86645-64-9

Basic information

• Product Name: iBuOCO-Lys(Z)-OMe
• CAS NO: 86645-64-9
• Molecular Weight: 394.468
• Mol File: 86645-64-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: iBuOCO-Lys(Z)-OMe(CAS DataBase Reference)
• NIST Chemistry Reference: iBuOCO-Lys(Z)-OMe(86645-64-9)
• EPA Substance Registry System: iBuOCO-Lys(Z)-OMe(86645-64-9)

Safety Data

• Hazardous Substances Data: 86645-64-9(Hazardous Substances Data)

Upstream product

• 55355-50-5 N^ω-benzyloxycarbonyl-(RS)-lysine methyl ester hydrochloride 
• 66866-44-2 C₁₆H₂₉NO₆ 
• 66866-47-5 C₁₆H₂₉NO₆ 
• 27894-50-4 methyl (2S)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoate hydrochloride 
• 543-27-1 isobutyl chloroformate 
• 41446-04-2 Z-Ile-O-COOiBu 
• 66866-47-5 Boc-Ile-O-COOiBu 
• 45170-31-8 Boc-N-Me-Val-OH 
• 53363-89-6 N-t-butoxycarbonyl-N-methyl-L-leucine 
• 33099-08-0 N-benzyloxycarbonyl-N-methyl-L-leucine 
• 42417-65-2 Z-MeVal-OH 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 2018-66-8 Z-Leu-OH 

Relevant articles and documents

MIXED ANHYDRIDES IN PEPTIDE SYNTHESIS. A STUDY URETHANE FORMATION WITH A CONTRIBUTION ON MINIMIZATION OF RACEMIZATION

A study of the factors contributing to urethane formation during the coupling of N-alkoxycarbonylamino acids with an amino acid ester by the mixed carboxylic-carbonic acid anhydride method has been carried out, using nuclear magnetic resonance spectroscop

Mixed Anhydrides in Peptide Synthesis. Reduction of Urethane Formation and Racemization Using N-Methylpiperidine as the Tertiary Amine Base

The side reactions of urethane formation and racemization accompanying couplings by the mixed anhydride method are reduced when N-methylpiperidine is used as base, the best results being achieved in dichloromethane.