structure of 4-(Cyclopropylsulfamoyl)benzene-1-sulfonyl chloride

4-(Cyclopropylsulfamoyl)benzene-1-sulfonyl chloride

CAS No.: 1000932-54-6
M. Wt: 295.8
M. Fa: C9H10ClNO4S2
InChI Key: IKRLTAZGFZYUGS-UHFFFAOYSA-N

Names and Identifiers of 1000932-54-6

CAS Number

1000932-54-6

EC Number

869-638-2

MDL Number

MFCD08899153

IUPAC Name

4-(cyclopropylsulfamoyl)benzenesulfonyl chloride

InChI

InChI=1S/C9H10ClNO4S2/c10-16(12,13)8-3-5-9(6-4-8)17(14,15)11-7-1-2-7/h3-7,11H,1-2H2

InChIKey

IKRLTAZGFZYUGS-UHFFFAOYSA-N

Canonical SMILES

C1CC1NS(=O)(=O)C2=CC=C(C=C2)S(=O)(=O)Cl

UNSPSC Code

12352100

Physical and chemical properties of 1000932-54-6

H Bond Acceptors

4

H Bond Donors

1

LogP

1.21482021633333

Molecular Formula

C9H10ClNO4S2

Molecular Weight

295.8

Safety Information of 1000932-54-6

Pictograms

Signal Word

 Danger

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000932-54-6

4-(Cyclopropylsulfamoyl)benzene-1-sulfonyl chloride has potential applications in various fields:

  • Medicinal Chemistry: As a precursor for synthesizing sulfonamide drugs, which are used in treating bacterial infections.
  • Chemical Synthesis: It serves as a reagent for introducing sulfonamide groups into organic molecules.
  • Research: Its unique structure makes it valuable for studying chemical reactivity and biological interactions in laboratory settings.

Interaction Studies of 1000932-54-6

Interaction studies involving 4-(cyclopropylsulfamoyl)benzene-1-sulfonyl chloride focus on its reactivity with biological molecules. Preliminary studies suggest that compounds with similar structures can interact with enzymes or receptors, potentially leading to inhibition of bacterial growth or modulation of biological pathways. Detailed interaction studies would be essential to fully understand its pharmacological potential and safety profile.