140903-52-2

Basic information

• Product Name: (2S,3R,4S)-2-<carbonyl>-3-(4-thiazoyl)-L-alanyl>amino>-1-cyclohexyl-3,4-dihydroxy-6-methylheptane
• Synonyms: (2S,3R,4S)-2-<carbonyl>-3-(4-thiazoyl)-L-alanyl>amino>-1-cyclohexyl-3,4-dihydroxy-6-methylheptane
• CAS NO: 140903-52-2
• Molecular Weight: 654.871
• Mol File: 140903-52-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3R,4S)-2-<carbonyl>-3-(4-thiazoyl)-L-alanyl>amino>-1-cyclohexyl-3,4-dihydroxy-6-methylheptane(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,4S)-2-<carbonyl>-3-(4-thiazoyl)-L-alanyl>amino>-1-cyclohexyl-3,4-dihydroxy-6-methylheptane(140903-52-2)
• EPA Substance Registry System: (2S,3R,4S)-2-<carbonyl>-3-(4-thiazoyl)-L-alanyl>amino>-1-cyclohexyl-3,4-dihydroxy-6-methylheptane(140903-52-2)

Safety Data

• Hazardous Substances Data: 140903-52-2(Hazardous Substances Data)

Upstream product

• 141042-62-8 <1R-(1α,2β,3α)>-1-(4-morpholinylcarbonyl)-3-phenylcyclopropane-2-carboxaldehyde 
• 140926-05-2 <1R-(1α,2α,3α)>-1-(4-morpholinylcarbonyl)-3-phenylcyclopropane-2-carboxaldehyde 
• 141041-95-4 <1R-(1α,2α,3α)>-2-(hydroxymethyl)-1-(4-morpholinylcarbonyl)-3-phenylcyclopropane 
• 136010-42-9 N-(tert-butoxycarbonyl)-4-thiazolylalaninyl amide of (2S,3R,4S)-2-amino-1-cyclohexyl-3,4-dihydroxy-6-methylheptane 
• 132435-60-0 (1R-(1α,5α,6α))-6-phenyl-3-oxabicyclo[3.1.0]hexan-2-one 
• 119434-75-2 (S)-3-(4-thiazolyl)-2-tert-butoxycarbonylaminopropanoic acid 
• 104882-10-2 (2S,3R,4S)-2-[(tert-butyloxycarbonyl)amino]-1-cyclohexyl-3,4-dihydroxy-6-methylheptane 
• 122621-77-6 (2S,3R,4S)-2-amino-1-cyclohexyl-3,4-dihydroxy-6-methylheptane 
• 136010-43-0 (2S,3R,4S)-2-<(L-4-thiazolylalanyl)amino>-1-cyclohexyl-3,4-dihydroxy-6-methylheptane 
• 141042-69-5 <1R-(1α,2β,3β)>-2-(4-morpholinylcarbonyl)-3-phenylcyclopropanecarboxylic acid 

Relevant articles and documents

1,2,3-Trisubstituted Cyclopropanes as Conformationally Restricted Peptide Isosteres: Application to the Design and Synthesis of Novel Renin Inhibitors

The 1,2,3-trisubstituted cyclopropanes 6 and 7 are the first members of a novel class of isosteric replacements for peptide linkages that are more generally represented by the dipeptide mimics 2 and 3.These unique peptide surrogates are specifically desig