1154050-04-0

Basic information

• Product Name: (p-iodobenzoyl-L-alanyl)-L-leucine
• Synonyms: (p-iodobenzoyl-L-alanyl)-L-leucine
• CAS NO: 1154050-04-0
• Molecular Weight: 432.258
• Mol File: 1154050-04-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (p-iodobenzoyl-L-alanyl)-L-leucine(CAS DataBase Reference)
• NIST Chemistry Reference: (p-iodobenzoyl-L-alanyl)-L-leucine(1154050-04-0)
• EPA Substance Registry System: (p-iodobenzoyl-L-alanyl)-L-leucine(1154050-04-0)

Safety Data

• Hazardous Substances Data: 1154050-04-0(Hazardous Substances Data)

Upstream product

• 3303-34-2 L-alanyl-L-leucine 
• 1711-02-0 4-iodobenzoic acid chloride 

Downstream Products

• 1154050-22-2 C₂₀H₂₉IN₂O₄ 
• 1154050-23-3 C₂₀H₂₉IN₂O₄ 

Relevant articles and documents

Catalytic, one-pot synthesis of β-amino acids from α-amino acids. Preparation of α,β-peptide derivatives

(Chemical Equation Presented) The one-pot conversion of readily available α-amino acid into β-amino acid derivatives was carried out in good yields. The method is a sequential process initiated by a tandem radical decarboxylation-oxidation reaction; the resulting acyliminium ion was trapped by silyl ketenes. Stoichiometric and catalytic versions of this reaction were developed and then applied to prepare modified di- and tripeptides. Interestingly, some tripeptides formed expanded β-turns in the solid state.