73726-60-0

Basic information

• Product Name: 2-hydroxythiophenol diacetic ester
• Synonyms: 2-hydroxythiophenol diacetic ester
• CAS NO: 73726-60-0
• Molecular Weight: 210.254
• Mol File: 73726-60-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-hydroxythiophenol diacetic ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hydroxythiophenol diacetic ester(73726-60-0)
• EPA Substance Registry System: 2-hydroxythiophenol diacetic ester(73726-60-0)

Safety Data

• Hazardous Substances Data: 73726-60-0(Hazardous Substances Data)

Upstream product

• 82766-15-2 2-ethyl-2-methyl-benz[1,3]oxathiol 
• 75-36-5 acetyl chloride 
• 1113062-66-0 C₄₂H₃₄OSSn₂ 
• 108-24-7 acetic anhydride 
• 54226-25-4 2,2-diethyl-benzo[1,3]oxathiole 
• 274-26-0 1,3-benzoxathiole 
• 29026-66-2 spiro<1,3-benzoxathiole-2,1'-cyclohexane> 
• 29026-64-0 2-methyl-2-propyl-benzo[1,3]oxathiole 
• 29026-65-1 spiro<1,3-benzoxathiole-2,1'-cyclopentane> 
• 1121-24-0 ortho-mercaptophenol 
• 61329-21-3 2-chloro-1,,3,2-benzoxathiastibole 
• 92608-05-4 2-methyl-2-isopropyl-1,3-benzoxathiole 
• 7740-07-0 2,2-dimethylbenzo[d][1,3]oxathiole 
• 39961-89-2 2-chloro-1,3,2-benzo-oxathia-arsole 

Relevant articles and documents

A new strategy for chemoselective O-acylation of β-mercapto alcohols via alkylsilyl and stannyl protection

Chemoselective preparation of O-acylated derivatives from bis-protected mercapto alcohols was described. Trialkylsilyl and trialkylstannyl chloride are used to generate an intermediate with O- and S-protection. The intermediates from β-mercapto alcohols a

On the Acylation of 1,3-Benzoxathiole Systems

The acylation on 1,3-benzoxathiole systems, as well as the effect of the stoichiometry of the catalyst on the yields of ketones and of breaking products of the O-C-S bonds is here described.

Studies on the Synthesis of Heterocyclic Compounds. VIII. Action of Acyl Halides on 2,2-di-n-butyl-1,3,2-benzoxathiastannole, 2-Chloro-1,3,2-benzoxathiaarsole and -stibole

The cleavage reaction of some 1,3,2-benzoxathiastannole,-arsole and -stibole derivatives with acetyl and benzoyl chloride is described.The reactions were carried out refluxing in benzene or at room temperature.In all cases, the reaction occurs through the initial cleavage of the S-M linkage with formation of the respective o-acylthio derivatives.The structure of the prepared compounds was assigned on the basis of their analytical, physical and spectral data.