32306-42-6

Basic information

• Product Name: 2(3H)-Thiazolethione, 3,4-diphenyl-
• CAS NO: 32306-42-6
• Molecular Formula: C15H11NS2
• Molecular Weight: 269.391
• Mol File: 32306-42-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2(3H)-Thiazolethione, 3,4-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Thiazolethione, 3,4-diphenyl-(32306-42-6)
• EPA Substance Registry System: 2(3H)-Thiazolethione, 3,4-diphenyl-(32306-42-6)

Safety Data

• Hazardous Substances Data: 32306-42-6(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 98-86-2 acetophenone 
• 7257-94-5 1-phenyl-2-(p-tolylsulfonyloxy)ethanone 
• 1074-52-8 ammonium phenyldithiocarbamate 
• 70-11-1 α-bromoacetophenone 
• 75-15-0 carbon disulfide 
• 43009-16-1 phenyldithiocarbamic acid triethylamine salt 

Downstream Products

• 69809-56-9 2-(3,4-diphenyl-3H-thiazol-2-ylidene)-1-phenyl-ethanethione 
• 69809-67-2 6-(3,4-diphenyl-3H-thiazol-2-ylidenemethyl)-6-phenyl-6H-thiopyran-2,3,4,5-tetracarboxylic acid tetramethyl ester 
• 42047-02-9 benzoic acid-(3,4-diphenyl-3H-thiazol-2-ylidenehydrazide) 
• 110152-93-7 (Z)-3,4-diphenyl-2-(propan-2-ylidenehydrazono)-2,3-dihydrothiazole 
• 54809-89-1 (3-amino-4-phenyl-3H-thiazol-2-ylidene)-phenyl-amine 
• 69809-53-6 2-(3,4-diphenyl-3H-thiazol-2-ylidene)-1-phenyl-ethanone 
• 15995-39-8 3,4-diphenyl-3H-thiazol-2-one dimethylhydrazone 

Relevant articles and documents

4,5-Substituted ?C? cyclometalated thiazol-2-ylidene platinum(II) complexes-synthesis and photophysical properties

We report the synthesis of seven novel backbone functionalized N-phenyl-1,3-thiazol-2-ylidene platinum(ii) complexes and their photophysical properties. Electronically diverse N-phenyl-1,3-thiazol-2-thiones were prepared by a reaction of aniline with carb

A facile synthesis of thiazole-2(3H)-thiones through [hydroxy(tosyloxy) iodo]benzene

A one-pot facile synthesis of thiazole-2(3H)-thiones (4) has been achieved by hypervalent iodine oxidation of ketones (1) using [hydroxy (tosyloxy)iodo]benzene, followed by the treatment of the reaction mixture with dithiocarbamate salts (3) The intermediate α-tosyloxy-ketones (2) have also been isolated and converted to the target compounds.