87694-54-0

Basic information

• Product Name: tert-butyl ((2S,3R)-3-(benzyloxy)-1-(methoxy(methyl)amino)-1-oxobutan-2-yl)carbamate
• Synonyms: tert-butyl ((2S,3R)-3-(benzyloxy)-1-(methoxy(methyl)amino)-1-oxobutan-2-yl)carbamate
• CAS NO: 87694-54-0
• Molecular Weight: 352.431
• Mol File: 87694-54-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: tert-butyl ((2S,3R)-3-(benzyloxy)-1-(methoxy(methyl)amino)-1-oxobutan-2-yl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl ((2S,3R)-3-(benzyloxy)-1-(methoxy(methyl)amino)-1-oxobutan-2-yl)carbamate(87694-54-0)
• EPA Substance Registry System: tert-butyl ((2S,3R)-3-(benzyloxy)-1-(methoxy(methyl)amino)-1-oxobutan-2-yl)carbamate(87694-54-0)

Safety Data

• Hazardous Substances Data: 87694-54-0(Hazardous Substances Data)

Upstream product

• 15260-10-3 N-(t-Butyloxycarbonyl)-O-(phenylmethyl)-L-threonine 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 15260-10-3 N-Boc-O-benzyl-L-threonine 

Downstream Products

• 1265146-07-3 C₂₂H₃₄N₂O₆ 
• 1265146-06-2 C₂₉H₄₂N₂O₇ 
• 79069-55-9 tert-butyl [(2S,3R)-3-(benzyloxy)-1-oxobutan-2-yl]carbamate 
• 79069-55-9 N-(t-butoxycarbonyl)-O-benzyl-L-threoninal 
• 228868-10-8 ((2R,3R)-3-Benzyloxy-2-tert-butoxycarbonylamino-butylamino)-acetic acid methyl ester 

Relevant articles and documents

Synthesis of new chiral peptide nucleic acid (PNA) monomers by a simplified reductive amination method

The aim of this work was the preparation of four new peptide nucleic acid (PNA) monomer backbone by reductive amination of N(α)-Boc-protected chiral amino aldehydes, derived from Leu, Phe, Tyr(Bzl), and Thr(Bzl), with methyl glycinate. To the crude 2-subs

Pyrrole-based scaffolds for turn mimics

Two amino acid derived synthons were combined to give homopropargylic amines 2. Platinum dichloride was used to cyclize these intermediates into pyrroles 3 which collapsed to the target secondary structure mimics 1 on treatment with base. Side chains of these compounds overlay with an idealized type 1 β-turn and with an inverse γ-turn.(Figure Presented)