866395-22-4

Basic information

• Product Name: (S)-N-(benzyloxycarbonyl)-3-amino-4-methylpentan-1-ol
• Synonyms: (S)-N-(benzyloxycarbonyl)-3-amino-4-methylpentan-1-ol
• CAS NO: 866395-22-4
• Molecular Weight: 251.326
• Mol File: 866395-22-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-N-(benzyloxycarbonyl)-3-amino-4-methylpentan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-(benzyloxycarbonyl)-3-amino-4-methylpentan-1-ol(866395-22-4)
• EPA Substance Registry System: (S)-N-(benzyloxycarbonyl)-3-amino-4-methylpentan-1-ol(866395-22-4)

Safety Data

• Hazardous Substances Data: 866395-22-4(Hazardous Substances Data)

Upstream product

• 72342-64-4 methyl (3S)-3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methylpentanoate 
• 72212-78-3 (R)-2-(1,3-dioxoisoindolin-2-yl)-3-methylbutanoyl chloride 
• 5115-65-1 (R)-N-phthaloylvaline 
• 640-68-6 D-Val-OH 
• 866395-53-1 N-[1-(2-hydroxy-ethyl)-2-methyl-propyl]-2-hydroxymethyl-benzamide 
• 866395-48-4 (R)-1-diazo-3-phthalimido-4-methylpentan-2-one 
• 116173-94-5 (S)-3-Amino-4-methyl-pentan-1-ol 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 866395-34-8 (2S,9S,12S,19S)-2,6-cyclo-12,16-cyclo-6,10,16-triaza-19-(benzyloxycarbonylamino)-20-methyl-11-oxo-9-(2'-propyl)heneicosanoic acid methyl ester 
• 866395-31-5 (2S,9S,12S)-2,6-cyclo-12,16-cyclo-6,10,16-triaza-19-(benzyloxycarbonylamino)-11-oxo-9-(2'-propyl)nonadecanoic acid methyl ester 
• 866395-28-0 (2S,9S)-2,6-cyclo-6-aza-9-(benzyloxycarbonylamino)-10-methylundecanoic acid methyl ester 
• 866395-43-9 (S)-1-((S)-3-Benzyloxycarbonylamino-4-methyl-pentyl)-pyrrolidine-2-carboxylic acid 
• 866395-25-7 (S)-1-mesyloxy-N-(benzyloxycarbonyl)-3-amino-4-methylpentane 

Relevant articles and documents

Structure-driven design and synthesis of chiral dioxocyclam derivatives

Based on an analysis of previously reported structures and a potential geometry fit with substrates, a new family of chiral dioxocyclam derivatives have been designed. The synthesis of those ligands was accomplished starting from l-proline and α-d-amino acids (converted to β-amino acids) with a key step of macrocyclization reaction of amino esters. All ligands were converted into neutral copper(II) complexes (amide groups underwent deprotonation of upon treatment of ligands with copper(II) acetate). The complexes exhibit the desired shape of their active surfaces, as proved by X-ray analysis.