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5-Benzylidene-2-phenyl-1,3-dioxane-4,6-dione is a complex organic compound characterized by its unique molecular structure. It is a derivative of 1,3-dioxane, featuring a benzylidene group at the 5-position and a phenyl group at the 2-position. The compound is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates due to its reactive ketone and dioxane rings. Its chemical formula is C16H12O4, and it has a molecular weight of 268.26 g/mol. The compound's structure allows for various functional group modifications, making it a versatile building block in organic chemistry.

4379-29-7

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4379-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4379-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4379-29:
(6*4)+(5*3)+(4*7)+(3*9)+(2*2)+(1*9)=107
107 % 10 = 7
So 4379-29-7 is a valid CAS Registry Number.

4379-29-7Downstream Products

4379-29-7Relevant academic research and scientific papers

Some unusual reactions of Meldrum's acid. Synthesis of cinnamic acids, coumarins and 2-benzyl-1-indanone

Mahulikar,Mane

, p. 12 - 14 (2007/10/03)

The use of Meldrum's acid (1) in the synthesis of the substituted cinnamic acid 3 and malonic acid 4, the coumarins 8 and 9, and of 2-benzyl-1-indanone (13), is reported. The structure of benzylidene benzalmalonate is corrected to 14.

Synthesis of 5-alkylidene-1,3-dioxane-4,6-diones, an easily accessible family of axially chiral alkenes: Preparation in non-racemic form and platinum binding studies

Casadesus, Meritxell,Coogan, Michael P.,Ooi, Li-Ling

, p. 3822 - 3830 (2008/09/18)

A general synthetic route to 5-alkylidene-1,3-dioxane-4,6-diones, which are a family of axially chiral alkenes, is described. Conformational issues are explored and the platinum-binding properties of these species are discussed. That these alkenes exist as stable enantiomers is established by their partial kinetic resolution upon reaction with cysteine. The Royal Society of Chemistry 2006.

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