Taiy Chemical
5-Chlorothiophene-2-carboxylic acid
Product Name 5-Chloro-2-thiophenecarboxylic acid
Synonyms:62668 5-Chlorothiophene-2-carboxylic acid; 5-chlorothiophene-2-carboxylate; 2-Thiophenecarboxylic acid, 5-chloro-; 2-Chlorothiophene-5-formicacid; 5-Chloro-2-thiophene carboxylic acid; 5-Chlorothiophene-2-carboxilic acid; 2-chlorothiophene-5-carboxylic acid
CAS RN. 24065-33-6
EINECS Add
Molecular Weight 161.5867
Molecular Formula C5H2ClO2S
Melting Point(℃) 146-150℃
Boiling Point(℃) 287°C at 760 mmHg
Flash Point(℃) 127.4°C
Hazard Symbols Xi Details
Xi
Risk Codes  R36/37/38;    Details
 R36/37/38;     Details
Safety Description  S26;S37/39;Details
 S26;S37/39; Details
FAQ
What is 5-Chlorothiophene-2-carboxylic acid and what are its uses?

5-Chlorothiophene-2-carboxylic acid is a chemical compound with a molecular formula C6H3ClO2S. It is used in various industries such as pharmaceuticals, agrochemicals, and materials science. This compound is often employed as a key intermediate in the synthesis of diverse organic compounds.

What are the advantages of using 5-Chlorothiophene-2-carboxylic acid in pharmaceutical applications?

5-Chlorothiophene-2-carboxylic acid is valued in pharmaceutical applications for its versatility in building complex molecular structures. It serves as a crucial building block in the synthesis of biologically active compounds, making it a valuable tool in drug discovery and development processes. Additionally, this compound exhibits favorable physicochemical properties that make it suitable for incorporation into drug molecules.

How is 5-Chlorothiophene-2-carboxylic acid utilized in agrochemical products?

In the field of agrochemistry, 5-Chlorothiophene-2-carboxylic acid plays a significant role in the production of pesticides, herbicides, and other agricultural chemicals. By serving as a precursor in the synthesis of active ingredients, this compound contributes to the development of effective crop protection products. Its reactive nature and compatibility with various chemical reactions make it a preferred choice for synthesizing agrochemicals.

What are the key characteristics of 5-Chlorothiophene-2-carboxylic acid that make it useful in materials science?

One of the key features of 5-Chlorothiophene-2-carboxylic acid that makes it valuable in materials science is its ability to participate in diverse chemical reactions. This allows for the customization of its chemical structure, leading to the creation of novel materials with specific properties. Its unique aromatic ring system and sulfur-containing functional groups enable the formation of polymers, coatings, and other advanced materials with tailored functionalities.

How can researchers and manufacturers access high-quality 5-Chlorothiophene-2-carboxylic acid for their applications?

To acquire premium-grade 5-Chlorothiophene-2-carboxylic acid for research, development, or production purposes, interested parties can contact reputable chemical suppliers or manufacturers. These suppliers offer reliable sources of the compound, ensuring its purity, consistency, and adherence to industry standards. By collaborating with established suppliers, researchers and manufacturers can access the necessary quantities of 5-Chlorothiophene-2-carboxylic acid to support their projects and applications.
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