794553-01-8

Basic information

• Product Name: 4-methyl-N-(4-oxo-3-phenoxy-1-phenyl-2-azetidinyl)-N-phenylbenzenesulfonamide
• Synonyms: 4-methyl-N-(4-oxo-3-phenoxy-1-phenyl-2-azetidinyl)-N-phenylbenzenesulfonamide
• CAS NO: 794553-01-8
• Molecular Formula: C28H24N2O4S
• Molecular Weight: 484.56616
• Mol File: 794553-01-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-methyl-N-(4-oxo-3-phenoxy-1-phenyl-2-azetidinyl)-N-phenylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N-(4-oxo-3-phenoxy-1-phenyl-2-azetidinyl)-N-phenylbenzenesulfonamide(794553-01-8)
• EPA Substance Registry System: 4-methyl-N-(4-oxo-3-phenoxy-1-phenyl-2-azetidinyl)-N-phenylbenzenesulfonamide(794553-01-8)

Safety Data

• Hazardous Substances Data: 794553-01-8(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 622-15-1 (E)-N,N'-diphenylformimidamide 
• 701-99-5 Phenoxyacetyl chloride 

Relevant articles and documents

Facile synthesis of 4-acylamino and 4-sulphonamido β-lactams

The cycloaddition reaction of trisubstituted amidines (7a-f) with acid chlorides in presence of triethylamine gave 4-acylamino and 4-sulphonamido-trans-β-lactams (9a-h) in very good yields. Similarly N,N'-diarylamidines (5a-d) on reaction with 2 equiv. of acid chlorides (8a,b) gave 4-acylamino-trans-β-lactams (10a-e) via in situ generated acylamidines followed by cycloaddition reaction. (C) 2000 Elsevier Science Ltd.