1094496-54-4

Basic information

• Product Name: N-[(1R,2R)-2-aMinocyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea
• Synonyms: N-[(1R,2R)-2-aMinocyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea;N-[(1R,2R)-2-Aminocyclohexyl]-N'-[[(1R,4aS,10aR)- 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-isopropyl - 1-phenanthrenyl]methyl]thiourea
• CAS NO: 1094496-54-4
• Molecular Weight: 441.71542
• Mol File: 1094496-54-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[(1R,2R)-2-aMinocyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(1R,2R)-2-aMinocyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea(1094496-54-4)
• EPA Substance Registry System: N-[(1R,2R)-2-aMinocyclohexyl]-N'-[[(1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-octahydro-1,4a-diMethyl-7-(1-Methylethyl)-1-phenanthrenyl]Methyl]-Thiourea(1094496-54-4)

Safety Data

• Hazardous Substances Data: 1094496-54-4(Hazardous Substances Data)

Upstream product

• 115269-93-7 (1R,4aS)-7-isopropyl-1-(isothiocyanatomethyl)-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene 
• 20439-47-8 (1R,2R)-1,2-diaminocyclohexane 

Downstream Products

• 1173373-71-1 1-((1R,2R)-2-(dimethylamino)cyclohexyl)-3-(((1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthren-1-yl)methyl)thiourea 

Relevant articles and documents

Highly enantioselective synthesis of γ-nitro heteroaromatic ketones in a doubly stereocontrolled manner catalyzed by bifunctional thiourea catalysts based on dehydroabietic amine: A doubly stereocontrolled approach to pyrrolidine carboxylic acids

A new class of dehydroabietic amine-substituted primary amine-thiourea bifunctional catalysts were designed and synthesized. The doubly stereocontrolled organocatalytic conjugate addition of a variety of heterocycles-bearing ketones to nitroalkenes was in