Cas 954374-16-4,5-amino-N-[1-(4-tert-butylphenoxy)-9,10-anthraquinon-2-yl]-N'-(2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecen-15-yl)isophthalamide

954374-16-4

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Basic information

Product Name: 5-amino-N-[1-(4-tert-butylphenoxy)-9,10-anthraquinon-2-yl]-N'-(2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecen-15-yl)isophthalamide
Synonyms: 5-amino-N-[1-(4-tert-butylphenoxy)-9,10-anthraquinon-2-yl]-N'-(2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecen-15-yl)isophthalamide
CAS NO:954374-16-4
Molecular Formula:
Molecular Weight: 799.877
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: 5-amino-N-[1-(4-tert-butylphenoxy)-9,10-anthraquinon-2-yl]-N'-(2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecen-15-yl)isophthalamide(CAS DataBase Reference)
NIST Chemistry Reference: 5-amino-N-[1-(4-tert-butylphenoxy)-9,10-anthraquinon-2-yl]-N'-(2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecen-15-yl)isophthalamide(954374-16-4)
EPA Substance Registry System: 5-amino-N-[1-(4-tert-butylphenoxy)-9,10-anthraquinon-2-yl]-N'-(2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecen-15-yl)isophthalamide(954374-16-4)

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: 954374-16-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 954374-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,4,3,7 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 954374-16:
(8*9)+(7*5)+(6*4)+(5*3)+(4*7)+(3*4)+(2*1)+(1*6)=194
194 % 10 = 4
So 954374-16-4 is a valid CAS Registry Number.

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954374-16-4Relevant academic research and scientific papers

Synthesis of photoactive polyfunctional molecules based on 1-aryloxyanthraquinone aminoderivatives

Klimenko,Kusov,Vlasov

, p. 1690 - 1695 (2007/10/03)

By alternating stages of condensation of 1-(4-tert-butylphenoxy)-2-amino-9, 10-anthraquinone with 5-nitroisophthaloyl dichloride, cyanuric chloride, and 4-aminobenzocrown ethers with stages of catalytic reduction of nitro group photoactive polyfunctional

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