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3-(4-Methoxyphenyl)-2H-chromen-7-yl acetate is a chemical compound with the molecular formula C18H14O5. It is a derivative of the flavonoid family, specifically a flavone, and is characterized by the presence of a 4-methoxyphenyl group attached to the 3-position of the chromen-7-yl ring. 3-(4-methoxyphenyl)-2H-chromen-7-yl acetate is known for its potential biological activities, such as antioxidant and anti-inflammatory properties, which are being studied for their potential applications in pharmaceuticals and nutraceuticals. The acetate group at the 7-position further modifies its chemical reactivity and may influence its interaction with biological targets.

10499-10-2

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10499-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10499-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,9 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10499-10:
(7*1)+(6*0)+(5*4)+(4*9)+(3*9)+(2*1)+(1*0)=92
92 % 10 = 2
So 10499-10-2 is a valid CAS Registry Number.

10499-10-2SDS

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 [3-(4-methoxyphenyl)-2H-chromen-7-yl] acetate

1.2 Other means of identification

Product number -
Other names 7-acetoxy-4'-methoxyisoflav-3-ene

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:10499-10-2 SDS

10499-10-2Upstream product

10499-10-2Relevant academic research and scientific papers

Production of isoflavone derivatives

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Page/Page column 10, (2008/06/13)

Methods for the hydrogenation of isoflavones are described which provide access to workable quantities of isoflavan-4-ols, isoflav-3-enes, and isoflavans. The isoflavone derivatives can be obtained in high purity and in near quantitative yields whilst employing pharmaceutically acceptable reagents and solvents.

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