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5,8-Quinolinedione, 4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

199281-61-3

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199281-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199281-61-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,2,8 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 199281-61:
(8*1)+(7*9)+(6*9)+(5*2)+(4*8)+(3*1)+(2*6)+(1*1)=183
183 % 10 = 3
So 199281-61-3 is a valid CAS Registry Number.

199281-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylquinoline-5,8-dione

1.2 Other means of identification

Product number -
Other names 5,8-Quinolinedione,4-phenyl

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:199281-61-3 SDS

199281-61-3Relevant 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-

Synthesis of 5,8- and 5,6-quinolinediones using oxidative demethylation with cerium(IV) ammonium nitrate

Kitahara, Yoshiyasu,Nagatsu, Masanori,Shibano, Yoshikazu,Kubo, Akinori

, p. 1697 - 1701 (2007/10/03)

4-Phenyl-5,8-quinolinediones (7, 8, 12, 13), 4-phenyl-5,6- quinolinediones (9, 14), and 2-dialkylamino-4-phenyl-5,8-quinolinediones (17, 18), were synthesized by oxidative demethylation of the corresponding 5,8- dimethoxy- or 5,6,8-trimethoxy-4-phenylquin

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