330624-99-2

Basic information

• Product Name: H-Ala-Tyr-Asp-Ala-Lys(Ser)-Ala-NH-CH₂-CH(OCH₃)2
• CAS NO: 330624-99-2
• Molecular Weight: 811.89
• Mol File: 330624-99-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: H-Ala-Tyr-Asp-Ala-Lys(Ser)-Ala-NH-CH₂-CH(OCH₃)2(CAS DataBase Reference)
• NIST Chemistry Reference: H-Ala-Tyr-Asp-Ala-Lys(Ser)-Ala-NH-CH₂-CH(OCH₃)2(330624-99-2)
• EPA Substance Registry System: H-Ala-Tyr-Asp-Ala-Lys(Ser)-Ala-NH-CH₂-CH(OCH₃)2(330624-99-2)

Safety Data

• Hazardous Substances Data: 330624-99-2(Hazardous Substances Data)

Upstream product

• 15761-38-3 L-N-Boc-Ala 
• 13734-38-8 N-(t-butyloxycarbonyl)-O-(t-butyl)-L-Serine 

Downstream Products

• 325814-31-1 H-Ala-Tyr-Asp-Ala-Lys(Ser)-Ala-NH-CH₂-CHO 
• 325814-33-3 H-Ala-Tyr-Asp-Ala-Lys(COCHO)-Ala-NH-CH₂-CH=NO-CH₂-CO-Asp-Ala-Arg-Ala-OH 
• 325814-32-2 H-Ala-Tyr-Asp-Ala-Lys(Ser)-Ala-NH-CH₂-CH=NO-CH₂-CO-Asp-Ala-Arg-Ala-OH 

Relevant articles and documents

Synthesis of peptide di-aldehyde precursor for stepwise chemoselective ligations via oxime bonds

To synthezise a triple-function branched peptide in a modular way, we present a new strategy based on orthogonal generation of two aldehyde functions from an acetal and a 2-amino alcohol. Successive unmaskings of aldehyde functions of the stem peptide affords stepwise chemoselective ligations of two (aminooxy)acetyl peptides via oxime bonds.