1256601-43-0

Basic information

• Product Name: tert-butyl (1R,2R)-2-(3-butynylamino)cyclohexylcarbamate
• Synonyms: tert-butyl (1R,2R)-2-(3-butynylamino)cyclohexylcarbamate
• CAS NO: 1256601-43-0
• Molecular Weight: 266.384
• Mol File: 1256601-43-0.mol

Chemical Properties

• CAS DataBase Reference: tert-butyl (1R,2R)-2-(3-butynylamino)cyclohexylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (1R,2R)-2-(3-butynylamino)cyclohexylcarbamate(1256601-43-0)
• EPA Substance Registry System: tert-butyl (1R,2R)-2-(3-butynylamino)cyclohexylcarbamate(1256601-43-0)

Safety Data

• Hazardous Substances Data: 1256601-43-0(Hazardous Substances Data)

Upstream product

• 23418-85-1 3-butyn-1-yl p-toluenesulfonate 
• 146504-07-6 tert-butyl ((1R,2R)-2-aminocyclohexyl)carbamate 

Downstream Products

• 1256601-45-2 1-(3,5-bis(trifluoromethyl)phenyl)-(1R,2R)-3-[2-(3-butynyl(methyl)amino)cyclohexyl]thiourea 
• 1256601-47-4 tert-butyl [(1R,2R)-2-[methyl[2-[1-[((R)-1-(2,2,2-trifluoroacetyl)pyrrolidin-2-yl)methyl]-1H-1,2,3-triazol-5-yl]ethyl]amino]cyclohexyl]carbamate 
• 1256601-49-6 tert-butyl (1R,2R)-2-((2-(1-(3-(cinnamoylcarbamoyl)benzyl)-1H-1,2,3-triazol-5-yl)ethyl)(methyl)amino)cyclohexylcarbamate 
• 1256601-50-9 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1R,2R)-2-(methyl(2-(1-((R)-pyrrolidin-2-ylmethyl)-1H-1,2,3-triazol-5-yl)ethyl)amino)cyclohexyl)thiourea 
• 1256601-44-1 tert-butyl (1R,2R)-2-(3-butynyl(methyl)amino)cyclohexylcarbamate 

Relevant articles and documents

Synthesis and properties of chiral thioureas bearing an additional function at a remote position tethered by a 1,5- disubstituted triazole

The synthesis and properties of multifunctional thioureas bearing a variety of functional groups at a position remote from the thiourea moiety are described. A 1, 5- disubstituted triazole tether connected with a thiourea and another functional group was synthesized via ruthenium catalyzed Huisgen cycloaddition. We demonstrate the utility of the synthetic thioureas as asymmetric catalysts and probes for the mechanistic elucidation of the course of the Michael reaction of an α,β-unsaturated imide.