality, and should not be ignored.