Cas 1454647-98-3,2,9-bis-(4-amino-2,3,5,6-tetramethylphenyl)anthra[2,1,9-def;6,5,10-d′e′f ′]diisoquinolin-1,3,8,10-tetraone

1454647-98-3

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Basic information

Product Name: 2,9-bis-(4-amino-2,3,5,6-tetramethylphenyl)anthra[2,1,9-def;6,5,10-d′e′f ′]diisoquinolin-1,3,8,10-tetraone
Synonyms:
CAS NO:1454647-98-3
Molecular Formula:
Molecular Weight: 684.794
EINECS: N/A
Product Categories: N/A
Mol File: 1454647-98-3.mol
Article Data: 1

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: 2,9-bis-(4-amino-2,3,5,6-tetramethylphenyl)anthra[2,1,9-def;6,5,10-d′e′f ′]diisoquinolin-1,3,8,10-tetraone(CAS DataBase Reference)
NIST Chemistry Reference: 2,9-bis-(4-amino-2,3,5,6-tetramethylphenyl)anthra[2,1,9-def;6,5,10-d′e′f ′]diisoquinolin-1,3,8,10-tetraone(1454647-98-3)
EPA Substance Registry System: 2,9-bis-(4-amino-2,3,5,6-tetramethylphenyl)anthra[2,1,9-def;6,5,10-d′e′f ′]diisoquinolin-1,3,8,10-tetraone(1454647-98-3)

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: 1454647-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1454647-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,6,4 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1454647-98:
(9*1)+(8*4)+(7*5)+(6*4)+(5*6)+(4*4)+(3*7)+(2*9)+(1*8)=193
193 % 10 = 3
So 1454647-98-3 is a valid CAS Registry Number.

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1454647-98-3Relevant articles and documents

Chromophores arranged as "magnetic meta atoms": Building blocks for molecular metamaterials

Langhals, Heinz,Hofer, Alexander

, p. 5889 - 5897 (2013/07/26)

Benzoperylenetriscarboximides were parallel arranged by stiff spacers where exciton interactions could be controlled by their distance. The most bathochromic electronic transition of the chromophores essentially exhibits only an electric component where a

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