CAS 13852-81-8

4-Chloro-2-nitrobenzenesulfonamide

Description:

4-Chloro-2-nitrobenzenesulfonamide, with the CAS number 13852-81-8, is an organic compound that features a sulfonamide functional group attached to a benzene ring, which is further substituted with both a chlorine atom and a nitro group. This compound typically appears as a solid and is characterized by its aromatic structure, which contributes to its chemical stability and reactivity. The presence of the sulfonamide group imparts specific properties, such as potential solubility in polar solvents and the ability to participate in various chemical reactions, including nucleophilic substitutions. The chlorine and nitro substituents enhance the compound's electrophilicity, making it useful in synthetic organic chemistry. Additionally, 4-Chloro-2-nitrobenzenesulfonamide may exhibit biological activity, which can be explored for pharmaceutical applications. Safety considerations should be taken into account, as compounds containing nitro and chloro groups can be hazardous and may require proper handling and disposal protocols.

Formula: C₆H₅ClN₂O₄S

InChI: InChI=1S/C6H5ClN2O4S/c7-4-1-2-6(14(8,12)13)5(3-4)9(10)11/h1-3H,(H2,8,12,13)

InChI key: InChIKey=QOQQUXGKXVOXTH-UHFFFAOYSA-N

SMILES: N(=O)(=O)C1=C(S(N)(=O)=O)C=CC(Cl)=C1

Synonyms:

• 2-Nitro-4-chlorobenzenesulfonamide
• 4-Chloro-2-Nitrobenzenesulfonamide
• Benzenesulfonamide, 4-chloro-2-nitro-
• NSC 81213
• Pnu 11958
• 4-Chloro-2-nitrobenzenesulphonamide

4-chloro-2-nitrobenzene-1-sulfonamide

CAS: 13852-81-8

Formula: C₆H₅ClN₂O₄S

Molecular weight: 236.6329

Ref: IN-DA0019DS

4-chloro-2-nitrobenzenesulfonamide, 98%

CAS: 13852-81-8

Formula: C₆H₅ClN₂O₄S

Purity: 95.0%

Molecular weight: 236.63

Ref: 10-F341035

4-chloro-2-nitrobenzenesulfonamide

CAS: 13852-81-8

4-Chloro-2-nitrobenzenesulfonamide is a sulfonamide that can inhibit the growth of bacteria. 4-Chloro-2-nitrobenzenesulfonamide has shown antibacterial activity against test organisms and has been shown to be active against staphylococcus in animal studies. It binds to the sulfaquinoxaline receptor on the bacterial cell surface, which prevents DNA synthesis and protein production. In addition, 4-chloro-2-nitrobenzenesulfonamide causes an antiproliferative effect on certain cancer cells by binding to ligands that are important for cell division. This chemical may have a ternary complex with metal ions such as nickel, zinc, or copper. However, further research into this area is required.

Formula: C₆H₅ClN₂O₄S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 236.63 g/mol

Ref: 3D-FC169705

Hydrochlorothiazide Impurity 16

CAS: 13852-81-8

Formula: C₆H₅ClN₂O₄S

Molecular weight: 236.63

Ref: ST-EA-CP-H3027