71096-62-3

Basic information

• Product Name: β-(6-benzylaminopurin-9-yl)alanine
• CAS NO: 71096-62-3
• Molecular Weight: 312.331
• Mol File: 71096-62-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: β-(6-benzylaminopurin-9-yl)alanine(CAS DataBase Reference)
• NIST Chemistry Reference: β-(6-benzylaminopurin-9-yl)alanine(71096-62-3)
• EPA Substance Registry System: β-(6-benzylaminopurin-9-yl)alanine(71096-62-3)

Safety Data

• Hazardous Substances Data: 71096-62-3(Hazardous Substances Data)

Upstream product

• 84856-32-6 (S)-2-Amino-3-(5-amino-6-chloro-pyrimidin-4-ylamino)-propionic acid 
• 84894-26-8 (S)-2-Amino-3-(6-chloro-purin-9-yl)-propionic acid; hydrochloride 
• 100-46-9 benzylamine 
• 5429-56-1 N-Acetamidoacrylic acid 
• 1214-39-7 6-benzyladenine 
• 5147-00-2 O-acetyl-L-serine 
• 56-45-1 L-serin 

Relevant articles and documents

Biomimetic Synyhesis of Heterocyclic β-Substituted Alanines by Pyridoxal 5'-Phosphate-Catalyzed Chemical Reactions

Several heterocyclic β-substituted alanines were biomimetically synthesized by incubating 0.1M acetate buffer solution containing the appropriate heterocyclic compound and O-acetylserine or serine in the presence of pyridoxal 5'-phosphate (PLP) and metal ions.This PLP-catalyzed chemical reaction depends upon pH, metal ions and temperature.The addition of Ga3+, Fe3+ or Al3+ enhanced the rate of synthesis.The optimum of the various reaction conditions of this biomimetic method is described.Keywords - biomymetic synthesis; amino acid synthesis; heterocyclic β-substituted alanine; non-protein amino acid; O-acetylserine; N-heterocyclic compound; pyridoxal 5'-phosphate; metal ion

BIOSYNTHESIS OF β-(6-BENZYLAMINOPUTIN-9-YL)ALANINE, A METABOLITE OF VYTOKININ 6-BENZYLAMINOPURINE IN HIGHER PLANTS

β-(6-benzylaminopurin-9-yl)alanine (3), a metabolite of the cytokinin 6-benzylaminopurine (2), was confirmed to be derived from O-acetyl-L-serine (1) and (2) by an enzyme in higher plants.Some properties of the enzyme are described.