41109-94-8 Usage
Description
(2E,4E)-2-cyano-5-phenyl-2,4-pentadienoic acid methyl ester is a chemical compound with a molecular formula of C12H9NO2. It is a methyl ester derivative of pentadienoic acid, specifically a cyanophenylpentadienoic acid. (2E,4E)-2-cyano-5-phenyl-2,4-pentadienoic acid methyl ester is known for its potential applications in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it has been studied for its potential biological activities and pharmacological properties. However, caution should be taken when handling this compound, as it may pose health hazards if not handled properly. Overall, (2E,4E)-2-cyano-5-phenyl-2,4-pentadienoic acid methyl ester is a versatile chemical with diverse potential uses in the field of chemistry and pharmaceuticals.
Uses
Used in Organic Synthesis:
(2E,4E)-2-cyano-5-phenyl-2,4-pentadienoic acid methyl ester is used as a starting material in various chemical reactions for the synthesis of complex organic compounds.
Used in Pharmaceutical Synthesis:
(2E,4E)-2-cyano-5-phenyl-2,4-pentadienoic acid methyl ester is used as a building block in the development of new pharmaceuticals, contributing to the creation of novel drug candidates.
Used in Agrochemical Synthesis:
(2E,4E)-2-cyano-5-phenyl-2,4-pentadienoic acid methyl ester is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides, to improve agricultural productivity.
Used in Fine Chemicals Production:
(2E,4E)-2-cyano-5-phenyl-2,4-pentadienoic acid methyl ester is used as an intermediate in the production of fine chemicals, which are high-purity chemicals used in various industries, including cosmetics, fragrances, and flavorings.
Used in Biological Activity Research:
(2E,4E)-2-cyano-5-phenyl-2,4-pentadienoic acid methyl ester is used as a subject of study in biological activity research to explore its potential pharmacological properties and applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 41109-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,0 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41109-94:
(7*4)+(6*1)+(5*1)+(4*0)+(3*9)+(2*9)+(1*4)=88
88 % 10 = 8
So 41109-94-8 is a valid CAS Registry Number.
41109-94-8Relevant articles and documents
One-Pot Synthesis of γ-Azidobutyronitriles and Their Intramolecular Cycloadditions
Ivanov, Konstantin L.,Tukhtaev, Hamidulla B.,Tukhtaeva, Feruza O.,Bezzubov, Stanislav I.,Melnikov, Mikhail Ya.,Budynina, Ekaterina M.
, p. 3356 - 3373 (2020/09/15)
Efficient gram-scale, one-pot approaches to azidocyanobutyrates and their amidated or decarboxylated derivatives have been developed, starting from commercially available aldehydes and cyanoacetates. These techniques combine (1) Knoevenagel condensation,
Synthesis of (E)-α,β-unsaturated carboxylic esters derivatives from cyanoacetic acid via promiscuous enzyme-promoted cascade esterification/Knoevenagel reaction
Wilk, Monika,Trzepizur, Damian,Koszelewski, Dominik,Brodzka, Anna,Ostaszewski, Ryszard
, (2019/02/25)
A new enzymatic protocol based on lipase-catalyzed cascade toward (E)-α,β-unsaturated carboxylic esters is presented. The proposed methodology consists of elementary organic processes starting from acetals and cyanoacetic acid leading to the formation of desired products in a cascade sequence. The combination of enzyme promiscuous abilities gives a new opportunity to synthesize complex molecules in the one-pot procedure. Results of studies on the influence of an enzyme type, solvent, and temperature on the cascade reaction course are reported. The presented methodology provides meaningful qualities such as significantly simplified process, excellent E-selectivity of obtained products and recycling of a biocatalyst.
Lewis Acid Triggered Vinylcyclopropane-Cyclopentene Rearrangement
Ivanova, Olga A.,Chagarovskiy, Alexey O.,Shumsky, Alexey N.,Krasnobrov, Vasiliy D.,Levina, Irina I.,Trushkov, Igor V.
, p. 543 - 560 (2018/01/27)
We report a mild Lewis acid induced isomerization of donor-acceptor cyclopropanes, containing an alkenyl moiety and diverse electron-withdrawing group(s) at the adjacent positions, into substituted cyclopentenes. We have found that 1,1,2-trisubstituted cy
