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3-(3,4-dimethoxy-phenyl)-7-methoxy-chroman is a complex organic compound characterized by its unique molecular structure. It features a chroman ring system, which is a type of chromone with a saturated ring. The chroman ring is substituted with a 3,4-dimethoxy-phenyl group at the 3-position and a methoxy group at the 7-position. 3-(3,4-dimethoxy-phenyl)-7-methoxy-chroman is known for its potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs and other bioactive molecules. Its specific properties and reactivity are influenced by the presence of the electron-donating methoxy groups, which can affect its stability, solubility, and interaction with other molecules.

4278-54-0

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4278-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4278-54-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4278-54:
(6*4)+(5*2)+(4*7)+(3*8)+(2*5)+(1*4)=100
100 % 10 = 0
So 4278-54-0 is a valid CAS Registry Number.

4278-54-0Upstream product

4278-54-0Downstream Products

4278-54-0Relevant academic research and scientific papers

o-Quinone methide based approach to isoflavans: application to the total syntheses of equol, 3′-hydroxyequol and vestitol

Gharpure, Santosh J.,Sathiyanarayanan,Jonnalagadda, Prasad

, p. 2974 - 2978 (2008/09/20)

A concise strategy is developed for the synthesis of isoflavans employing a Diels-Alder reaction between o-quinone methides and aryl-substituted enol ethers followed by reductive cleavage of the acetal group. The method is extended towards the total syntheses of equol, 3′-hydroxyequol and vestitol.

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