148345-21-5 Usage
Description
(Z)-ethyl 2-benzoyl-3-(4-Methoxyphenyl)acrylate is a chemical compound with the molecular formula C21H20O4, derived from acrylic acid, featuring a benzoyl group and a 4-methoxyphenyl group. It is a yellow crystalline solid at room temperature, insoluble in water, and soluble in various organic solvents. (Z)-ethyl 2-benzoyl-3-(4-Methoxyphenyl)acrylate is also recognized for its photophysical properties, which render it suitable for light-sensitive applications.
Uses
Used in Organic Synthesis:
(Z)-ethyl 2-benzoyl-3-(4-Methoxyphenyl)acrylate is used as a building block in organic synthesis for the creation of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of a wide range of compounds with different biological activities and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (Z)-ethyl 2-benzoyl-3-(4-Methoxyphenyl)acrylate is used as an intermediate for the synthesis of drugs. Its chemical properties make it a valuable component in the development of new medications with potential therapeutic benefits.
Used in Agrochemical Industry:
(Z)-ethyl 2-benzoyl-3-(4-Methoxyphenyl)acrylate is also utilized as a starting material in the agrochemical industry for the production of pesticides and other agricultural chemicals. Its role in this industry is crucial for enhancing crop protection and yield.
Used in Light-Sensitive Applications:
Due to its photophysical properties, (Z)-ethyl 2-benzoyl-3-(4-Methoxyphenyl)acrylate is used in various light-sensitive applications, such as in the development of materials for photovoltaic cells or in the creation of light-responsive systems in different technological fields.
Check Digit Verification of cas no
The CAS Registry Mumber 148345-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,3,4 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 148345-21:
(8*1)+(7*4)+(6*8)+(5*3)+(4*4)+(3*5)+(2*2)+(1*1)=135
135 % 10 = 5
So 148345-21-5 is a valid CAS Registry Number.
148345-21-5Relevant articles and documents
Enzyme Promiscuity as a Remedy for the Common Problems with Knoevenagel Condensation
Koszelewski, Dominik,Ostaszewski, Ryszard
, p. 10156 - 10164 (2019/07/09)
A new protocol based on lipase-catalyzed tandem reaction toward α,β-enones/enoesters is presented. For the synthesis of the desired products the tandem process based on enzyme-catalyzed hydrolysis and Knoevenagel reaction starting from enol acetates and aldehyde is developed. The relevant impact of the reaction conditions including organic solvent, enzyme type, and temperature on the course of the reaction was revealed. It was shown that controllable release of the active methylene compound from the corresponding enol carboxylate ensured by enzymatic reaction diminishes significantly the formation of the unwanted co-products. Furthermore, this protocol was extended by including a second tandem chemoenzymatic transformation engaging various aldehyde precursors. After a careful optimization of the reaction conditions, the target products were obtained with yields up to 86 % and with excellent E/Z-selectivity.
Synthesis of Ethyl 2-Aminodihydro-5-pyrimidinecarboxylate Derivatives and 3,7-Diethoxycarbonyl-4,6-dihydro-2,4,6,8-tetraaryl-lH-pyrimido[1,2-a]pyrimidines
Milcent, Rene,Malanda, Jean-Claude,Barbier, Geo,Vaissermann, Jacqueline
, p. 329 - 336 (2007/10/03)
Reactions of ethyl 3-aryl-2-benZoylpropenoateS 1 with guanidine and N-alkyl(or benzyl)guanidines have been investigated. Ethyl 2-aminodihydro-5-pyrimidinecarboxylate derivatives 3, 4 or 5 and 3,7-diethoxycarbonyl-4,6-dihydro-2,4,6,8-tetraaryl-lH-pyrimido[
