934420-94-7

Basic information

• Product Name: N-[(3-bromo-phenyl)-butylcarbamoyl-methyl]-N-(2-hydroxy-ethyl)-2-(toluene-4-sulfonylamino)-benzamide
• Synonyms: N-[(3-bromo-phenyl)-butylcarbamoyl-methyl]-N-(2-hydroxy-ethyl)-2-(toluene-4-sulfonylamino)-benzamide
• CAS NO: 934420-94-7
• Molecular Weight: 602.549
• Mol File: 934420-94-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[(3-bromo-phenyl)-butylcarbamoyl-methyl]-N-(2-hydroxy-ethyl)-2-(toluene-4-sulfonylamino)-benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(3-bromo-phenyl)-butylcarbamoyl-methyl]-N-(2-hydroxy-ethyl)-2-(toluene-4-sulfonylamino)-benzamide(934420-94-7)
• EPA Substance Registry System: N-[(3-bromo-phenyl)-butylcarbamoyl-methyl]-N-(2-hydroxy-ethyl)-2-(toluene-4-sulfonylamino)-benzamide(934420-94-7)

Safety Data

• Hazardous Substances Data: 934420-94-7(Hazardous Substances Data)

Upstream product

• 3132-99-8 m-bromobenzoic aldehyde 
• 2769-64-4 n-butyl isonitrile 
• 6311-23-5 2-(toluene-4-sulfonylamino)-benzoic acid 

Relevant articles and documents

Ugi multicomponent reaction followed by an intramolecular nucleophilic substitution: Convergent multicomponent synthesis of 1-sulfonyl 1,4-diazepan-5-ones and of their benzo-fused derivatives

A short, two-step approach to the synthesis of diazepane or diazocane systems, based on a Ugi multicomponent reaction followed by a subsequent intramolecular SN2 reaction was studied. 1 -Sulfonyl tetrahydrobenzo[e]-1,4-diazepin-1-ones 1 were ob