Cas 213199-75-8,Pd(C16H14N4)(C5H8ONS2)(1+)*ClO4(1-)=[Pd(C16H14N4)(C5H8ONS2)]ClO4

213199-75-8

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Basic information

Product Name: Pd(C₁₆H₁₄N₄)(C₅H₈ONS₂)⁽¹⁺⁾*ClO₄^(1-)=[Pd(C₁₆H₁₄N₄)(C₅H₈ONS₂)]ClO₄
Synonyms:
CAS NO:213199-75-8
Molecular Formula:
Molecular Weight: 630.441
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: Pd(C₁₆H₁₄N₄)(C₅H₈ONS₂)⁽¹⁺⁾*ClO₄^(1-)=[Pd(C₁₆H₁₄N₄)(C₅H₈ONS₂)]ClO₄(CAS DataBase Reference)
NIST Chemistry Reference: Pd(C₁₆H₁₄N₄)(C₅H₈ONS₂)⁽¹⁺⁾*ClO₄^(1-)=[Pd(C₁₆H₁₄N₄)(C₅H₈ONS₂)]ClO₄(213199-75-8)
EPA Substance Registry System: Pd(C₁₆H₁₄N₄)(C₅H₈ONS₂)⁽¹⁺⁾*ClO₄^(1-)=[Pd(C₁₆H₁₄N₄)(C₅H₈ONS₂)]ClO₄(213199-75-8)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 213199-75-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 213199-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,1,9 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 213199-75:
(8*2)+(7*1)+(6*3)+(5*1)+(4*9)+(3*9)+(2*7)+(1*5)=128
128 % 10 = 8
So 213199-75-8 is a valid CAS Registry Number.

213199-75-8Upstream product

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213199-75-8Relevant academic research and scientific papers

Synthesis, characterization and redox studies of (dithiocarbamato)- {N(1)-benzyl-2-(arylazo)imidazole}palladium(II) perchlorates

Das,Sinha

, p. 531 - 534 (2007/10/03)

The ternary complexes [Pd(RaaiCH2Ph) (S S)] (ClO4) (4, 5) where RaaiCH2 Ph is N (1) - benzyl - 2 - (arylazo) imidazole, [p-RC6H4N4N=NC3H2N N(1)CH2C6H5 (2); R = H (a), Me (b), Cl (c)] and (S S) = N,N-diethyldithiocarbamate (dedtc) (4) and morpholinedithiocarbamate (mdtc) (5) have been prepared and characterized on the basis of elemental analyses, IR, UV/VIS and 1H NMR data. Electrochemical studies exhibit azo group reduction.

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