CAS 728864-92-4

5-[(1-Oxopropyl)amino]-1-naphthalenesulfonyl chloride

Description:

5-[(1-Oxopropyl)amino]-1-naphthalenesulfonyl chloride, with the CAS number 728864-92-4, is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and ability to form sulfonamides. This compound features a naphthalene ring, which contributes to its aromatic properties and potential for π-π stacking interactions. The presence of the 1-oxopropylamino group indicates that it has an amine functionality, which can participate in nucleophilic reactions. The sulfonyl chloride moiety is particularly useful in organic synthesis, as it can react with various nucleophiles to form sulfonamides or other derivatives. This compound is likely to be a solid at room temperature and may exhibit moderate solubility in organic solvents. Due to its reactive nature, it should be handled with care, as sulfonyl chlorides can be corrosive and may release toxic gases upon hydrolysis. Overall, this compound is of interest in synthetic organic chemistry and may have applications in pharmaceuticals or agrochemicals.

Formula: C₁₃H₁₂ClNO₃S

InChI: InChI=1S/C13H12ClNO3S/c1-2-13(16)15-11-7-3-6-10-9(11)5-4-8-12(10)19(14,17)18/h3-8H,2H2,1H3,(H,15,16)

InChI key: InChIKey=RTKOSQNWLBWPSE-UHFFFAOYSA-N

SMILES: S(Cl)(=O)(=O)C=1C2=C(C(NC(CC)=O)=CC=C2)C=CC1

Synonyms:

• 5-[(1-Oxopropyl)amino]-1-naphthalenesulfonyl chloride
• 1-Naphthalenesulfonyl chloride, 5-[(1-oxopropyl)amino]-

5-Propionylamino-naphthalene-1-sulfonyl chloride

CAS: 728864-92-4

Formula: C₁₃H₁₂ClNO₃S

Color and Shape: Solid

Molecular weight: 297.75

Ref: 10-F020687