82662-00-8

Basic information

• Product Name: N-benzyloxycarbonyl-O-(N-t-butyloxycarbonyl-L-alanyl-S-acetamidomethyl-L-cysteinyl-L-valyl)-D-serine
• Synonyms: N-benzyloxycarbonyl-O-(N-t-butyloxycarbonyl-L-alanyl-S-acetamidomethyl-L-cysteinyl-L-valyl)-D-serine
• CAS NO: 82662-00-8
• Molecular Weight: 683.78
• Mol File: 82662-00-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-benzyloxycarbonyl-O-(N-t-butyloxycarbonyl-L-alanyl-S-acetamidomethyl-L-cysteinyl-L-valyl)-D-serine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyloxycarbonyl-O-(N-t-butyloxycarbonyl-L-alanyl-S-acetamidomethyl-L-cysteinyl-L-valyl)-D-serine(82662-00-8)
• EPA Substance Registry System: N-benzyloxycarbonyl-O-(N-t-butyloxycarbonyl-L-alanyl-S-acetamidomethyl-L-cysteinyl-L-valyl)-D-serine(82662-00-8)

Safety Data

• Hazardous Substances Data: 82662-00-8(Hazardous Substances Data)

Upstream product

• 82652-97-9 N-benzyloxycarbonyl-O-(N-t-butyloxycarbonyl-L-alanyl-S-acetamidomethyl-L-cysteinyl-L-valyl)-D-serine p-bromophenacyl ester 
• 713122-03-3 (Z)-D-Ser[N-Boc-L-Ala-L-Cys(Acm)-L-Val]-OTce 
• 19746-37-3 N-t-butoxycarbonyl-S-acetamidomethyl-L-cysteine 
• 82661-99-2 N-benzyloxycarbonyl-O-(N-t-butyloxycarbonyl-S-acetamidomethyl-L-cysteinyl-L-valyl)-D-serine p-bromophenacyl ester 
• 82652-96-8 N-benzyloxycarbonyl-O-(N-t-butyloxycarbonyl-L-valyl)-D-serine p-bromophenacyl ester 
• 82662-01-9 Z-D-Ser-OBpa ester 
• 713122-02-2 (Z)-D-Ser[N-Boc-Cys(Acm)-L-Val]-OTce 
• 93279-10-8 Z-D-Ser(N-Boc-L-Val)-OTce 
• 78700-43-3 Z-D-Ser(Bu^t)-OTce 
• 78700-33-1 Z-D-Ser-OTce 
• 65806-90-8 (R)-2-(((benzyloxy)carbonyl)amino)-3-(tert-butoxy)propanoic acid 
• 13734-41-3 t-Boc-L-valine 

Downstream Products

• 713122-05-5 (Z)-D-Ser{(Z)-D-Ser[Boc-L-Ala-L-Cys(Acm)-L-Val]-L-Ala-L-Cys(Acm)-L-Val}-OTce 
• 713122-07-7 C₄₉H₆₈N₈O₁₇S₂ 
• 63520-00-3 (N-benzyloxycarbonyl-D-seryl-L-alanyl-L-cysteinyl-L-valine)2(serine hydroxyl)dilactone disulfide 
• 713122-06-6 (Z)-D-Ser{(Z)-D-Ser[Boc-L-Ala-L-Cys(Acm)-L-Val]-L-Ala-L-Cys(Acm)-L-Val}-OH 
• 82667-04-7 N-benzyloxycarbonyl-O--D-serine p-bromophenacyl ester 

Relevant articles and documents

Solution-phase synthesis of nucleobase-substituted analogues of triostin A

A synthesis of novel analogues of triostin A presenting two identical or different nucleobases instead of the original quinoxaline substituents has been developed. The DNA bisintercalator triostin A (1) with its rigid backbone provides an optimal scaffold