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2,5-Cyclohexadiene-1,4-dione, 2-methyl-6-(phenylamino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57675-10-2

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57675-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57675-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,7 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57675-10:
(7*5)+(6*7)+(5*6)+(4*7)+(3*5)+(2*1)+(1*0)=152
152 % 10 = 2
So 57675-10-2 is a valid CAS Registry Number.

57675-10-2SDS

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 2-anilino-6-methylcyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-anilino-6-methylbenzoquinone

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:57675-10-2 SDS

57675-10-2Downstream Products

57675-10-2Relevant academic research and scientific papers

Synthesis of carbazoloquinone derivatives and their antileukemic activity via modulating cellular reactive oxygen species

Suematsu, Natsumi,Ninomiya, Masayuki,Sugiyama, Hodaka,Udagawa, Taro,Tanaka,Koketsu, Mamoru

, p. 2243 - 2247 (2019/07/03)

Carbazoloquinone alkaloids are of great interest as privileged structures for anticancer drug molecules. The purpose of this study was to investigate the structure-activity relationships of carbazoloquinone derivatives as anticancer agents. A series of ca

An in-water, on-water domino process for synthesis

Norcott, Philip,Spielman, Calan,McErlean, Christopher S. P.

supporting information; experimental part, p. 605 - 609 (2012/04/23)

An in-water, on-water domino process has been engineered as a green strategy for chemical synthesis. The process is driven by the different aqueous solubility of organic reactants and products, which are shuttled between the two phases of an emulsion. During this process, water serves as a reaction medium, a product partitioner and a reaction catalyst. The Royal Society of Chemistry 2012.

Structure-activity delineation of quinones related to the biologically active Calothrixin B

Bernardo, Paul H.,Chai, Christina L.L.,Guen, Maurice Le,Smith, Geoffrey D.,Waring, Paul

, p. 82 - 85 (2007/10/03)

Quinones such as Calothrixins A and B display a range of biological properties. As part of our ongoing studies to elucidate the mechanism of action of the Calothrixins, several related quinones were synthesized and tested for biological activity. The resu

Indoloquinones, part 8.1 palladium(II)-catalyzed total synthesis of murrayaquinone A, koeniginequinone A, and koeniginequinone B

Knoelker, Hans-Joachim,Reddy, Kethiri R.

, p. 1049 - 1052 (2007/10/03)

Regioselective addition of the appropriate arylamines to 2-methyl-1,4-benzoquinone followed by a palladium(II)-catalyzed oxidative cyclization opens up an efficient route to the naturally occurring 3-methylcarbazole-1,4-quinone alkaloids murrayaquinone A, koeniginequinone A, and koeniginequinone B.

Catalytic oxidative aromatic cyclizations with palladium

Akermark, Bjoern,Oslob, Johan D.,Heuschert, Ulrich

, p. 1325 - 1326 (2007/10/02)

Using tert-butyl hydroperoxide as oxidant, facile palladium-catalyzed cyclizations of arylaminoquinones have been performed.

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