587829-04-7

Basic information

• Product Name: [Ni(NC₅H₄C(O)NC₆H₄C(C₆H₅)NCH(CH₃)C(O)O)]
• CAS NO: 587829-04-7
• Molecular Weight: 430.085
• Mol File: 587829-04-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [Ni(NC₅H₄C(O)NC₆H₄C(C₆H₅)NCH(CH₃)C(O)O)](CAS DataBase Reference)
• NIST Chemistry Reference: [Ni(NC₅H₄C(O)NC₆H₄C(C₆H₅)NCH(CH₃)C(O)O)](587829-04-7)
• EPA Substance Registry System: [Ni(NC₅H₄C(O)NC₆H₄C(C₆H₅)NCH(CH₃)C(O)O)](587829-04-7)

Safety Data

• Hazardous Substances Data: 587829-04-7(Hazardous Substances Data)

Upstream product

• 124522-52-7 pyridine-2-carboxylic acid(2-benzoyl-phenyl)-amide 
• 302-72-7 rac-Ala-OH 
• 6018-89-9 nickel(II) acetate tetrahydrate 

Downstream Products

• 134644-29-4 [Ni(NC₅H₄C(O)NC₆H₄C(C₆H₅)NC(CH₃)(CH₂C₆H₅)C(O)O)] 

Relevant articles and documents

Preparation of labeled aromatic amino acids: Via late-stage18F-fluorination of chiral nickel and copper complexes

A general protocol for the preparation of 18F-labeled AAAs and α-methyl-AAAs applying alcohol-enhanced Cu-mediated radiofluorination of Bpin-substituted chiral complexes using Ni/Cu-BPX templates as double protecting groups is reported. The chiral auxiliaries are easily accessible from commercially available starting materials in a few synthetic steps. The versatility of the method was demonstrated by the high-yielding preparation of a series of [18F]F-AAAs and the successful implementation of the protocol into automated radiosynthesis modules. This journal is