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9(10H)-Anthracenone, 10-[(3,4-dimethoxyphenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75628-90-9

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75628-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75628-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,2 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75628-90:
(7*7)+(6*5)+(5*6)+(4*2)+(3*8)+(2*9)+(1*0)=159
159 % 10 = 9
So 75628-90-9 is a valid CAS Registry Number.

75628-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-[(3,4-dimethoxyphenyl)methylidene]anthracen-9-one

1.2 Other means of identification

Product number -
Other names -

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:75628-90-9 SDS

75628-90-9Downstream Products

75628-90-9Relevant academic research and scientific papers

Characterization of a new class of androgen receptor antagonists with potential therapeutic application in advanced prostate cancer

Li, Huifang,Hassona, Mohamed D.H.,Lack, Nathan A.,Axerio-Cilies, Peter,Leblanc, Eric,Tavassoli, Peyman,Kanaan, Natalia,Frewin, Kate,Singh, Kriti,Adomat, Hans,Boehm, Konrad J.,Prinz, Helge,Guns, Emma Tomlinson,Rennie, Paul S.,Cherkasov, Artem

, p. 2425 - 2435 (2013/12/04)

The human androgen receptor plays a major role in the development and progression of prostate cancer and represents a well-established drug target. All clinically approved androgen receptor antagonists possess similar chemical structures and exhibit the s

Synthesis and antitumor activity of 10-substituted benzylidene anthrone

Hu, Weixiao,Zhou, Wei

, p. 621 - 622 (2007/10/03)

Fifteen compounds of 10-substituted benzylidene anthrone were prepared with moderate yield by reaction of anthrone and substituted benzaldehydes under the presence of pyridine and piperidine as catalyst. Their antitumor activities in vitro were evaluated.

Novel benzylidene-9(10H)-anthracenones as highly active antimicrotubule agents. Synthesis, antiproliferative activity, and inhibition of tubulin polymerization

Prinz, Helge,Ishii, Yukihito,Hirano, Takeo,Stoiber, Thomas,Camacho Gomez, Juan A.,Schmidt, Peter,Düssmann, Heiko,Burger, Angelika M.,Prehn, Jochen H. M.,Günther, Eckhard G.,Unger, Eberhard,Umezawa, Kazuo

, p. 3382 - 3394 (2007/10/03)

A novel series of 10-benzylidene-9(10H)-anthracenones and 10-(phenylmethyl)-9(10H)-anthracenones were synthesized and evaluated for antiproliferative activity in an assay based on K562 leukemia cells. The 3-hydroxy-4-methoxybenzylidene analogue 9h was fou

A facile synthesis of 10-arylmethylene anthracenones under microwave irradiation

Zhou,Tu,Feng

, p. 414 - 415 (2007/10/03)

10-Arylmethylene anthracenones were synthesised by the condensation of aromatic aldehydes with anthracenone using sodium hydroxide as catalyst under microwave irradiation in good yields.

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