1255215-29-2

Basic information

• Product Name: benzyl (S)-1-(4-chlorophenyl)-3-((1R,3R,5S)-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl)propylcarbamate
• Synonyms: benzyl (S)-1-(4-chlorophenyl)-3-((1R,3R,5S)-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl)propylcarbamate
• CAS NO: 1255215-29-2
• Molecular Weight: 536.117
• Mol File: 1255215-29-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl (S)-1-(4-chlorophenyl)-3-((1R,3R,5S)-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl)propylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl (S)-1-(4-chlorophenyl)-3-((1R,3R,5S)-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl)propylcarbamate(1255215-29-2)
• EPA Substance Registry System: benzyl (S)-1-(4-chlorophenyl)-3-((1R,3R,5S)-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl)propylcarbamate(1255215-29-2)

Safety Data

• Hazardous Substances Data: 1255215-29-2(Hazardous Substances Data)

Upstream product

• 1255215-23-6 (S)-benzyl 1-(4-chlorophenyl)-3-oxopropylcarbamate 
• 423165-08-6 exo-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octane p-toluenesulfonate 

Relevant articles and documents

Asymmetric synthesis of maraviroc (UK-427,857)

The asymmetric synthesis of Maraviroc (UK-427,857), a chemochine receptor 5 (CCR-5) receptor antagonist, based on an expeditious organocatalytic enantioselective assembly of the chiral βamino aldehyde key fragment is presented. The reactions were performed on a gram-scale and allow for the rapid construction of new Maraviroc analogues.