CAS 728864-81-1

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

Description:

5-[(1-Piperidinylcarbonyl)amino]-1-naphthalenesulfonyl chloride, with the CAS number 728864-81-1, 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 piperidinylcarbonyl group indicates that it has a piperidine moiety, which can enhance its solubility and biological activity. As a sulfonyl chloride, it is likely to be sensitive to moisture and can react with nucleophiles, making it useful in organic synthesis, particularly in the formation of sulfonamides and other derivatives. The compound may exhibit biological activity, potentially serving as a pharmacophore in medicinal chemistry. However, due to the presence of the sulfonyl chloride group, it should be handled with care, as it can be corrosive and may release hydrochloric acid upon hydrolysis.

Formula: C₁₆H₁₇ClN₂O₃S

InChI: InChI=1S/C16H17ClN2O3S/c17-23(21,22)15-9-5-6-12-13(15)7-4-8-14(12)18-16(20)19-10-2-1-3-11-19/h4-9H,1-3,10-11H2,(H,18,20)

InChI key: InChIKey=VUCCZJWWIKLNPQ-UHFFFAOYSA-N

SMILES: N(C(=O)N1CCCCC1)C=2C3=C(C(S(Cl)(=O)=O)=CC=C3)C=CC2

Synonyms:

• 1-Naphthalenesulfonyl chloride, 5-[(1-piperidinylcarbonyl)amino]-
• 5-[(1-Piperidinylcarbonyl)amino]-1-naphthalenesulfonyl chloride
• 5-(Piperidine-1-carboxamido)naphthalene-1-sulfonyl chloride
• 5-[(PIPERIDINE-1-CARBONYL)-AMINO]-NAPHTHALENE-1-SULFONYL CHLORIDE