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1,6-dihydroxy-3-(hydroxymethyl)-8-methoxyanthracene-9,10-dione is a complex organic chemical compound characterized by a six-membered anthracene ring with specific functional groups. It features two hydroxyl groups at the 1 and 6 positions, a hydroxymethyl group at position 3, and a methoxy group at position 8, all attached to the anthracene-9,10-dione core. This unique structure endows it with potential interactions with biological systems, making it a candidate for various applications in organic synthesis, medicinal chemistry, dye chemistry, material science, and the study of natural products and their analogs.

35688-09-6

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35688-09-6 Usage

Uses

Used in Organic Synthesis:
1,6-dihydroxy-3-(hydroxymethyl)-8-methoxyanthracene-9,10-dione is used as a building block in organic synthesis for the creation of novel compounds with potential applications in various fields due to its reactive functional groups and unique structural features.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1,6-dihydroxy-3-(hydroxymethyl)-8-methoxyanthracene-9,10-dione is used as a precursor or intermediate in the development of pharmaceuticals, leveraging its ability to interact with biological targets for therapeutic purposes.
Used in Dye Chemistry:
1,6-dihydroxy-3-(hydroxymethyl)-8-methoxyanthracene-9,10-dione is utilized as a dyestuff in dye chemistry, capitalizing on its structural attributes to produce colorants for various applications, including textiles, inks, and pigments.
Used in Material Science:
In material science, 1,6-dihydroxy-3-(hydroxymethyl)-8-methoxyanthracene-9,10-dione is employed in the development of new materials, potentially contributing to the creation of advanced materials with specific properties, such as optical, electronic, or mechanical characteristics.
Used in Research on Natural Products and Analogs:
1,6-dihydroxy-3-(hydroxymethyl)-8-methoxyanthracene-9,10-dione is used as a subject of study in research focused on the synthesis and properties of natural products and their analogs, providing insights into the structure-activity relationships and potential applications of similar compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 35688-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,8 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35688-09:
(7*3)+(6*5)+(5*6)+(4*8)+(3*8)+(2*0)+(1*9)=146
146 % 10 = 6
So 35688-09-6 is a valid CAS Registry Number.

35688-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-dihydroxy-3-(hydroxymethyl)-8-methoxyanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names Questinol

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:35688-09-6 SDS

35688-09-6Downstream Products

35688-09-6Relevant articles and documents

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

scheme or table, 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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