2 Thiophenecarbonyl Chloride 5 Chloro
quinoline thiophene imidazole thiazole

2-Thiophenecarbonyl chloride, 5-chloro-

Taiy Chemical

    Specifications

    HS Code

    149284

    Chemical Formula C5H2Cl2OS
    Molecular Weight 181.04
    Appearance Typically a liquid
    Odor Pungent odor
    Boiling Point Data may vary, around 220 - 230 °C
    Density Data needed from specific sources
    Solubility Soluble in common organic solvents like dichloromethane
    Reactivity Reactive towards nucleophiles, reacts with alcohols, amines
    Hazard Class Corrosive, can cause skin and eye irritation

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    General Information
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    Frequently Asked Questions

    As a leading 2-Thiophenecarbonyl chloride, 5-chloro- 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 chemical properties of 2-Thiophenecarbonyl chloride, 5-chloro-
    5-Chloro-2-thiophenoformyl chloride is an organic compound with unique chemical properties. Its appearance is often colorless to light yellow liquid, with a pungent smell and certain volatility.
    In terms of chemical activity, this substance is chemically active due to the presence of an acyl chloride group. In the acyl chloride group, the chlorine atom has strong electron absorption, resulting in a decrease in the electron cloud density of the carbonyl carbon atom, which is vulnerable to attack by nucleophiles, resulting in many nucleophilic substitution reactions. For example, when exposed to water, it is rapidly hydrolyzed to generate 5-chloro-2-thiophenoformic acid and hydrogen chloride. This hydrolysis reaction is violent and requires careful operation.
    In the presence of alcohols, alcoholysis reactions can occur to generate corresponding ester compounds. When interacted with amines, amides can be formed. These reactions are widely used in the field of organic synthesis, and can be used to construct various compounds containing thiophene structures for the preparation of drugs, pesticides and materials.
    Its solubility is generally soluble in common organic solvents, such as dichloromethane, chloroform, ether, etc., but it is difficult to dissolve in water. Due to its molecular structure, thiophene rings and acyl chloride groups are both hydrophobic parts, resulting in their overall solubility in water is extremely low. 5-Chloro-2-thiophenoformyl chloride plays an important role in the field of organic synthetic chemistry due to its active chemical properties and specific dissolution characteristics. However, due to its corrosive and irritating properties, safety procedures must be strictly followed when used.
    What are the main uses of 2-Thiophenecarbonyl chloride, 5-chloro-
    2-Thiophenoformyl chloride, 5-chlorine - This substance has a wide range of uses and is often used as a key intermediate in the field of organic synthesis. In the field of pharmaceutical creation, it can react with various amines and alcohols to construct structural units with specific biological activities, which can be used to develop new drugs, or to modify and optimize the structure of existing drugs to improve drug efficacy and reduce toxic and side effects. In the field of pesticides, it also plays an important role in the synthesis of many high-efficiency, low-toxicity and environmentally friendly pesticides, contributing to agricultural pest control and crop protection. In the field of materials science, it can be used as a raw material to synthesize organic materials with special photoelectric properties, such as functional materials used in organic Light Emitting Diodes (OLEDs), organic solar cells, etc., endowing materials with unique electrical and optical properties and improving device performance and efficiency. In short, 2-thiophenoformyl chloride, 5-chlorine - has great value in many chemical-related industries and scientific research fields, and is of great significance to promote the development of related industries.
    What is the preparation method of 2-Thiophenecarbonyl chloride, 5-chloro-?
    The method of making 5-chloro-2-thiophenoformyl chloride is an important task in organic synthesis. It can be achieved by several ways.
    First, 5-chloro-2-thiophenecarboxylic acid is used as the starting material. Co-place 5-chloro-2-thiophenecarboxylic acid with a chlorinated reagent in a suitable reaction vessel. Commonly used chlorinated reagents, such as thionyl chloride (SOCl ²), have good reactivity with acids. After the two are mixed, they are properly heated, usually between 50 and 80 degrees Celsius, heated and stirred. During this process, the chlorine atom of thionyl chloride replaces the hydroxyl group of the carboxyl group to generate 5-chloro-2-thiophenoformyl chloride, and at the same time escape sulfur dioxide and hydrogen chloride gas. After the reaction is completed, the excess thionyl chloride and other impurities are removed by reduced pressure distillation to obtain a pure product.
