Methyl 5-(chlorosulfonyl)furan-2-carboxylate is a chemical compound characterized by its furan ring structure, which is a five-membered aromatic ring containing one oxygen atom. This compound features a chlorosulfonyl group, which is a sulfonyl group (–SO2) with a chlorine atom attached, contributing to its reactivity and potential applications in organic synthesis. The presence of the methyl ester group (–COOCH3) indicates that it can undergo hydrolysis to yield the corresponding carboxylic acid. The chlorosulfonyl moiety enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions. This compound is typically handled with care due to its potential reactivity and the presence of chlorine, which can pose health hazards. It is often utilized in the synthesis of more complex organic molecules, particularly in pharmaceutical and agrochemical research. As with many sulfonyl compounds, it may exhibit properties such as solubility in polar solvents and stability under specific conditions, but it is essential to consult safety data sheets for handling and storage guidelines.

methyl 5-(chlorosulfonyl)furan-2-carboxylate

69816-05-3: Methyl 5-(chlorosulfonyl)furan-2-carboxylate is a chemical compound characterized by its furan ring structure, which is a five-membered aromatic ring containing one oxygen atom. This compound features a chlorosulfonyl group, which is a sulfonyl group (–SO2) with a chlorine atom attached, contributing to its reactivity and potential applications in organic synthesis. The presence of the methyl ester group (–COOCH3) indicates that it can undergo hydrolysis to yield the corresponding carboxylic acid. The chlorosulfonyl moiety enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions. This compound is typically handled with care due to its potential reactivity and the presence of chlorine, which can pose health hazards. It is often utilized in the synthesis of more complex organic molecules, particularly in pharmaceutical and agrochemical research. As with many sulfonyl compounds, it may exhibit properties such as solubility in polar solvents and stability under specific conditions, but it is essential to consult safety data sheets for handling and storage guidelines.

CAS 69816-05-3

methyl 5-(chlorosulfonyl)furan-2-carboxylate

Methyl 5-(chlorosulfonyl)furan-2-carboxylate

Ref: IN-DA005TM4

Methyl 5-(chlorosulphonyl)-2-furoate

Ref: 54-OR8120

Methyl 5-(chlorosulfonyl)-2-furoate

Ref: 10-F017043