17570-85-3

Basic information

• Product Name: N-benzoyl-N-thiobenzoyl-aniline
• Synonyms: N-benzoyl-N-thiobenzoyl-aniline
• CAS NO: 17570-85-3
• Molecular Weight: 317.411
• Mol File: 17570-85-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-benzoyl-N-thiobenzoyl-aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzoyl-N-thiobenzoyl-aniline(17570-85-3)
• EPA Substance Registry System: N-benzoyl-N-thiobenzoyl-aniline(17570-85-3)

Safety Data

• Hazardous Substances Data: 17570-85-3(Hazardous Substances Data)

Upstream product

• 71-23-8 propan-1-ol 
• 18100-80-6 2,3,5-triphenyl-4-thiazolone 
• 67-66-3 chloroform 
• 98-88-4 benzoyl chloride 
• 636-04-4 N-Phenylbenzothioamide 
• 103841-78-7 N-isobutyroyl-N-phenylthiobenzamide 
• 64-17-5 ethanol 
• 67-56-1 methanol 
• 28170-13-0 thiobenzoic acid potassium salt 
• 4903-36-0 N-phenyl-benzimidoyl chloride 

Downstream Products

• 65-85-0 benzoic acid 
• 636-04-4 N-Phenylbenzothioamide 
• 93-58-3 benzoic acid methyl ester 
• 98-88-4 benzoyl chloride 

Relevant articles and documents

N-phenyl-N-(phenylthioxomethyl)benzamide

The title molecule, C20H15NOS, adopts an (ES,ZO) conformation, similar to that of other monothioimides, with an intramolecular O...-C(S) contact of 2.821 (5) A; a photochemical cleavage reaction probably proceeds via intramolecular nucleophilic attack of oxygen on the C=S double bond in the presence of solvolytic agents.

CARBONSAEURE-IMIDSAEURE-THIOANHYDRIDE AUS THIOAMIDEN UND CARBONSAEURECHLORIDEN IM ZWEIPHASENSYSTEM FLUESSIG-FEST

By acylation of thioamides in a two phase system liquid-solid with acetone-NaOH the hitherto unknown S-acylderivatives of the thioamides are obtained which may be regarded as Carboxylic acid-imidic acid-thioanhydrides.Some compounds of the new class can b

Reaction of Mesoionic Thiazolones with m-Chloroperbenzoic Acid. Oxidative Dipole Extensions

The oxidation of anhydro-4-hydroxy-2,3,5-triarylthiazolium hydroxides (1) with m-chloroperbenzoic acid gave (in primary alcohols) 2,5-dialkoxy-2,3,5-triarylthiazolidin-4-ones (5) and N-aroylthiobenzanilides (6).Oxidation of anhydro-5-hydroxy-3-methyl-2-phenylthiazolium hydroxide (2) gave 3-methyl-2-phenylthiazolidine-4,5-dione (8) and N-formyl-N-methylthiobenzamide (9).The products arise from initial oxidations at the carbon atoms at position 5 of 1 and position 4 of 2, and transformation modes to the final products are discussed.These oxidations are the first examples of oxidative dipole extensions.