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9,10-Anthracenedione, 1,3-dihydroxy-8-methoxy-6-methyl-, also known as 1,3-Dihydroxy-8-methoxy-6-methyl-9,10-anthraquinone, is a chemical compound with the molecular formula C15H12O5. It is an anthraquinone derivative, characterized by the presence of two hydroxyl groups at the 1 and 3 positions, a methoxy group at the 8 position, and a methyl group at the 6 position. 9,10-Anthracenedione, 1,3-dihydroxy-8-methoxy-6-methyl- is known for its potential applications in the synthesis of dyes and pharmaceuticals, particularly in the production of certain anticancer drugs. It is also used as an intermediate in the preparation of other organic compounds. The compound is typically synthesized through chemical reactions involving anthraquinone and various reagents, and its properties, such as solubility and stability, can be influenced by the specific functional groups present.

3775-08-4

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3775-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3775-08-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3775-08:
(6*3)+(5*7)+(4*7)+(3*5)+(2*0)+(1*8)=104
104 % 10 = 4
So 3775-08-4 is a valid CAS Registry Number.

3775-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dihydroxy-8-methoxy-6-methylanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,3-dihydroxy-8-methoxy-6-methyl-anthracene-9,10-dione

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:3775-08-4 SDS

3775-08-4Downstream Products

3775-08-4Relevant academic research and scientific papers

Characterization of emodin metabolites in Raji cells by LC-APCI-MS/MS

Koyama, Junko,Takeuchi, Atsuko,Morita, Izumi,Nishino, Yu,Shimizu, Maki,Inoue, Munetaka,Kobayashi, Norihiro

experimental part, p. 7493 - 7499 (2011/02/23)

A rapid, simple, and sensitive liquid chromatography-atmospheric pressure chemical ionization tandem mass spectrometry (LC-APCI-MS/MS) method was developed for the identification and quantification of emodin metabolites in Raji cells, using aloe-emodin as an internal standard. Analyses were performed on an LC system employing a Cosmosil 5C18 AR-II column and a stepwise gradient elution with methanol-20 mM ammonium formate at a flow rate of 1.0 mL/min operating in the negative ion mode. As a result, the starting material emodin and its five metabolites were detected by analyzing extracts of Raji cells that had been cultivated in the presence of emodin. The identification of the metabolites and elucidation of their structures were performed by comparing their retention times and spectral patterns with those of synthetic samples. In addition to the major metabolite 8-O-methylemodin, four other metabolites were assigned as ω-hydroxyemodin, 3-O-methyl-ω-hydroxyemodin, 3-O-methylemodin (physcion), and chrysophanol.

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