CAS 31491-45-9
:3-Furancarboxylic acid, 2-chloro-
Description:
3-Furancarboxylic acid, 2-chloro- is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing one oxygen atom. This compound features a carboxylic acid functional group (-COOH) and a chlorine substituent at the second position of the furan ring. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the carboxylic acid group imparts acidic properties, allowing it to participate in various chemical reactions, such as esterification and amidation. The chlorine atom can influence the compound's reactivity and polarity, making it useful in synthetic organic chemistry. Additionally, 3-furancarboxylic acid derivatives may exhibit biological activity, which can be of interest in pharmaceutical research. As with many chemical substances, safety precautions should be taken when handling this compound, as it may pose health risks or environmental hazards.
Formula:C5H3ClO3
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Found 3 products.
2-Chlorofuran-3-carboxylic acid
CAS:2-Chlorofuran-3-carboxylic acidFormula:C5H3ClO3Purity:97%Color and Shape: light brown powderMolecular weight:146.53g/mol2-chlorofuran-3-carboxylic acid
CAS:2-Chloro-3-carboxylic acid is a broad spectrum inhibitor of human herpesvirus 1 (HSV-1) and human herpesvirus 2 (HSV-2). It is a non-nucleoside inhibitor of DNA polymerases. The compound binds to the active site of the enzyme, preventing the formation of an active complex with the template strand. 2-Chloro-3-carboxylic acid inhibits both DNA polymerases and RNA polymerases. This antiviral drug has been shown to inhibit HSV replication in culture by 95%. 2C3CA has been shown to have high specificity for HSV type 1 and type 2, as well as for all other human DNA viruses, including adenoviruses and cytomegalovirus.
2C3CA is not active against other animal DNA viruses or bacterial DNA viruses.Formula:C5H3ClO3Purity:Min. 95%Molecular weight:146.53 g/mol


