Cas 62510-69-4,Cu(2+)*(CH3)2(C6H5)C3N2(O)NCHC6H4(O)(1-)*CH3COO(1-)=Cu((CH3)2(C6H5)C3N2(O)NCHC6H4(O))(CH3COO)

62510-69-4

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Basic information

Product Name: Cu⁽²⁺⁾*(CH₃)2(C₆H₅)C₃N₂(O)NCHC₆H₄(O)^(1-)*CH₃COO^(1-)=Cu((CH₃)2(C₆H₅)C₃N₂(O)NCHC₆H₄(O))(CH₃COO)
Synonyms:
CAS NO:62510-69-4
Molecular Formula:
Molecular Weight: 428.935
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Cu⁽²⁺⁾*(CH₃)2(C₆H₅)C₃N₂(O)NCHC₆H₄(O)^(1-)*CH₃COO^(1-)=Cu((CH₃)2(C₆H₅)C₃N₂(O)NCHC₆H₄(O))(CH₃COO)(CAS DataBase Reference)
NIST Chemistry Reference: Cu⁽²⁺⁾*(CH₃)2(C₆H₅)C₃N₂(O)NCHC₆H₄(O)^(1-)*CH₃COO^(1-)=Cu((CH₃)2(C₆H₅)C₃N₂(O)NCHC₆H₄(O))(CH₃COO)(62510-69-4)
EPA Substance Registry System: Cu⁽²⁺⁾*(CH₃)2(C₆H₅)C₃N₂(O)NCHC₆H₄(O)^(1-)*CH₃COO^(1-)=Cu((CH₃)2(C₆H₅)C₃N₂(O)NCHC₆H₄(O))(CH₃COO)(62510-69-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 62510-69-4(Hazardous Substances Data)

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62510-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62510-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,1 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62510-69:
(7*6)+(6*2)+(5*5)+(4*1)+(3*0)+(2*6)+(1*9)=104
104 % 10 = 4
So 62510-69-4 is a valid CAS Registry Number.

62510-69-4Upstream product

62510-69-4Downstream Products

1372673-44-3 Cu((CH₃)2(C₆H₅)C₃N₂(O)NCHC₆H₄(O))2

62510-69-4Relevant academic research and scientific papers

Oxidative dehydrogenation of N-(2-hydroxy-3,5-R1,R 2-benzyl)-4-aminoantipyrines in the complexation reaction

Medzhidov,Fatullaeva,Peng,Ismaiylov,Lee,Garaeva

, p. 126 - 133 (2012)

Reactions of N-(2-hydroxy-3,5-R1,R2-benzyl)-4- aminoantipyrines with copper acetate in ethanol gave complexes with Schiff bases (SBs) rather than the expected complexes with reduced SBs; i.e., the starting ligands undergo oxidative d

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