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4-Propyl-5,7-dihydroxy-6-(3-methyl-2-butenyl)-8-butyryl-2H-1-benzopyran-2-one is a complex organic compound with a molecular formula of C21H26O6. It is a type of flavonoid, which are naturally occurring compounds found in plants, known for their antioxidant properties. This specific compound is characterized by a benzopyran-2-one core structure, with a propyl group at the 4-position, two hydroxyl groups at the 5 and 7 positions, a 3-methyl-2-butenyl group at the 6-position, and a butyryl group at the 8-position. These structural features contribute to its potential biological activities, which may include antioxidant, anti-inflammatory, and other health-promoting effects. The compound's complex structure also suggests that it could be involved in various biochemical pathways within plants, potentially playing a role in defense mechanisms or pigmentation.

5085-54-1

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5085-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5085-54-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,8 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5085-54:
(6*5)+(5*0)+(4*8)+(3*5)+(2*5)+(1*4)=91
91 % 10 = 1
So 5085-54-1 is a valid CAS Registry Number.

5085-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name mammea B/BC

1.2 Other means of identification

Product number -
Other names 8-Butyryl-5,7-dihydroxy-6-(3-methyl-but-2-enyl)-4-propyl-cumarin

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:5085-54-1 SDS

5085-54-1Relevant academic research and scientific papers

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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