160193-58-8

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 125558-05-6 (1R,3S)-2,2-dimethyl-3-(2-oxopropyl)cyclopropanacetamide oxime 

Downstream Products

• 298201-64-6 Benzyl[(1R,3S)-2,2-dimethyl-3-(2-oxopropyl)cyclopropylmethyl]cyanamide 
• 298201-45-3 (2,6-Difluorobenzyl)-[(1R,3S)-2,2-dimethyl-3-(2-oxopropyl)cyclopropylmethyl]cyanamide 
• 298201-46-4 [(1R,3S)-2,2-Dimethyl-3-(2-oxopropyl)cyclopropylmethyl]pentafluorophenylmethylcyanamide 
• 160193-56-6 N-cyano-N-(m-phenoxybenzyl)<(1R,3S)-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropylmethyl>amine 
• 160193-60-2 N-cyano-N-(m-phenoxybenzyl)<(1R,3S)-2,2-dimethyl-3-(2-hydroxy-2-methylpropyl)cyclopropylmethyl>amine 
• 160193-59-9 N-cyano-N-(m-phenoxybenzyl)<(1R,3S)-2,2-dimethyl-3-(2-oxopropyl)cyclopropylmethyl>amine 

Relevant academic research and scientific papers

Modification of the Tiemann rearrangement: One-pot synthesis of N,N-disubstituted cyanamides from amidoximes

A three-stage one-pot synthetic procedure for transformation of amidoximes to N,N-disubstituted cyanamides in 70-92% yield is described.

Synthesis of an aza-analogue of pyrethroid cyphenothrin from (+)-3-carene

The preparation of N-cyano-N-(m-phenoxybenzyl)[(1R,3S)-2,2-dimethyl-3-(2-methyl-1 -propeny l)cyclopropylmethyl]amine (8) from monoterpene hydrocarbon (+)-3-carene is described.