Cas 866236-26-2,N,N'-bis(2,6-diisopropylphenyl)-1,7-di(2-bromophenyl)-3,4:9,10-perylene tetracarboxdiimide

866236-26-2

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Basic information

Product Name: N,N'-bis(2,6-diisopropylphenyl)-1,7-di(2-bromophenyl)-3,4:9,10-perylene tetracarboxdiimide
Synonyms: N,N'-bis(2,6-diisopropylphenyl)-1,7-di(2-bromophenyl)-3,4:9,10-perylene tetracarboxdiimide
CAS NO:866236-26-2
Molecular Formula:
Molecular Weight: 1020.86
EINECS: N/A
Product Categories: N/A
Mol File: 866236-26-2.mol
Article Data: 2

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: N,N'-bis(2,6-diisopropylphenyl)-1,7-di(2-bromophenyl)-3,4:9,10-perylene tetracarboxdiimide(CAS DataBase Reference)
NIST Chemistry Reference: N,N'-bis(2,6-diisopropylphenyl)-1,7-di(2-bromophenyl)-3,4:9,10-perylene tetracarboxdiimide(866236-26-2)
EPA Substance Registry System: N,N'-bis(2,6-diisopropylphenyl)-1,7-di(2-bromophenyl)-3,4:9,10-perylene tetracarboxdiimide(866236-26-2)

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: 866236-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 866236-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,2,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 866236-26:
(8*8)+(7*6)+(6*6)+(5*2)+(4*3)+(3*6)+(2*2)+(1*6)=192
192 % 10 = 2
So 866236-26-2 is a valid CAS Registry Number.

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866236-26-2Relevant articles and documents

Facile synthetic approach to novel core-extended perylene carboximide dyes

Mueller, Sibylle,Muellen, Klaus

, p. 4045 - 4046 (2005)

The straightforward synthesis of two new classes of core-extended perylene chromophores, dibenzocoronene tetracarboxdiimide and indenoperylene dicarboxmonoimide, proves that directional enlargement of the aromatic π-system leads to tailored bathochromic a

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