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4-(5,6,7,8-tetramethoxy-4-oxo-4H-chromen-2-yl)phenyl acetate is a complex organic compound with the molecular formula C20H18O8. It is a derivative of the flavone class of flavonoids, characterized by a 4H-chromen-4-one core structure with four methoxy groups at positions 5, 6, 7, and 8. The molecule features a phenyl ring at position 4, which is further esterified with an acetate group. 4-(5,6,7,8-tetramethoxy-4-oxo-4H-chromen-2-yl)phenyl acetate is known for its potential biological activities, such as antioxidant and anti-inflammatory properties, and is found in various plants. It is also used in the synthesis of pharmaceuticals and as a research tool in studying the structure-activity relationships of flavonoids. Due to its chemical complexity, it is typically synthesized through multi-step organic reactions and is of interest in the field of natural product chemistry and drug development.

6959-55-3

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6959-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6959-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6959-55:
(6*6)+(5*9)+(4*5)+(3*9)+(2*5)+(1*5)=143
143 % 10 = 3
So 6959-55-3 is a valid CAS Registry Number.

6959-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(acetyloxy)phenyl]-5,6,7,8-tetramethoxy-4H-1-benzopyran-4-one

1.2 Other means of identification

Product number -
Other names [4-(5,6,7,8-tetramethoxy-4-oxochromen-2-yl)phenyl] acetate

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6959-55-3 SDS

6959-55-3Downstream Products

6959-55-3Relevant academic research and scientific papers

Biotransformation of polymethoxylated flavonoids: Access to their 4′-O-demethylated metabolites

Buisson, Didier,Quintin, Jerome,Lewin, Guy

, p. 1035 - 1038 (2008/02/13)

Regioselective O-demethylation of the flavones tangeretin (1) and 3-hydroxytangeretin (6) into their 4′-O-demethylated metabolites was performed by using an Aspergillus niger strain. This method serves as a straightforward alternative to multistep synthes

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