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4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-2,3-dihydro-5,7-dihydroxy- is a complex organic compound with the molecular formula C16H14O6. It is a derivative of chromone, a type of heterocyclic compound with a benzene ring fused to a pyran ring. This specific compound features two hydroxyl groups at the 5 and 7 positions, and a 3,4-dimethoxyphenyl group attached at the 2 position. The dimethoxyphenyl group consists of a benzene ring with two methoxy groups (-OCH3) at the 3 and 4 positions. This chemical structure is significant in the field of organic chemistry and may have potential applications in pharmaceuticals or other industries due to its unique properties and reactivity.

4250-76-4

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4250-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4250-76-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4250-76:
(6*4)+(5*2)+(4*5)+(3*0)+(2*7)+(1*6)=74
74 % 10 = 4
So 4250-76-4 is a valid CAS Registry Number.

4250-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name taxifolin

1.2 Other means of identification

Product number -
Other names 2-(3,4-Dimethoxy-phenyl)-5,7-dihydroxy-chroman-4-on

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:4250-76-4 SDS

4250-76-4Downstream Products

4250-76-4Relevant academic research and scientific papers

Influence of Substrate Binding Residues on the Substrate Scope and Regioselectivity of a Plant O-Methyltransferase against Flavonoids

Tang, Qingyun,Vianney, Yoanes M.,Weisz, Klaus,Grathwol, Christoph W.,Link, Andreas,Bornscheuer, Uwe T.,Pavlidis, Ioannis V.

, p. 3721 - 3727 (2020/06/02)

Methylation of free hydroxyl groups is an important modification for flavonoids. It not only greatly increases absorption and oral bioavailability of flavonoids, but also brings new biological activities. Flavonoid methylation is usually achieved by a specific group of plant O-methyltransferases (OMTs) which typically exhibit high substrate specificity. Here we investigated the effect of several residues in the binding pocket of the Clarkia breweri isoeugenol OMT on the substrate scope and regioselectivity against flavonoids. The mutation T133M, identified as reported in our previous publication, increased the activity of the enzyme against several flavonoids, namely eriodictyol, naringenin, luteolin, quercetin and even the isoflavonoid genistein, while a reduced set of amino acids at positions 322 and 326 affected both, the activity and the regioselectivity of the methyltranferase. On the basis of this work, methylated flavonoids that are rare in nature were produced in high purity.

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