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5,6-Dimethyl-7H-furo[3,2-g]chromen-7-one is a naturally occurring chemical compound with the molecular formula C13H10O4. It belongs to the class of furochromenones, which are heterocyclic compounds derived from the fusion of a furan ring with a chromenone. This specific compound is characterized by the presence of two methyl groups at the 5 and 6 positions of the furochromenone structure. It is known for its potential biological activities, such as antioxidant and anti-inflammatory properties, and is found in certain plants, which may contribute to their medicinal value. The compound's structure and properties make it a subject of interest in the field of natural product chemistry and pharmacology.

7469-12-7

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7469-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7469-12-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7469-12:
(6*7)+(5*4)+(4*6)+(3*9)+(2*1)+(1*2)=117
117 % 10 = 7
So 7469-12-7 is a valid CAS Registry Number.

7469-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dimethylfuro[3,2-g]chromen-7-one

1.2 Other means of identification

Product number -
Other names 3,4-dimethylpsoralen

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:7469-12-7 SDS

7469-12-7Downstream Products

7469-12-7Relevant academic research and scientific papers

A convenient synthesis of psoralens

Chimichi, Stefano,Boccalini, Marco,Cosimelli, Barbara,Viola, Giampietro,Vedaldi, Daniela,Dall'Acqua, Francesco

, p. 4859 - 4863 (2007/10/03)

An efficient synthesis (yields >70%) of linear 7H-furo[3,2-g]chromen-7-one derivatives (psoralens or furocoumarins) has been carried out starting from ring-substituted 2-(coumarin-7-yl)oxyaldehydes; moreover, the phototoxicity of these compounds has been tested on a cultured cell line of murine fibroblast.

Synthesis of 3,4-Dimethylpsoralene, Angelicin and Their Derivatives

Ahluwalia, V. K.,Khanduri, C. H.,Sharma, N. D.

, p. 748 - 751 (2007/10/02)

7-Hydroxy-3,4-dimethyl-2H-1-benzopyran-2-one (1) on alkylation followed by Claisen migration of the intermediate allyloxycoumarin 2 gives 8-allyl-7-hydroxy-3,4-dimethyl-2H-1-benzopyran-2-one (3) which on oxidation with OsO4-KIO4 and subsequent cyclodehydration with PPA yields 6,7-dimethyl-5H-furobenzopyran-5-one (4).However, the allylcoumarin 3 on cyclisation with sulphuric acid followed by DDQ affords 2,6,7-trimethyl-5H-furobenzopyran-5-one (6).The isomeric 5,6-dimethyl-7H-furobenzopyran-7-one (10) and 2,5,6-trimethyl-7H-furobenzopyran-7-one (12) have been synthesised starting from 7-hydroxy-8-iodo-3,4-dimethyl-2H-1-benzopyran-2-one (7).Similarly, 5,6,9-trimethyl-7H-furobenzopyran-7-one (16) and 2,5,6,9-tetramethyl-7H-furobenzopyran-7-one (18), and 4,8,9-trimethyl-7H-furobenzopyran-7-one (22) and 2,4,8,9-tetramethyl-7H-furobenzopyran-7-one (24) have been synthesised starting from the appropriate benzopyran-2-ones (13 and 19).

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