1263315-51-0

Basic information

• Product Name: (3R,4S) 3-(benzyloxycarbonylamino)-4-(tertbutoxycarbonylamino)-5-methylhexanoic acid
• Synonyms: (3R,4S) 3-(benzyloxycarbonylamino)-4-(tertbutoxycarbonylamino)-5-methylhexanoic acid
• CAS NO: 1263315-51-0
• Molecular Weight: 394.468
• Mol File: 1263315-51-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3R,4S) 3-(benzyloxycarbonylamino)-4-(tertbutoxycarbonylamino)-5-methylhexanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4S) 3-(benzyloxycarbonylamino)-4-(tertbutoxycarbonylamino)-5-methylhexanoic acid(1263315-51-0)
• EPA Substance Registry System: (3R,4S) 3-(benzyloxycarbonylamino)-4-(tertbutoxycarbonylamino)-5-methylhexanoic acid(1263315-51-0)

Safety Data

• Hazardous Substances Data: 1263315-51-0(Hazardous Substances Data)

Upstream product

• 944914-01-6 (4S,5S)-5-(1-methylethyl)-2-oxo-imidazolidin-4-acetic acid tert-butyl ester 
• 944913-95-5 (4R,5S)-5-(1-methylethyl)-1-phenylmethyl-2-oxo-imidazolidin-4-acetic acid tert-butyl ester 
• 944913-87-5 (S)-2-(N-benzyl-N-benzyloxycarbonylamino)-isopentanonitrile 
• 17343-55-4 (S)-N-benzyloxycarbonyl-2-amino-isopentanenitrile 
• 13139-28-1 (S)-N-benzyloxycarbonylvalinamide 
• 119153-86-5 C₁₆H₂₁NO₆ 
• 72-18-4 L-valine 
• 501-53-1 benzyl chloroformate 
• 1263315-48-5 benzyl (2S,3R)-2-isopropyl-5-oxopyrrolidin-3-ylcarbamate 
• 1263485-59-1 C₇H₁₄N₂O*ClH 
• 1263315-49-6 (2S,3R)-tert-butyl 3-(benzyloxycarbonylamino)-2-isopropyl-5-oxopyrrolidine-1-carboxylate 

Downstream Products

• 1415109-63-5 C₂₁H₃₃N₃O₅ 
• 1415109-66-8 C₂₉H₄₆N₄O₈ 
• 1415109-69-1 C₃₂H₅₂N₄O₈ 
• 1415109-71-5 C₃₅H₅₀N₄O₈ 
• 1415109-61-3 C₂₆H₄₁N₃O₇ 

Relevant articles and documents

Original β,γ-diamino acid as an inducer of a γ-turn mimic in short peptides

Original αγα tripeptides containing one β,γ-diamino acid have been synthesized and their conformation determined by extensive NMR and molecular dynamic studies. These studies revealed the presence of a C9 hydrogen bonded turn around the β,γ-diamino acid which was stabilized by bulky side chains of the preceding residue. This turn can be considered as a mimic of the well-known γ-turn. The Royal Society of Chemistry 2012.