157077-01-5

Basic information

• Product Name: Co(C₂H₄(NCHC₆H₄O)2)(C₉H₃O₃(OCH₃)C₆H₄OCH₃)
• CAS NO: 157077-01-5
• Molecular Weight: 622.58
• Mol File: 157077-01-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Co(C₂H₄(NCHC₆H₄O)2)(C₉H₃O₃(OCH₃)C₆H₄OCH₃)(CAS DataBase Reference)
• NIST Chemistry Reference: Co(C₂H₄(NCHC₆H₄O)2)(C₉H₃O₃(OCH₃)C₆H₄OCH₃)(157077-01-5)
• EPA Substance Registry System: Co(C₂H₄(NCHC₆H₄O)2)(C₉H₃O₃(OCH₃)C₆H₄OCH₃)(157077-01-5)

Safety Data

• Hazardous Substances Data: 157077-01-5(Hazardous Substances Data)

Upstream product

• 60352-14-9 Co((CH₂NCHC₆H₄(O))2)(OH) 
• 13198-99-7 3-hydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 

Relevant articles and documents

On the Mechanism of a Model Quercetinase Reaction using a Cobalt Schiff-base Complex

Cyclic voltammetry of a substrate anion-catalyst binary complex intermediate 1> 1); H2salen = N,N'-bis(salicylidene)ethane-1,2-diamine> in a model quercetinase reaction using as catalyst has revealed that the intermediate partly undergoes ionic dissociation in dimethylformamide (dmf) to give L1 and (1+).Dioxygen is then incorporated into the flavonolate anion in a non-radical manner, which is promoted by the counter cobalt cation complex, finally to give 2(dmf)>(HL2 = a depside product) which then forms L2 and (1+).The reaction rate was affected by the nature of the cation employed: (1+) is more effective than K(1+).