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(Z)-2-Methoxy-4-oxo-4-phenyl-but-2-enoic acid methyl ester is a complex organic compound with the chemical formula C12H10O4. It is a derivative of cinnamic acid, featuring a methoxy group at the 2-position, a carbonyl group at the 4-position, and a phenyl ring attached to the 4-position as well. This molecule is characterized by its (Z)-configuration, indicating the geometric arrangement of the double bond, with the phenyl and carbonyl groups on the same side of the double bond. The compound is an ester due to the presence of a methyl group esterified to the carboxylic acid group. It is known for its potential applications in the synthesis of various pharmaceuticals and as a chemical intermediate in the production of certain agrochemicals.

59079-03-7

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59079-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59079-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,7 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59079-03:
(7*5)+(6*9)+(5*0)+(4*7)+(3*9)+(2*0)+(1*3)=147
147 % 10 = 7
So 59079-03-7 is a valid CAS Registry Number.

59079-03-7Downstream Products

59079-03-7Relevant academic research and scientific papers

4-aryl-2,4-dioxobutanoic acids and their derivatives in reactions with diazoalkanes

Zalesov,Kataev,Pulina,Kovylyaeva

, p. 840 - 844 (2007/10/03)

By treating 4-aryl-2,4-dioxobutanoic acids or their alkyl esters with diazomethane alkyl 4-aryl-2-methoxy-4-oxo-2-butenoates and 1-R-3-aroyl-4-methoxy-4-methoxycarbonyl-4,5-dihydropyrazoles were prepared. O-Alkyl derivatives and substituted pyrazoles were

Pyruvic Acid Dimethylhydrazone. A Synthetic Equivalent of the Pyruvic Acid Dianion

Tapia, Ines,Alcazar, Victoria,Moran, Joaquin R.,Caballero, Cruz,Grande, Manuel

, p. 697 - 700 (2007/10/02)

The pyruvic acid dimethyl hydrazone can be easily prepared in ether.This compound, after deprotonation with alkyllithium, forms a strong nucleophile which on tratment with electrophiles and acidic work up yield α-ketoacids, α-hydroxybutenolides or α,γ-diketoacids.

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