125302-97-8

Basic information

• Product Name: N-Benzyl-N-cyclopropyl-3-chlorobenzamide
• CAS NO: 125302-97-8
• Molecular Weight: 285.773
• Mol File: 125302-97-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-Benzyl-N-cyclopropyl-3-chlorobenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzyl-N-cyclopropyl-3-chlorobenzamide(125302-97-8)
• EPA Substance Registry System: N-Benzyl-N-cyclopropyl-3-chlorobenzamide(125302-97-8)

Safety Data

• Hazardous Substances Data: 125302-97-8(Hazardous Substances Data)

Upstream product

• 13324-66-8 N-benzylcyclopropanamine 
• 618-46-2 m-Chlorobenzoyl chloride 

Relevant articles and documents

Amine-Induced Reactions of Diacyl Peroxides

The decompositions of 3-chlorobenzoyl cyclobutylformyl peroxide (3a), and 3-chlorobenzoyl cyclopropylacetyl peroxide (3b) induced by 1-azabicyclooctane (Q), N1,N1,N4,N4-tetramethyl-1,4-benzenediamine (W), 1,4-diazabicyclooctane (DABCO), and N,N-dimethylaniline (DMA) were investigated.Peroxides 3 were selected for study because distinctive product patterns were expected from decompositions induced by the alternative SN2 and SET pathways.Q and W were selected as amines likely to react by the SN2 and SET pathways, respectively.Q reacted with3 to give products characteristic of the intermediacy of an ion pair (general structure: R3NOCOC4H7+ArCO2-) formed by the SN2 pathway, while W reacted with 3 to give rapid formation of the C4H7CO2 radical, indicative of an SET pathway.Based on the results with Q and W, we interpret the results with DABCO and DMA to indicate that both induce the decomposition of 3 by the SN2 pathway.Thus, peroxides 3 have been shown to be structurally sensitive to the modes of their induced decomposition, and are, potentially, mechanistic probes for ascertaining the mechanism of induced peroxide decomposition by closed-shell molecules.