    Second, 5-chloro-2-thiophenaldehyde can also be used as a raw material. First, 5-chloro-2-thiophenylformaldehyde is oxidized to 5-chloro-2-thiophenylcarboxylic acid with an appropriate oxidizing agent, such as Jones reagent (a mixture of chromic acid and sulfuric acid). This oxidation reaction needs to control the temperature and the amount of reagents to prevent excessive oxidation. After obtaining 5-chloro-2-thiophenylcarboxylic acid, 5-chloro-2-thiophenylchloride is prepared by the above method of chlorination with thionyl chloride.
    Third, take 2-chloro-5-halothiophene as the starting material, and carry out carbonylation reaction with carbon monoxide and hydrogen chloride in a specific catalyst, such as palladium as the active component supported in the presence of a suitable carrier catalyst. This reaction needs to be carried out under certain pressure and temperature conditions, generally at 1-5 MPa, and the temperature is between 80-150 ° C. During the reaction, the halogen atom is replaced by a carbonyl group and a chlorine atom to form 5-chloro-2-thiophenoformyl chloride. After the reaction, the target product can be obtained through separation and purification steps, such as extraction, distillation, etc.
    All kinds of production methods have advantages and disadvantages. In practical application, the choice should be weighed according to factors such as raw material availability, cost, and product purity requirements.
    2-Thiophenecarbonyl chloride, 5-chloro - what are the precautions in storage and transportation
    2-Thiophenoformyl chloride, 5-chlorine, many matters must be paid attention to during storage and transportation. This is a chemical substance with specific chemical properties. When storing, the first choice of environment. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. The substance can easily cause danger due to heat, or cause unexpected decomposition or combustion.
    Furthermore, its packaging must be intact. Sealed packaging can effectively prevent it from contacting with air, moisture, etc. If the packaging is damaged, 5-chloro-2-thiophenoformyl chloride may react with components in the air, causing quality changes, and leakage will also pose a threat to the environment and personnel.
    When transporting, the selected means of transportation must be adapted. The relevant chemical transportation specifications should be followed to avoid mixing with oxidants, alkalis, etc. Due to its chemical activity, it can be mixed with other substances or react violently. The transportation process must be stable to prevent packaging damage caused by bumps.
    Operators also need to take protective measures. When storing and transporting, appropriate protective equipment should be worn, such as protective clothing, gloves, goggles, etc., to prevent the substance from contacting the skin and eyes and causing injury. In case of inadvertent contact, it should be disposed of quickly and properly according to the established emergency treatment procedures. In this way, the safety of storage and transportation can be guaranteed to avoid dangerous accidents.
    2-Thiophenecarbonyl chloride, 5-chloro - What are the effects on the environment and human health?
    2-Thiophenoformyl chloride, 5-chlorine - The impact of this substance on the environment and human health is not detailed in ancient books, but with today's scientific understanding, one or two insights can be gained.
    At the environmental end, 2-thiophenoformyl chloride, 5-chlorine - If these chemicals are accidentally released into nature, they may cause harm to aquatic ecosystems. It may dissolve into water bodies, and aquatic organisms bear the brunt. Such as fish, shellfish, etc., exposure to these substances may cause physiological disorders, stunted growth and development, and even endanger lives. And if this substance remains in the soil, or affects the activity of soil microorganisms, disrupts the ecological balance of the soil, causes damage to soil fertility, and affects plant growth.
    As for personal health, it is potentially harmful. If the human body ingests this substance through breathing, skin contact or accidental ingestion, there may be adverse consequences. Respiratory contact, or cause mucosal irritation, causing cough, asthma, etc.; skin contact, or cause allergies, burns, etc.; if accidentally ingested, it may hurt the stomach, cause nausea, vomiting, abdominal pain, etc., long-term or potential carcinogenic and teratogenic risks.
    Although "Tiangong Kaiwu" does not involve this specific substance, it is deduced from the ancient people's cognition of the influence of objects. All such chemically synthesized objects should be treated with caution to prevent them from escaping, so as to ensure environmental safety and human health. Make sure to strictly abide by the procedures during preparation and use, properly dispose of waste, and do not let them wantonly harm the world and people.