108438-83-1

Basic information

• Product Name: N-(naphthalen-1-yl)-N-phenylbenzamide
• Synonyms: N-(naphthalen-1-yl)-N-phenylbenzamide
• CAS NO: 108438-83-1
• Molecular Weight: 323.394
• Mol File: 108438-83-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(naphthalen-1-yl)-N-phenylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(naphthalen-1-yl)-N-phenylbenzamide(108438-83-1)
• EPA Substance Registry System: N-(naphthalen-1-yl)-N-phenylbenzamide(108438-83-1)

Safety Data

• Hazardous Substances Data: 108438-83-1(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 634-42-4 N-1-naphthalenyl-benzamide 
• 1189-71-5 isocyanate de chlorosulfonyle 
• 108438-76-2 α,N-diphenyl-α-(1-naphthyl) nitrone 
• 90-30-2 N-phenyl-1-naphthylamine 
• 98-88-4 benzoyl chloride 

Relevant articles and documents

The Chapman rearrangement in a continuous-flow microreactor

The Chapman rearrangement is of practical significance in pharmaceutical and fine chemical industries. It is a high temperature reaction with an exothermic nature in numerous cases. The conventional batch-wise synthesis is limited by its operational compl

REARRANGEMENT OF NITRONES TO AMIDES USING CHLOROSULFONYL ISOCYANATE

Reaction of chlorosulfonyl isocyanate (CSI) with nitrones 1a-n and 5a,b has been studied. α,α,N-Triaryl nitrones 1a-n react with CSI to form the N,N-diaryl arylamides 3a-n and 4i-n in good yields.In the case of α-H,α,N-diaryl nitrones 5a,b however, two compounds viz., the rearranged product 11a,b and the 1,4-dihydro tetrazines 10a,b are formed.The effect of substituents on the rearrangement has been studied.It is found that the nature of the substituents has got a profound effect on the rearrangement.We have also noted that the rearrangement is independent of the syn or anti configurations of the nitrones.