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4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxy- is a complex organic compound with the molecular formula C16H14O6. It is a derivative of the benzopyran class, which is a type of heterocyclic compound containing a benzene ring fused to a pyran ring. This specific compound features a 2,3-dihydro structure, indicating that the pyran ring is partially saturated. It has a hydroxyl group at the 5-position, a 3-hydroxy-4-methoxyphenyl group at the 2-position, and a methoxy group at the 7-position. These functional groups contribute to its chemical properties and potential applications in various fields, such as pharmaceuticals or natural product chemistry.

5928-45-0

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5928-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5928-45-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5928-45:
(6*5)+(5*9)+(4*2)+(3*8)+(2*4)+(1*5)=120
120 % 10 = 0
So 5928-45-0 is a valid CAS Registry Number.

5928-45-0SDS

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 5,3'-dihydroxy-7,4'-dimethoxyflavanone

1.2 Other means of identification

Product number -
Other names 5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-7-methoxy-chroman-4-one

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:5928-45-0 SDS

5928-45-0Downstream Products

5928-45-0Relevant academic research and scientific papers

Efficient synthesis of flavanone glucuronides

Boumendjel, Ahcene,Blanc, Madeleine,Williamson, Gary,Barron, Denis

scheme or table, p. 7264 - 7267 (2010/07/05)

The first efficient synthesis of flavanone glucuronides as potential human metabolites is described. The synthetic strategy is based on acetyl protection, followed by a combination of chemical and enzymatic deprotection steps. As an example, the method is

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