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(E)-2-(3,4-dibenzyloxyphenyl)-4-(α-t-butoxycarbonyl-4-benzyloxybenzylidene)tetronic acid is a complex organic compound characterized by its unique molecular structure. It features a tetronic acid backbone, which is a type of organic compound with a specific arrangement of carbonyl and carboxyl groups. The molecule is adorned with a 3,4-dibenzyloxyphenyl group at the 2-position and an α-t-butoxycarbonyl-4-benzyloxybenzylidene group at the 4-position. The dibenzyloxyphenyl group contributes to the molecule's stability and solubility, while the α-t-butoxycarbonyl-4-benzyloxybenzylidene group introduces a carbonyl group that is protected by a t-butoxycarbonyl (Boc) group, which is a common protecting group in organic synthesis. (E)-2-(3,4-dibenzyloxyphenyl)-4-(α-t-butoxycarbonyl-4-benzyloxybenzylidene)tetronic acid is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and the study of reaction mechanisms. Its structure provides insights into the behavior of such compounds in various chemical reactions and their potential applications in the development of new pharmaceuticals or materials.

93796-47-5

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93796-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93796-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,9 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93796-47:
(7*9)+(6*3)+(5*7)+(4*9)+(3*6)+(2*4)+(1*7)=185
185 % 10 = 5
So 93796-47-5 is a valid CAS Registry Number.

93796-47-5Relevant academic research and scientific papers

Dioxolanones as Synthetic Intermediates. Part 3. Biomimetic Synthesis of Pulvinic Acids

Ramage, Robert,Griffiths, Gareth J.,Sweeney, John N. A.

, p. 1547 - 1553 (2007/10/02)

The reaction of the phosphorane (16) with methyl arylglyoxylates gives 5-(α-methoxycarbonylarylidene)-2,2-pentamethylene-1,3-dioxolan-4-ones which have been treated with the lithium enolates of t-butyl phenylacetic esters to provide a biomimetic synthesis of pulvinic acids.By this method pulvinic acid (2), vulpinic acid (1), and the unsymmetrically substituted compounds, leprapinic acid (3), and xerocomic acid (4) have been prepared; the last named was obtained via an intermediate (28) in which the phenolic groups were protected as benzyl ethers.

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