Atomfair Sodium benzenethiolate C6H5NaS CAS 930-69-8

Sodium Benzenethiolate (CAS No. 930-69-8) is a highly reactive organosulfur compound with the molecular formula C6H5NaS . This white to pale yellow crystalline powder is the sodium salt of benzenethiol (thiophenol) and is widely used as a nucleophile and strong base in organic synthesis. Its IUPAC name is sodium;benzenethiolate , and it is also known as Sodium thiophenoxide or Sodium phenylthiolate. With excellent solubility in polar solvents such as water, alcohols, and DMF, Sodium Benzenethiolate is a versatile reagent for the formation of thioethers, aryl sulfides, and other sulfur-containing compounds. It is particularly valuable in pharmaceutical intermediates, agrochemical synthesis, and…

Description

Sodium Benzenethiolate (CAS No. 930-69-8) is a highly reactive organosulfur compound with the molecular formula C6H5NaS. This white to pale yellow crystalline powder is the sodium salt of benzenethiol (thiophenol) and is widely used as a nucleophile and strong base in organic synthesis. Its IUPAC name is sodium;benzenethiolate, and it is also known as Sodium thiophenoxide or Sodium phenylthiolate. With excellent solubility in polar solvents such as water, alcohols, and DMF, Sodium Benzenethiolate is a versatile reagent for the formation of thioethers, aryl sulfides, and other sulfur-containing compounds. It is particularly valuable in pharmaceutical intermediates, agrochemical synthesis, and materials science research. Store in a cool, dry place under inert atmosphere to prevent decomposition.

Properties

  • CAS Number: 930-69-8
  • Complexity: 50.5
  • IUPAC Name: sodium;benzenethiolate
  • InChI: InChI=1S/C6H6S.Na/c7-6-4-2-1-3-5-6;/h1-5,7H;/q;+1/p-1
  • InChI Key: RZWQDAUIUBVCDD-UHFFFAOYSA-M
  • Exact Mass: 132.00096561
  • Molecular Formula: C6H5NaS
  • Molecular Weight: 132.16
  • SMILES: C1=CC=C(C=C1)[S-].[Na+]
  • Topological: 1
  • Monoisotopic Mass: 132.00096561
  • Physical Description: Faintly beige solid with a stench;
  • Synonyms: SODIUM BENZENETHIOLATE, 930-69-8, Sodium thiophenoxide, Sodium phenylthiolate, Benzenethiol, sodium salt, Sodium thiophenylate, Sodium phenylsulfide, Sodium phenylmercaptide, Thiophenyl sodium salt, UNII-75GF5O2O8Y, 75GF5O2O8Y, DTXSID1027342, HSDB 5771, Benzenethiol, sodium salt (1:1), EINECS 213-224-0, DTXCID307342, SODIUM BENZENETHIOLATE [HSDB], 213-224-0, sodium thiophenate, Sodium thiophenolate, sodium;benzenethiolate, Thiophenol sodium salt, Benzenethiol sodium salt, CAS-930-69-8, Sodium Benzenethiolate (technical grade, 90%), sodiothiobenzene, sodium benzenthiolate, sodium phenyl mercaptide, SCHEMBL425159, CHEMBL3182565, BCP14418, Tox21_201620, Tox21_303102, MFCD00066460, AKOS015833652, NCGC00257219-01, NCGC00259169-01, BP-30118, DB-057365, Sodium thiophenolate, technical grade, 90%, CS-0047716, NS00079964, Sodium thiophenolate, purum, >=96.5% (RT), Q27266385

Application

Sodium Benzenethiolate is widely employed as a nucleophilic reagent in organic synthesis for the preparation of thioethers and sulfides. It serves as a key intermediate in the pharmaceutical industry for the synthesis of sulfur-containing drug molecules. Researchers also utilize it in polymer chemistry to modify surfaces or create conductive materials. Additionally, it finds applications in agrochemical production for developing pesticides and herbicides.

Safety and Hazards

GHS Hazard Statements

  • H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]

Precautionary Statements

  • P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501

Hazard Classes and Categories

  • Skin Corr. 1B (100%)

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