Cas 1187065-46-8,5-(4-(3-(thiophen-2-yl)benzamido)phenyl)-N-(3-(dimethylamino)propyl)thiophene-2-carboxamide

1187065-46-8

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Basic information

Product Name: 5-(4-(3-(thiophen-2-yl)benzamido)phenyl)-N-(3-(dimethylamino)propyl)thiophene-2-carboxamide
Synonyms: 5-(4-(3-(thiophen-2-yl)benzamido)phenyl)-N-(3-(dimethylamino)propyl)thiophene-2-carboxamide
CAS NO:1187065-46-8
Molecular Formula:
Molecular Weight: 489.662
EINECS: N/A
Product Categories: N/A
Mol File: 1187065-46-8.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: 5-(4-(3-(thiophen-2-yl)benzamido)phenyl)-N-(3-(dimethylamino)propyl)thiophene-2-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 5-(4-(3-(thiophen-2-yl)benzamido)phenyl)-N-(3-(dimethylamino)propyl)thiophene-2-carboxamide(1187065-46-8)
EPA Substance Registry System: 5-(4-(3-(thiophen-2-yl)benzamido)phenyl)-N-(3-(dimethylamino)propyl)thiophene-2-carboxamide(1187065-46-8)

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: 1187065-46-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1187065-46-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,0,6 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1187065-46:
(9*1)+(8*1)+(7*8)+(6*7)+(5*0)+(4*6)+(3*5)+(2*4)+(1*6)=168
168 % 10 = 8
So 1187065-46-8 is a valid CAS Registry Number.

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1187065-46-8Relevant articles and documents

Biaryl polyamides as a new class of DNA quadruplex-binding ligands

Rahman, Khondaker M.,Reszka, Anthony P.,Gunaratnam, Mekala,Haider, Shozeb M.,Howard, Philip W.,Fox, Keith R.,Neidle, Stephen,Thurston, David E.

, p. 4097 - 4099 (2009)

We report a novel class of biaryl polyamides highly selective for G-quadruplex DNA, and with significant cytotoxicity in several cancer cell lines; they form planar U-shaped structures that match the surface area dimensions of a terminal G-quartet in quadruplex structures rather than the grooves of duplex DNA.

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