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5,7-Dihydroxy-8-(3-methyl-2-butenyl)-6-(2-methylbutyryl)-4-phenyl-2H-1-benzopyran-2-one is a complex organic compound with a molecular formula of C23H24O6. It is a derivative of flavonoids, a class of natural products that are widely found in plants and exhibit various biological activities, such as antioxidant, anti-inflammatory, and anticancer properties. This specific compound is characterized by its unique structure, which includes a benzopyran-2-one core, two hydroxyl groups at the 5 and 7 positions, a 3-methyl-2-butenyl group at the 8 position, a 2-methylbutyryl group at the 6 position, and a phenyl group at the 4 position. Due to its complex structure and potential biological activities, 5,7-Dihydroxy-8-(3-methyl-2-butenyl)-6-(2-methylbutyryl)-4-phenyl-2H-1-benzopyran-2-one may be of interest in the fields of pharmaceuticals, nutraceuticals, and natural product chemistry for further research and development.

7058-70-0

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7058-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7058-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,5 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7058-70:
(6*7)+(5*0)+(4*5)+(3*8)+(2*7)+(1*0)=100
100 % 10 = 0
So 7058-70-0 is a valid CAS Registry Number.

7058-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name mammea A/AB

1.2 Other means of identification

Product number -
Other names Mammea A/AB

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:7058-70-0 SDS

7058-70-0Relevant 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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