CAS 89665-79-2

1-(2-chlorophenyl)methanesulfonamide

Description:

1-(2-Chlorophenyl)methanesulfonamide is an organic compound characterized by the presence of a sulfonamide functional group attached to a methanesulfonyl moiety and a 2-chlorophenyl group. This compound typically appears as a solid at room temperature and is soluble in polar solvents due to the sulfonamide group, which can engage in hydrogen bonding. The presence of the chlorine atom on the phenyl ring can influence the compound's reactivity and biological activity, often enhancing its lipophilicity and altering its electronic properties. This compound may exhibit various pharmacological activities, making it of interest in medicinal chemistry. Its sulfonamide structure is known for its role in various therapeutic agents, particularly as antibiotics and diuretics. Safety data should be consulted for handling and potential toxicity, as sulfonamides can cause allergic reactions in some individuals. Overall, 1-(2-chlorophenyl)methanesulfonamide is a compound of interest in both synthetic and medicinal chemistry contexts.

Formula: C₇H₈ClNO₂S

InChI: InChI=1/C7H8ClNO2S/c8-7-4-2-1-3-6(7)5-12(9,10)11/h1-4H,5H2,(H2,9,10,11)

SMILES: c1ccc(c(c1)CS(=O)(=O)N)Cl

Synonyms:

• Benzenemethanesulfonamide, 2-Chloro-

Benzenemethanesulfonamide, 2-chloro-

CAS: 89665-79-2

Formula: C₇H₈ClNO₂S

Purity: %

Color and Shape: Solid

Molecular weight: 205.6619

Ref: IN-DA00H2QN

(2-Chlorophenyl)methanesulfonamide

CAS: 89665-79-2

(2-Chlorophenyl)methanesulfonamide

Purity: 95+%

Molecular weight: 205.67g/mol

Ref: 54-OR1034976

(2-CHLOROPHENYL)METHANESULFONAMIDE

CAS: 89665-79-2

Formula: C₇H₈ClNO₂S

Purity: 95+%

Color and Shape: Solid

Molecular weight: 205.66

Ref: 10-F468845

2-Chlorobenzylsulfonamide

CAS: 89665-79-2

2-Chlorobenzylsulfonamide is a drug that binds to the receptor for neutral lipids, which is found on the surface of human fibroblasts. This binding inhibits the release of free fatty acids from adipose tissue and also prevents the uptake of these lipids by tissues such as muscle. 2-Chlorobenzylsulfonamide has been shown to be effective at reducing hyperlipidemia in mice. This drug has a limited effect on heparin-induced lipoprotein lipase activity in vivo, but it does have an antidiabetic effect on rats when given orally. The mechanism of this effect may be due to its ability to inhibit lipolysis or to activate lipoprotein lipase.

Formula: C₇H₈ClNO₂S

Purity: Min. 95%

Molecular weight: 205.66 g/mol

Ref: 3D-PDA66579