147471-19-0 Usage
Description
(E)-3-(4-FLUORO-PHENYL)-BUT-2-ENOIC ACID ETHYL ESTER, also known as (E)-3-(4-fluorophenyl)but-2-enoic acid ethyl ester, is a chemical compound that belongs to the class of butenoic acid esters. It is derived from the ethyl ester of (E)-3-(4-fluoro-phenyl)-but-2-enoic acid, which is a compound used in organic synthesis and pharmaceutical research. This chemical is characterized by its fluorophenyl group and butenoic acid ester structure, which contribute to its potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(E)-3-(4-FLUORO-PHENYL)-BUT-2-ENOIC ACID ETHYL ESTER is used as a precursor for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a valuable building block in the development of new drugs, particularly those targeting specific biological processes or receptors.
Used in Research and Development:
In the field of research and development, (E)-3-(4-FLUORO-PHENYL)-BUT-2-ENOIC ACID ETHYL ESTER serves as a reagent or intermediate for the synthesis of other organic compounds. Its versatility in chemical reactions makes it a useful tool for scientists and researchers working on the development of novel chemical entities and understanding complex biological mechanisms.
Used in Organic Synthesis:
(E)-3-(4-FLUORO-PHENYL)-BUT-2-ENOIC ACID ETHYL ESTER is also utilized in organic synthesis, where it can be employed to create a wide range of chemical products. Its fluorophenyl group and butenoic acid ester structure provide opportunities for further functionalization and modification, making it a valuable component in the synthesis of various organic compounds with potential applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 147471-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,4,7 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 147471-19:
(8*1)+(7*4)+(6*7)+(5*4)+(4*7)+(3*1)+(2*1)+(1*9)=140
140 % 10 = 0
So 147471-19-0 is a valid CAS Registry Number.
147471-19-0Relevant articles and documents
Copper-Photocatalyzed Contra-Thermodynamic Isomerization of Polarized Alkenes
Bouillon, Jean-Philippe,Brégent, Thibaud,Poisson, Thomas
supporting information, p. 7688 - 7693 (2020/10/09)
The contra-thermodynamic isomerization of α- and β-substituted cinnamate derivatives catalyzed by the Cu(OAc)2/rac-BINAP complex under blue light irradiation is reported. The use of an oxazolidinone template, which favored the complexation of the copper catalyst to the substrate, allowed the E → Z isomerization of the catalytically formed chromophore under simple and robust reaction conditions in good to excellent ratios. The mechanism of this process based on the transient formation of a chromophore was also studied.
Selective Synthesis of Z-Cinnamyl Ethers and Cinnamyl Alcohols through Visible Light-Promoted Photocatalytic E to Z Isomerization
Li, Hengchao,Chen, Hang,Zhou, Yang,Huang, Jin,Yi, Jundan,Zhao, Hongcai,Wang, Wei,Jing, Linhai
supporting information, p. 555 - 559 (2020/02/05)
A photocatalytic E to Z isomerization of alkenes using an iridium photosensitizer under mild reaction conditions is disclosed. This method provides scalable and efficient access to Z-cinnamyl ether and allylic alcohol derivatives in high yields with excellent stereoselectivity. Importantly, this method also provides a powerful strategy for the selective synthesis of Z-magnolol and honokiol derivatives possessing potential biological activity.
The synthesis of non-racemic β-alkyl-β-aryl-disubstituted allyl alcohols and their transformation into allylamines and amino acids bearing a quaternary stereocenter
Narczyk, Aleksandra,Pieczykolan, Micha?,Stecko, Sebastian
supporting information, p. 3921 - 3946 (2018/06/08)
A synthesis of non-racemic β-alkyl-β-aryl allyl alcohols and their transformation into allylamines bearing a quaternary stereogenic center is reported. The allyl alcohols were prepared either by Cu-catalyzed enantioselective reduction of enones or by sequ
