Cas 376647-06-2,[2(1),2(8),7(1),7(8)-tetraphenyldianthraco[b,g]-12,13,17,18-tetraphenyl-5,10,15,20-tetraazaporphyrinato(2-)]cobalt(II)

376647-06-2

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Basic information

Product Name: [2⁽¹⁾,2⁽⁸⁾,7⁽¹⁾,7⁽⁸⁾-tetraphenyldianthraco[b,g]-12,13,17,18-tetraphenyl-5,10,15,20-tetraazaporphyrinato^(2-)]cobalt(II)
Synonyms:
CAS NO:376647-06-2
Molecular Formula:
Molecular Weight: 1280.43
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: [2⁽¹⁾,2⁽⁸⁾,7⁽¹⁾,7⁽⁸⁾-tetraphenyldianthraco[b,g]-12,13,17,18-tetraphenyl-5,10,15,20-tetraazaporphyrinato^(2-)]cobalt(II)(CAS DataBase Reference)
NIST Chemistry Reference: [2⁽¹⁾,2⁽⁸⁾,7⁽¹⁾,7⁽⁸⁾-tetraphenyldianthraco[b,g]-12,13,17,18-tetraphenyl-5,10,15,20-tetraazaporphyrinato^(2-)]cobalt(II)(376647-06-2)
EPA Substance Registry System: [2⁽¹⁾,2⁽⁸⁾,7⁽¹⁾,7⁽⁸⁾-tetraphenyldianthraco[b,g]-12,13,17,18-tetraphenyl-5,10,15,20-tetraazaporphyrinato^(2-)]cobalt(II)(376647-06-2)

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: 376647-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 376647-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,6,6,4 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 376647-06:
(8*3)+(7*7)+(6*6)+(5*6)+(4*4)+(3*7)+(2*0)+(1*6)=182
182 % 10 = 2
So 376647-06-2 is a valid CAS Registry Number.

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376647-06-2Relevant academic research and scientific papers

Mono-aromatic ring-fused versus adjacently di-aromatic ring-fused tetraazaporphyrins: Regioselective synthesis and their spectroscopic and electrochemical properties

Kobayashi, Nagao,Fukuda, Takamitsu

, p. 8021 - 8034 (2007/10/03)

A method which preferentially produces adjacently di-aromatic ring-substituted tetraazaporphyrins (TAPs) has been developed, and their electrochemical and spectroscopic properties have been studied and compared with those of the corresponding series of mo

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