Cas 455251-65-7,9-chloro-4-[N-(3-(N-([1,10]phenanthrolin-5-yl)-N-(p-toluenesulfonyl)amino)propyl)carboxamido]acridine

455251-65-7

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Basic information

Product Name: 9-chloro-4-[N-(3-(N-([1,10]phenanthrolin-5-yl)-N-(p-toluenesulfonyl)amino)propyl)carboxamido]acridine
Synonyms: 9-chloro-4-[N-(3-(N-([1,10]phenanthrolin-5-yl)-N-(p-toluenesulfonyl)amino)propyl)carboxamido]acridine
CAS NO:455251-65-7
Molecular Formula:
Molecular Weight: 646.169
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: 9-chloro-4-[N-(3-(N-([1,10]phenanthrolin-5-yl)-N-(p-toluenesulfonyl)amino)propyl)carboxamido]acridine(CAS DataBase Reference)
NIST Chemistry Reference: 9-chloro-4-[N-(3-(N-([1,10]phenanthrolin-5-yl)-N-(p-toluenesulfonyl)amino)propyl)carboxamido]acridine(455251-65-7)
EPA Substance Registry System: 9-chloro-4-[N-(3-(N-([1,10]phenanthrolin-5-yl)-N-(p-toluenesulfonyl)amino)propyl)carboxamido]acridine(455251-65-7)

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: 455251-65-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 455251-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,5,2,5 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 455251-65:
(8*4)+(7*5)+(6*5)+(5*2)+(4*5)+(3*1)+(2*6)+(1*5)=147
147 % 10 = 7
So 455251-65-7 is a valid CAS Registry Number.

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455251-65-7Relevant academic research and scientific papers

Design of site specific DNA damaging agents for generation of multiply damaged sites

Martelli, Alain,Constant, Jean-Francois,Demeunynck, Martine,Lhomme, Jean,Dumy, Pascal

, p. 4291 - 4298 (2007/10/03)

We describe the synthesis and DNA damaging activities of hybrid molecules in which a purine (adenine) is linked to an intercalating chromophore (acridine) by a polyamino linker. A DNA damaging agent, phenanthroline or para-nitrobenzamide, is tethered to the acridine moiety at various positions. Our goal is to induce upon activation other lesions in close proximity to the abasic site and therefore create cytotoxic multiply damaged sites.

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