Cas 184242-50-0,3-(4-methoxy-benzyl)-4-oxo-1-(6-vinyl-benzo[1,3]dioxol-5-ylmethyl)-1,4-dihydro-quinoline-2-carboxylic acid ethyl ester

184242-50-0

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Basic information

Product Name: 3-(4-methoxy-benzyl)-4-oxo-1-(6-vinyl-benzo[1,3]dioxol-5-ylmethyl)-1,4-dihydro-quinoline-2-carboxylic acid ethyl ester
Synonyms: 3-(4-methoxy-benzyl)-4-oxo-1-(6-vinyl-benzo[1,3]dioxol-5-ylmethyl)-1,4-dihydro-quinoline-2-carboxylic acid ethyl ester
CAS NO:184242-50-0
Molecular Formula:
Molecular Weight: 497.547
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: 3-(4-methoxy-benzyl)-4-oxo-1-(6-vinyl-benzo[1,3]dioxol-5-ylmethyl)-1,4-dihydro-quinoline-2-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-methoxy-benzyl)-4-oxo-1-(6-vinyl-benzo[1,3]dioxol-5-ylmethyl)-1,4-dihydro-quinoline-2-carboxylic acid ethyl ester(184242-50-0)
EPA Substance Registry System: 3-(4-methoxy-benzyl)-4-oxo-1-(6-vinyl-benzo[1,3]dioxol-5-ylmethyl)-1,4-dihydro-quinoline-2-carboxylic acid ethyl ester(184242-50-0)

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: 184242-50-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 184242-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,2,4 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 184242-50:
(8*1)+(7*8)+(6*4)+(5*2)+(4*4)+(3*2)+(2*5)+(1*0)=130
130 % 10 = 0
So 184242-50-0 is a valid CAS Registry Number.

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184242-50-0Relevant academic research and scientific papers

1,3-disubstituted-2-carboxyl quinolones: Highly potent and selective endothelin A receptor antagonists

Haesslein, Jean-Luc,Baholet, Isabelle,Fortin, Michel,Iltis, Alain,Khider, Jean,Periers, Anne Marie,Pierre, Christine,Vevert, Jean-Paul

, p. 1487 - 1490 (2007/10/03)

The design, synthesis, and in vitro biological activity of a series of 2-carboxy quinolone antagonists selective for the endothelin A receptor are presented. Introduction of a second acid group in position 3 of the quinolone ring increases dramatically the selectivity for ET(A). (C) 2000 Elsevier Science Ltd. All rights reserved.

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