131980-62-6

Basic information

• Product Name: 8‐phenylindeno[1,2‐d]‐1,2,3‐dithiazole
• Synonyms: 8‐phenylindeno[1,2‐d]‐1,2,3‐dithiazole
• CAS NO: 131980-62-6
• Molecular Weight: 267.375
• Mol File: 131980-62-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 8‐phenylindeno[1,2‐d]‐1,2,3‐dithiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 8‐phenylindeno[1,2‐d]‐1,2,3‐dithiazole(131980-62-6)
• EPA Substance Registry System: 8‐phenylindeno[1,2‐d]‐1,2,3‐dithiazole(131980-62-6)

Safety Data

• Hazardous Substances Data: 131980-62-6(Hazardous Substances Data)

Upstream product

• 7282-69-1 3-phenyl-1-indanone oxime 
• 908093-98-1 diazodiphenylmethane 
• 131980-57-9 3,3-diphenyl-3H-pyrazolo<6,7-c>-1,3λ⁴δ²,5,2,4-trithiadiazepine 
• 131980-67-1 6-phenyl-10bH-indeno-<1,2-f>-1,3λ⁴δ²,5,2,4-trithiadiazepine 
• 146796-63-6 (E)-3-phenylindene 1-oxime 

Downstream Products

• 133414-24-1 8-phenylindeno<1,2-d>-1,2,3-dithiazole 2-oxide 

Relevant articles and documents

Fused 1,2,3-dithiazoles: Convenient synthesis, structural characterization, and electrochemical properties

A new general protocol for synthesis of fused 1,2,3-dithiazoles by the reaction of cyclic oximes with S2Cl2 and pyridine in acetonitrile has been developed. The target 1,2,3-dithiazoles fused with various carbocycles, such as indene,

Cyclopenta-1,2,3-dithiazoles and Related Compounds

Treatment of 3-phenylinden-1-one oxime 6 with disulfur dichloride gives the indenodithiazole 2 directly in 58percent; in the presence of Huenig's base the yield rises to 90percent.Indenone oxime 9 and indanone oxime 11 with disulfur dichloride both give t

Pyrazolotrithiadiazepines and their Unexpected Rearrangement to 1,2,3-Dithiazoles

Treatment of 6-bromotrithiadiazepine (1) with Huenig's base in the presence of diaryldiazomethanes (2) gives the trithiadiazepyne cycloadducts (3) which undergo a deep-seated thermal rearrangement to give fused 1,2,3-dithiazoles (4), for which a mechanism