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3-(3,4-dimethoxyphenyl)-2-oxo-2H-chromen-7-yl acetate is a complex organic compound with the molecular formula C18H14O7. It is a derivative of the flavonoid family, characterized by the presence of a chromene ring system with a 3,4-dimethoxyphenyl group at the 3-position and an acetate group at the 7-position. 3-(3,4-dimethoxyphenyl)-2-oxo-2H-chromen-7-yl acetate exhibits various biological activities, such as antioxidant, anti-inflammatory, and anticancer properties, making it a potential candidate for pharmaceutical applications. Its chemical structure and functional groups contribute to its diverse range of activities, making it an interesting subject for further research and development in the field of natural products chemistry.

6296-57-7

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6296-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6296-57-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6296-57:
(6*6)+(5*2)+(4*9)+(3*6)+(2*5)+(1*7)=117
117 % 10 = 7
So 6296-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H16O6/c1-11(20)24-14-6-4-13-8-15(19(21)25-17(13)10-14)12-5-7-16(22-2)18(9-12)23-3/h4-10H,1-3H3

6296-57-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(3,4-dimethoxyphenyl)-2-oxochromen-7-yl] acetate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6296-57-7 SDS

6296-57-7Relevant academic research and scientific papers

Modified coumarins. 29. Synthesis of structural analogs of natural 6-arylfuro[3,2-g]chromen-7-ones

Garazd,Garazd,Ogorodniichuk,Khilya

experimental part, p. 158 - 163 (2009/12/06)

3-Substituted 6-arylfuro[3,2-g]chromen-7-ones, structural analogs of natural furocoumarins, were synthesized by linear annelation of a furan fragment to a 3-arylcoumarin system.

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