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1,8-Dihydroxy-6-methoxy-9,10-dioxo-9,10-dihydroanthracene-3-carbaldehyde is a complex organic compound with the molecular formula C17H12O7. It is a derivative of anthracene, a tricyclic aromatic hydrocarbon, and features two hydroxyl groups at the 1 and 8 positions, a methoxy group at the 6 position, and a carbaldehyde group at the 3 position. The compound also has a 9,10-dioxo group, indicating the presence of two oxygen atoms double-bonded to the carbon atoms at positions 9 and 10. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and dyes due to its unique structure and reactivity. Its chemical properties and potential applications make it an interesting subject for research in the fields of organic chemistry and materials science.

4517-57-1

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4517-57-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4517-57-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4517-57:
(6*4)+(5*5)+(4*1)+(3*7)+(2*5)+(1*7)=91
91 % 10 = 1
So 4517-57-1 is a valid CAS Registry Number.

4517-57-1SDS

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 4,5-dihydroxy-7-methoxy-9,10-dioxoanthracene-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4,5-dihydroxy-7-methoxy-9,10-dioxo-9,10-dihydro-anthracene-2-carbaldehyde

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:4517-57-1 SDS

4517-57-1Downstream Products

4517-57-1Relevant academic research and scientific papers

The synthesis, structural study and anticancer activity evaluation of emodin derivatives containing conjugative groups

Wen-Feng, Wang,Feng-Sen, Zhang,Wen-Na, Zhao,Ze-Dong, Bai,Hui-Jun, Yang,Jing-Wei, Shao,Yao-Feng, Yuan

, p. 545 - 552 (2013/07/28)

Eight new emodin derivatives that contain large conjugative system have been synthesized and their anticancer activities also have been evaluated. The result shows that large conjugative system can not enhance the anticancer activities of emodin derivativ

Chemische Studien ueber natuerliche Anthrachinone. II. Synthese von Citreoroseine, Fallacinol und Fallacinal

Hirose, Yoshio,Suehiro, Yoshihisa,Furukawa, Yumiko,Murakami, Takao

, p. 4186 - 4188 (2007/10/02)

The meltingpoint and infrared spectrum of synthesized 1,6,8-trihydroxy-3-hydroxymethylanthraquinone (II) were identical with those of citreoroseine (I) .Synthesis of 1,3-diacetoxy-3-bromomethyl-6-methoxyanthraquinone (VIII) was established.And fallacinal (V) could be prepared by oxidation of fallacinol (IV).Keywords - Penicillium citreo-roseum DIERCKX; Xanthoria fallax (HEPP.) ARN.; citreorosein; fallacinol; fallacinal; 3-formyl-1,6,8-trihydroxyanthraquinone

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