916049-73-5

Basic information

• Product Name: 2-((3-benzyloxy-2-tert-butoxycarbonylaminopropionyl){[(2,4-dimethoxyphenyl)dimethylphenylsilanyl]methyl}amino)-3-phenylpropionic acid methyl ester
• Synonyms: 2-((3-benzyloxy-2-tert-butoxycarbonylaminopropionyl){[(2,4-dimethoxyphenyl)dimethylphenylsilanyl]methyl}amino)-3-phenylpropionic acid methyl ester
• CAS NO: 916049-73-5
• Molecular Weight: 664.871
• Mol File: 916049-73-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-((3-benzyloxy-2-tert-butoxycarbonylaminopropionyl){[(2,4-dimethoxyphenyl)dimethylphenylsilanyl]methyl}amino)-3-phenylpropionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-((3-benzyloxy-2-tert-butoxycarbonylaminopropionyl){[(2,4-dimethoxyphenyl)dimethylphenylsilanyl]methyl}amino)-3-phenylpropionic acid methyl ester(916049-73-5)
• EPA Substance Registry System: 2-((3-benzyloxy-2-tert-butoxycarbonylaminopropionyl){[(2,4-dimethoxyphenyl)dimethylphenylsilanyl]methyl}amino)-3-phenylpropionic acid methyl ester(916049-73-5)

Safety Data

• Hazardous Substances Data: 916049-73-5(Hazardous Substances Data)

Upstream product

• 66866-45-3 C₂₀H₂₉NO₇ 
• 609347-83-3 2-({[(2,4-dimethoxyphenyl)dimethylphenylsilanyl]methyl}amino)-3-phenylpropionic acid methyl ester 
• 609347-79-7 (chloromethyl)dimethyl(2,4-dimethoxyphenyl)silane 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 23680-31-1 BOC-O-benzyl-L-serine 
• 17715-69-4 1-Bromo-2,4-dimethoxybenzene 

Relevant articles and documents

Building functionalized peptidomimetics: Use of electroauxiliaries for introducing N-acyliminium ions into peptides

A series of silyl-substituted amino acids have been synthesized, inserted into peptides, and then employed as precursors for oxidatively generating reactive N-acyliminium ions. Both electrochemical and chemical oxidation procedures have been employed. N-Acyliminium ion generation in a solid-phase substrate as well as application to a small library of functionalized dipeptides has been demonstrated. Limitations in terms of how electron-rich the silyl groups can be as well as the compatibility of multiple silyl groups within a longer peptide are defined.