110228-59-6

Basic information

• Product Name: N-methyl-4-nitro-N-(phenylthio)benzenamine
• Synonyms: N-methyl-4-nitro-N-(phenylthio)benzenamine
• CAS NO: 110228-59-6
• Molecular Weight: 260.316
• Mol File: 110228-59-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-methyl-4-nitro-N-(phenylthio)benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyl-4-nitro-N-(phenylthio)benzenamine(110228-59-6)
• EPA Substance Registry System: N-methyl-4-nitro-N-(phenylthio)benzenamine(110228-59-6)

Safety Data

• Hazardous Substances Data: 110228-59-6(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 100-15-2 N-methyl(p-nitroaniline) 
• 931-59-9 benzenesulfenyl chloride 

Downstream Products

• 16003-14-8 2-phenylthiofuran 
• 110228-60-9 N-methyl-2-(phenylthio)-4-nitroaniline 
• 100-15-2 N-methyl(p-nitroaniline) 
• 882-33-7 diphenyldisulfane 
• 124251-74-7 (Z)-N-methyl-N-(4-nitrophenyl)-N'-<1-(phenylthio)hex-1-en-2-yl>acetamidine 
• 124251-67-8 (E)-N-methyl-N-(4-nitrophenyl)-N'-<1-(phenylthio)hex-1-en-2-yl>acetamidine 
• 124251-69-0 (E)-N-methyl-N-(4-nitrophenyl)-N'-<3-(phenylthio)but-2-en-2-yl>acetamidine 
• 124251-72-5 N-methyl-N-(4-nitrophenyl)-N'-<2-(phenylthio)-3,3-dimethylbut-1-enyl>acetamidine 
• 124251-77-0 (E)-N-methyl-N-(4-nitrophenyl)-N'-<1-(phenylthio)-3,3-dimethylbut-1-en-2-yl>acetamidine 
• 124251-71-4 (Z)-N-methyl-N-(4-nitrophenyl)-N'-<1-(phenylthio)-3,3-dimethylbut-1-en-2-yl>acetamidine 
• 124251-73-6 (Z)-N-methyl-N-(4-nitrophenyl)-N'-<1-(phenylthio)pent-1-en-2-yl>acetamidine 
• 124251-66-7 (E)-N-methyl-N-(4-nitrophenyl)-N'-<1-(phenylthio)pent-1-en-2-yl>acetamidine 
• 124251-70-3 (E)-N-methyl-N-(4-nitrophenyl)-N'-<4-(phenylthio)hex-3-en-3-yl>acetamidine 
• 1267983-83-4 1,3-dimethyl-5-nitro-3-(phenylthio)indolin-2-one 

Relevant articles and documents

Catalytic thia-Sommelet-Hauser rearrangement: Application to the synthesis of oxindoles

A series of 3-arylthio-1,3-disubstituted-oxindoles were prepared in good yields by the reaction of α-diazocarbonyl compounds and sulfenamides. The reaction involves a Rh-catalyzed thia-Sommelet-Hauser-type rearrangement.(Figure Presented)