313959-45-4

Basic information

• Product Name: N-(2-benzoyl-4-methylphenyl)-2-nitrobenzenesulfonamide
• Synonyms: N-(2-benzoyl-4-methylphenyl)-2-nitrobenzenesulfonamide
• CAS NO: 313959-45-4
• Molecular Weight: 396.423
• Mol File: 313959-45-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(2-benzoyl-4-methylphenyl)-2-nitrobenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-benzoyl-4-methylphenyl)-2-nitrobenzenesulfonamide(313959-45-4)
• EPA Substance Registry System: N-(2-benzoyl-4-methylphenyl)-2-nitrobenzenesulfonamide(313959-45-4)

Safety Data

• Hazardous Substances Data: 313959-45-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 106-49-0 p-toluidine 
• 17852-28-7 2-amino-5-methylbenzophenone 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 

Downstream Products

• 88312-94-1 2-amino-N-(2-benzoyl-4-methylphenyl)benzenesulfonamide 

Relevant articles and documents

HETEROCYCLIC SYNTHESES VIA CARBANIONICALLY INDUCED REARRANGEMENT REACTIONS

The easily occuring -migrations of sulfonyl and carbonyl functions to neighboring phenyl anions can be utilized for ring expansions by one benzo unit when suitably tailored precursor heterocycles are used.Thus, the 1,2- benzisothiazol dioxide systems 8 and 17 can be transformed into dibenzothiazepin dioxides 12 and 21, respectively, whereas the dibenzo- and 1,2,4-benzothiazin dioxide models 35 and 46 give rise to the tribenzothiazocin dioxide and dibenzothiadiazocin dioxide systems 38 and 47, respectively.Unexpected formations of heterocyclic systems, namely, spirobenzoxazin-5,1'(3H)-isobenzofuran> 55, 3,1-benzoxazin 62, and phenanthridinium-salt 70 took place when phtalimide 52, dibenzoylaniline 56, and biphenylylbenzamide 65 were reacted with t-BuLi.