682774-41-0

Basic information

• Product Name: 5,7-Dioxa-2-aza-10-silaundecanoic acid, 10,10-dimethyl-3-(phenylmethyl)-, 1,1-dimethylethyl ester, (3S)-
• CAS NO: 682774-41-0
• Molecular Formula: C20H35NO4Si
• Molecular Weight: 381.588
• Mol File: 682774-41-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5,7-Dioxa-2-aza-10-silaundecanoic acid, 10,10-dimethyl-3-(phenylmethyl)-, 1,1-dimethylethyl ester, (3S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 5,7-Dioxa-2-aza-10-silaundecanoic acid, 10,10-dimethyl-3-(phenylmethyl)-, 1,1-dimethylethyl ester, (3S)-(682774-41-0)
• EPA Substance Registry System: 5,7-Dioxa-2-aza-10-silaundecanoic acid, 10,10-dimethyl-3-(phenylmethyl)-, 1,1-dimethylethyl ester, (3S)-(682774-41-0)

Safety Data

• Hazardous Substances Data: 682774-41-0(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 651036-89-4 [2-borono-1-(S)-(2-trimethylsilanyl-ethoxymethoxymethyl)-ethyl]-carbamic acid tert-butyl ester 
• 591-50-4 iodobenzene 
• 651036-12-3 [2-(R)-chloro-1-(2-trimethylsilanyl-ethoxymethoxymethyl)-ethyl]-carbamic acid tert-butyl ester 
• 651035-90-4 (2-(R)-chloro-1-hydroxymethyl-ethyl)-carbamic acid tert-butyl ester 
• 651035-84-6 2-(R)-tert-butoxycarbonylamino-3-chloro-propionic acid methyl ester 
• 2766-43-0 N-tert-butyloxycarbonyl-L-serine methyl ester 

Downstream Products

• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 51987-73-6 (S)-2-tert-butoxycarbonylamino-3-phenyl-propionic acid methyl ester 
• 17585-69-2 L-phenylalanine hydrochloride 
• 65615-89-6 methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(4-nitrophenyl)propanoate 
• 66605-57-0 (S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol 

Relevant articles and documents

Highly functionalised organolithium and organoboron reagents for the preparation of enantiomerically pure α-amino acids

Homochiral, highly functionalised organolithium reagents derived from l-serine have been generated and reacted with electrophiles. The novel enantiomerically pure adducts thus obtained were then converted, through β-amino alcohols, into novel non-proteinogenic α-amino acids. The methodology also made available a novel boronic acid which was then employed as a Suzuki cross-coupling partner, elaborating a new pathway to phenylalanine analogues.