7133-92-8

Basic information

• Product Name: Benzenecarbothioamide, 2-hydroxy-N-phenyl-
• CAS NO: 7133-92-8
• Molecular Formula: C13H11NOS
• Molecular Weight: 229.302
• Mol File: 7133-92-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenecarbothioamide, 2-hydroxy-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarbothioamide, 2-hydroxy-N-phenyl-(7133-92-8)
• EPA Substance Registry System: Benzenecarbothioamide, 2-hydroxy-N-phenyl-(7133-92-8)

Safety Data

• Hazardous Substances Data: 7133-92-8(Hazardous Substances Data)

Upstream product

• 75-15-0 carbon disulfide 
• 824-91-9 O-methoxymethylphenol 
• 103-72-0 phenyl isothiocyanate 
• 87-17-2 salicylanilide 

Downstream Products

• 7133-66-6 3-phenyl-benzo[e][1,3]oxazine-2,4-dithione 
• 1697-11-6 2,3-diphenyl-2H-1,3-benzoxazin-4(3H)-one 
• 20978-95-4 2-methyl-3-phenyl-2,3-dihydro-4H-1,3-benzoxazin-4-one 
• 104515-55-1 anhydro-3,5-diphenyl-4-hydroxy-2-(2-hydroxyphenyl)thiazolium hydroxide 
• 64402-65-9 2-methyl-3-phenyl-2,3-dihydro-benzo[e][1,3]oxazine-4-thione 
• 64402-66-0 2,3-diphenyl-2,3-dihydro-benzo[e][1,3]oxazine-4-thione 
• 7134-82-9 3-phenyl-4-thioxo-3,4-dihydro-benzo[e][1,3]oxazin-2-one 
• 104515-56-2 anhydro-2-(2-(cyclohexenyloxy)phenyl)-3,5-diphenyl-4-hydroxythiazolium hydroxide 
• 104515-59-5 anhydro-2-(2-((cyanomethyl)oxy)phenyl)-3,5-diphenyl-4-hydroxythiazolium hydroxide 
• 119298-08-7 anhydro-3,5-diphenyl-4-hydroxy-2-(2-(methacryloyloxy)phenyl)thiazolium hydroxide 
• 104515-57-3 C₂₇H₂₃NO₂S 
• 119298-15-6 C₂₅H₁₉NO₃S 
• 87-17-2 salicylanilide 

Relevant articles and documents

One-Pot Syntheses of Methyl p- and o-Hydroxydithiobenzoates from Phenol Ethers

Methyl p- and o-hydroxydithiobenzoates were prepared regiospecifically in a one-pot procedure from phenol methyl- and methoxymethyl,ethers, respectively.The p-hydroxy compounds were prepared by treatment of the methyl ethers with carbon disulfide, methyl iodide, and aluminum chloride.The second procedure involves ortho-metallation, carbon disulfide dithiocarboxylation, sulfur alkylation with methyl iodide, and in situ phenol deprotection with aluminum chloride/methyl iodide.

Studies on 2-hydroxythiobenzamide and 2-hydroxythiobenzanilide. 1. Synthesis of the compounds

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