85193-07-3

Basic information

• Product Name: 1-S-methyl-1-S-phenyl-N-(5-chloroanthraquinon-1-yl)sulfoximide
• CAS NO: 85193-07-3
• Molecular Weight: 395.866
• Mol File: 85193-07-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-S-methyl-1-S-phenyl-N-(5-chloroanthraquinon-1-yl)sulfoximide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-S-methyl-1-S-phenyl-N-(5-chloroanthraquinon-1-yl)sulfoximide(85193-07-3)
• EPA Substance Registry System: 1-S-methyl-1-S-phenyl-N-(5-chloroanthraquinon-1-yl)sulfoximide(85193-07-3)

Safety Data

• Hazardous Substances Data: 85193-07-3(Hazardous Substances Data)

Upstream product

• 1193-82-4 racemic methyl phenyl sulfoxide 
• 85192-87-6 5-chloro-anthra<1,9-cd>isoxazol-6-one 
• 117-11-3 1-amino-5-chloroanthracene-9,10-dione 

Relevant articles and documents

Ring Opening Reactions of 6H-Anthraisoxazol-6-ones and Related Compounds

Nucleophilic attack of anthraisoxazol-6-ones, and of anthraisoxazole by various sulfoxides, triphenyl phosphine, and aliphatic or aromatic phosphites proceeded with cleavage of the nitrogen-oxygen bond of the isoxazole ring.This method provided ready access to substituted anthraquinones bearing sulfoximido-, triphenylphosphazo-, and dialkyl(aryl)phosphoramidic groups attached to the 1- and the 1,5-positions of the anthraquinone system.The structures of the newly synthesized anthraquinone derivatives were supported by analytical and spectral data. 1 -S,S-dimethyl-N-(5-benzamidoanthraquinon-1-yl)sulfoximide yielded in 90percent sulfuric acid the 1-amino-5-sulfoximido anthraquinone without hydrolyzing the sulfoximido group.