Atomfair

Awaiting product image

Atomfair 2-Chlorobenzyl mercaptan C7H7ClS

Description 2-Chlorobenzyl mercaptan (CAS No. 17733-22-1), also known as (2-chlorophenyl)methanethiol, is a high-purity organosulfur compound with the molecular formula C7H7ClS . This specialized chemical features a chlorinated benzyl group bonded to a thiol (-SH) functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 158.65 g/mol, it is supplied as a clear to pale yellow liquid with a characteristic sulfurous odor. Our product undergoes rigorous QC testing including GC-MS and NMR to ensure ??98% purity, ideal for demanding applications in medicinal chemistry, ligand design, and materials science. Proper storage under inert atmosphere…

Category:
Brands:

Description

Description

2-Chlorobenzyl mercaptan (CAS No. 17733-22-1), also known as (2-chlorophenyl)methanethiol, is a high-purity organosulfur compound with the molecular formula C7H7ClS. This specialized chemical features a chlorinated benzyl group bonded to a thiol (-SH) functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 158.65 g/mol, it is supplied as a clear to pale yellow liquid with a characteristic sulfurous odor. Our product undergoes rigorous QC testing including GC-MS and NMR to ensure ??98% purity, ideal for demanding applications in medicinal chemistry, ligand design, and materials science. Proper storage under inert atmosphere at 2-8??C is recommended to prevent oxidation.

  • CAS No: 17733-22-1
  • Molecular Formula: C7H7ClS
  • Molecular Weight: 158.65
  • Exact Mass: 157.9956991
  • Monoisotopic Mass: 157.9956991
  • IUPAC Name: (2-chlorophenyl)methanethiol
  • SMILES: C1=CC=C(C(=C1)CS)Cl
  • Synonyms: 2-Chlorobenzyl mercaptan, 39718-00-8, 2-Chlorobenzenemethanethiol, (2-Chlorophenyl)methanethiol, 2-Chlorobenzylmercaptan

Application

2-Chlorobenzyl mercaptan serves as a versatile building block in pharmaceutical synthesis, particularly for creating sulfur-containing heterocycles. Researchers utilize it as a thiolating agent in nucleophilic substitution reactions to introduce the -SCH2(2-Cl-C6H4) moiety. The compound finds application in catalytic systems as a ligand precursor for transition metal complexes. In materials science, it functions as a surface modifier for gold nanoparticles due to its thiol-gold affinity.

If you are interested or have any questions, please contact us at support@atomfair.com