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Pyrido[2,3-g]quinoline-5,10-dione, 4-chloro-9-(2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

191849-09-9

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191849-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191849-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,8,4 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 191849-09:
(8*1)+(7*9)+(6*1)+(5*8)+(4*4)+(3*9)+(2*0)+(1*9)=169
169 % 10 = 9
So 191849-09-9 is a valid CAS Registry Number.

191849-09-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-9-(2-nitrophenyl)pyrido[2,3-g]quinoline-5,10-dione

1.2 Other means of identification

Product number -
Other names 4-chloro-8-(o-nitrophenyl)-1,5-diazaanthraquinone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:191849-09-9 SDS

191849-09-9Relevant academic research and scientific papers

Synthesis and biological evaluation of new 1,5-diazaanthraquinones with cytotoxic activity

Manzanaro, Sonia,Vicent, María Jesús,Martín, María Jesús,Salvador-Tormo, Nélida,Pérez, José María,Del Mar Blanco, María,Avenda?o, Carmen,Menéndez, José Carlos,De La Fuente, Jesús ángel

, p. 6505 - 6515 (2007/10/03)

A series of 1,5-diazaanthraquinone derivatives was synthesized and their in vitro cytotoxic activities were evaluated against several human cancer cell lines. The 1,5-diazaanthraquinone chromophore has been synthesized either on the basis of hetero Diels-

A C-ring regioisomer of the marine alkaloid meridine exhibits selective in vitro cytotoxicity for solid tumours

ángel de la Fuente, Jesús,Jesús Martín, Ma,Del Mar Blanco, Ma,Pascual-Alfonso, Eva,Avendao, Carmen,Carlos Menéndez

, p. 1807 - 1814 (2007/10/03)

9-Hydroxybenzo[b]pyrido[4,3,2-de](1,10)-phenantrolin-8-one (1) a regioisomer of the marine alkaloid meridine, was synthesized from 5,8-dimethoxy-6-nitro-4(1H)-quinolinone in eight steps and 23% overall yield. A shorter route was also investigated, based o

Synthesis of meridine, cystodamine, and related compounds including iminoquinolinequinone structure

Kitahara, Yoshiyasu,Tamura, Fumiyasu,Nishimura, Miki,Kubo, Akinori

, p. 8421 - 8432 (2007/10/03)

Two aromatic alkaloids, meridine (1) and cystodamine (3), and related compounds (2, 4, 5) were synthesized by hetero Diels-Alder reaction between 4-methoxy- (or 4-chloro-)5,8-quinolinedione and 2-nitrocinnamaldehyde dimethylhydrazone.

Synthesis of cystodamine, a pentacyclic aza-aromatic alkaloid

Kitahara, Yoshiyasu,Tamura, Fumiyasu,Kubo, Akinori

, p. 4441 - 4442 (2007/10/03)

A pentacyclic aza-aromatic alkaloid, cystodamine (6), and its isomer (11) were synthesized from 7-(or 6-)bromo-4-chloro-5,8-quinolinedione (1,8) and o-nitrocinnamaldehyde dimethylhydrazone (2) using hetero Diels-Alder reaction.

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