18668-10-5

Basic information

• Product Name: N-Benzyloxycarbonyl-N-methyl-D-Val-D-α-hydroxy-isovaleriansaeure-tert.-butylester
• CAS NO: 18668-10-5
• Molecular Weight: 421.534
• Mol File: 18668-10-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-Benzyloxycarbonyl-N-methyl-D-Val-D-α-hydroxy-isovaleriansaeure-tert.-butylester(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzyloxycarbonyl-N-methyl-D-Val-D-α-hydroxy-isovaleriansaeure-tert.-butylester(18668-10-5)
• EPA Substance Registry System: N-Benzyloxycarbonyl-N-methyl-D-Val-D-α-hydroxy-isovaleriansaeure-tert.-butylester(18668-10-5)

Safety Data

• Hazardous Substances Data: 18668-10-5(Hazardous Substances Data)

Upstream product

• 53978-73-7 Z-D-MeVal 
• 4216-96-0 (-)-tert-butyl 2-hydroxy-3-methylbutanoate 
• 868740-08-3 D-α-Acetoxy-isovaleriansaeure-tert-butylester 
• 501-53-1 benzyl chloroformate 
• 2480-23-1 N-methyl-L-valine 
• 640-68-6 D-Val-OH 
• 44976-78-5 (R)-2-acetoxy-3-methylbutanoic acid 
• 26782-75-2 2S-2-bromo-3-methylbutanoic acid 
• 72-18-4 L-valine 
• 42417-65-2 Z-MeVal-OH 
• 3519-30-0 L-α-hydroxyisovaleric acid t-butyl ester 

Downstream Products

• 18668-12-7 2-(N-benzyloxycarbonyl-N-methylamino)-3-methylbutyric acid 1-carboxy-2-methylpropyl ester 
• 18668-12-7 N-Benzyloxycarbonyl-N-methyl-L-Val-D-α-hydroxy-isovaleriansaeure 
• 18668-12-7 N-Benzyloxycarbonyl-N-methyl-D-Val-D-α-hydroxy-isovaleriansaeure 
• 18671-23-3 N-Benzyloxycarbonyl-N-methyl-L-Val-L-α-hydroxy-isovaleryl-N-methyl-L-Val-L-α-hydroxy-isovaleriansaeure-tert.-butylester 
• 18671-23-3 N-Benzyloxycarbonyl-N-methyl-L-Val-D-α-hydroxy-isovaleryl-N-methyl-L-Val-D-α-hydroxy-isovaleriansaeure-tert.-butylester 
• 18671-23-3 N-Benzyloxycarbonyl-N-methyl-D-Val-D-α-hydroxy-isovaleryl-N-methyl-D-Val-D-α-hydroxy-isovaleriansaeure-tert.-butylester 
• 18671-27-7 N-Benzyloxycarbonyl-N-methyl-L-Val-D-α-hydroxy-isovaleryl-N-methyl-L-Val-D-α-hydroxy-isovaleryl-N-methyl-L-Val-D-α-hydroxy-isovaleriansaeure-tert.-butylester 

Relevant articles and documents

STEREOSELEKTIVE SYNTHESE VON D-α-HYDROXYCARBONSAEUREN BZW. D-α-HYDROXYCARBONSAEUREN ENTHALTENDEN DEPSIPEPTIDEN AUS L-AMINOSAEUREN

Depsipeptides containing D-α-hydroxy carboxylic acids are efficiently synthesized by the reactions of L-α-halo-carboxylic acid esters (obtained from L-amino acids) with caesium salts of N-protected amino acids.