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86654-26-4

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86654-26-4 Usage

General Description

7-Hydroxy-3-prenylcoumarin is a chemical compound that belongs to the coumarin class of compounds. It is a derivative of coumarin and is known for its potential pharmacological properties. The "7-hydroxy" in its name indicates the presence of a hydroxyl group at the 7th position of the coumarin ring, while the "3-prenyl" refers to a prenyl group attached to the coumarin structure. 7-Hydroxy-3-prenylcoumarin has been studied for its various biological activities, including antioxidant, anti-inflammatory, and anti-cancer properties. Its prenyl group may contribute to its biological activities, making it a subject of interest for further research in the development of potential therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 86654-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,5 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86654-26:
(7*8)+(6*6)+(5*6)+(4*5)+(3*4)+(2*2)+(1*6)=164
164 % 10 = 4
So 86654-26-4 is a valid CAS Registry Number.

86654-26-4SDS

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 7-Hydroxy-3-(3-methyl-2-buten-1-yl)-2H-chromen-2-one

1.2 Other means of identification

Product number -
Other names 7-hydroxy-3-prenylcoumarin

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:86654-26-4 SDS

86654-26-4Downstream Products

86654-26-4Relevant articles and documents

Short synthesis of 3-prenylcoumarins by an unusual prenylation

Ramachandra, Marellapudi S.,Subbaraju, Gottumukkala V.

, p. 3723 - 3727 (2007/10/03)

Prenylation of coumarins that have hydroxyl or alkoxyl or halo substitution (1a-1i) using 2-methyl-3-butene-2-ol in the presence of boron trifluoride formed 3-prenylcoumarins (2a-2d). Copyright Taylor & Francis Group, LLC.

Synthesis of Balsamiferone and dl-3-(3,3-Dimethylallyl)marmesin

Swaroop, (KM) Divya,Sharma, R. B.,Kapil, R. S.

, p. 408 (2007/10/02)

The structures of naturally occurring coumarins balsamiferone and 3-(3,3-dimethylallyl)marmesin as 3,6-bis(3-methyl-2-butenyl)-7-hydroxycoumarin and 3-(3-methyl-2-butenyl)-6,7-dihydro-7-(1-hydroxy-1-methylethyl)-2H-furobenzopyran-2-one, respectively have been confirmed by syntheses.

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