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3-methyl-9,10-dioxo-9,10-dihydroanthracene-1,8-diyl diacetate is a complex organic compound with the molecular formula C18H14O6. It is derived from anthracene, a tricyclic aromatic hydrocarbon, and features a methyl group at the 3rd carbon position. The compound is characterized by two acetate groups attached to the 1st and 8th carbon positions, and a dioxo bridge between the 9th and 10th carbons, which contributes to its dihydro structure. This chemical is often used in the synthesis of various pharmaceuticals and dyes due to its unique structure and reactivity.

18713-45-6

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18713-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18713-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,1 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18713-45:
(7*1)+(6*8)+(5*7)+(4*1)+(3*3)+(2*4)+(1*5)=116
116 % 10 = 6
So 18713-45-6 is a valid CAS Registry Number.

18713-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (8-acetyloxy-6-methyl-9,10-dioxoanthracen-1-yl) acetate

1.2 Other means of identification

Product number -
Other names chrysophanol peracetate

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:18713-45-6 SDS

18713-45-6Relevant academic research and scientific papers

Synthesis of rhein and diacerein: a chemoenzymatic approach using anthrol reductase of Talaromyces islandicus

Rajput, Anshul,Mondal, Amit,Pandey, Satyendra Kumar,Husain, Syed Masood

supporting information, p. 358 - 361 (2022/01/20)

Herein, we report two methods for the synthesis of the osteoarthritis drug rhein and its prodrug diacerein using a chemoenzymatic approach. The strategy relies on the use of an NADPH-dependent anthrol reductase of Talaromyces islandicus (ARti-2), which mediates the regioselective and reductive deoxygenation of anthraquinones. The work further implies similar biosynthesis of rhein in fungi.

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