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5,7-Dihydroxy-6-(3-methyl-2-butenyl)-8-(3-methylbutyryl)-4-phenyl-2H-1-benzopyran-2-one is a complex organic compound with a molecular formula of C26H26O6. It is a type of flavonoid, which are naturally occurring compounds found in plants, known for their antioxidant properties and potential health benefits. This specific flavonoid features a benzopyran-2-one core structure, with two hydroxyl groups at the 5 and 7 positions, a 3-methyl-2-butenyl group at the 6 position, and a 3-methylbutyryl group at the 8 position. Additionally, it has a phenyl group at the 4 position, which contributes to its chemical reactivity and potential biological activity. The compound's structure and properties make it a subject of interest in the fields of chemistry, pharmacology, and natural product research.

5224-54-4

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5224-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5224-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5224-54:
(6*5)+(5*2)+(4*2)+(3*4)+(2*5)+(1*4)=74
74 % 10 = 4
So 5224-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C25H26O5/c1-14(2)10-11-17-23(28)21-18(16-8-6-5-7-9-16)13-20(27)30-25(21)22(24(17)29)19(26)12-15(3)4/h5-10,13,15,28-29H,11-12H2,1-4H3

5224-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-dihydroxy-8-(3-methylbutanoyl)-6-(3-methylbut-2-enyl)-4-phenylchromen-2-one

1.2 Other means of identification

Product number -
Other names Mammea A/BA

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:5224-54-4 SDS

5224-54-4Downstream Products

5224-54-4Relevant academic research and scientific papers

Methods and compositions for lowering levels of blood lipids

-

, (2008/06/13)

Disclosed are methods to lower blood cholesterol levels or inhibit ileal apical sodium co-dependent bile acid transport (ASBT) protein using coumarin and anthracene dione derivatives. Pharmaceutical compositions are also disclosed.

Synthesis of Mammea Coumarins. Part 1. The Coumarins of the Mammea A, B, and C Series

Crombie, Leslie,Jones, Raymond C. F.,Palmer, Christopher J.

, p. 317 - 332 (2007/10/02)

The naturally-occuring Mammea coumarins of the 4-phenyl-(mammea A), propyl-(mammea B), and 4-pentyl-(mammea C) series have been prepared by Pechmann condensation of an acylphloroglucinol (3-methylbutyryl-, 2-methylbutyryl-, butyryl-, or 2-methylpropionyl-) with the appropriate β-ketoester to give a mixture of 6- and 8-acyl-5,7-dihydroxycoumarins that could be separated.C-Alkylation with 3-methylbut-2-enyl bromide, or 3,7-dimethylocta-2,6-dienyl chloride, in aqueous potassium hydroxide completed the synthesis of the Mammea coumarins having unmodified prenyl or geranyl substituents; oxidative modification of the prenyl group led to the mammea cyclo E and cyclo F coumarins.Some mammea cyclo D (chromeno) coumarins were synthesized by reaction of acylcoumarins with 1,1-dimethoxy-3-methylbutan-3-ol.

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