124957-47-7 Usage
Uses
Used in Pharmaceutical Drug Development:
(E)-methyl 2-((isopropylamino)methyl)-3-phenylacrylate is used as a key intermediate in the synthesis of pharmaceutical drugs for its potential to facilitate the creation of diverse nitrogen-containing compounds. Its unique reactivity and structural features make it a promising candidate for developing new medications with novel mechanisms of action.
Used in Agrochemical Development:
In the agrochemical industry, (E)-methyl 2-((isopropylamino)methyl)-3-phenylacrylate is used as a chemical building block for the development of new agrochemicals. Its structural properties allow for the design of compounds with specific pesticidal or herbicidal activities, contributing to more effective and targeted agricultural solutions.
Used in Organic Synthesis:
(E)-methyl 2-((isopropylamino)methyl)-3-phenylacrylate is employed as a versatile reagent in organic synthesis, particularly for the creation of complex molecular structures. Its phenyl and acrylate groups, along with the isopropylamino moiety, provide a foundation for various chemical transformations, enabling the synthesis of a wide range of organic compounds.
Used in Medicinal Chemistry Research:
(E)-methyl 2-((isopropylamino)methyl)-3-phenylacrylate is utilized as a valuable research tool in medicinal chemistry, where it can be used to study the structure-activity relationships of potential drug candidates. Its unique structural features allow researchers to probe the interactions between molecules and biological targets, aiding in the design of more effective therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 124957-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,9,5 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124957-47:
(8*1)+(7*2)+(6*4)+(5*9)+(4*5)+(3*7)+(2*4)+(1*7)=147
147 % 10 = 7
So 124957-47-7 is a valid CAS Registry Number.
124957-47-7Relevant academic research and scientific papers
Stereoselective Synthesis of 3-Carboxy-4,5-dihydropyrroles via an Intramolecular Iminium Ion Cyclization Reaction
Xiang, Jinbao,Xie, Hongxiang,Li, Zhuo,Dang, Qun,Bai, Xu
supporting information, p. 3818 - 3821 (2015/08/18)
An efficient and practical method has been developed for the synthesis of trans-4,5-disubstituted 3-carboxy-4,5-dihydropyrroles via an intramolecular iminium ion cyclization reaction of readily accessible Baylis-Hillman derivatives and aldehydes in modera
A convenient route to β-amino propionic acid derivatives
Kundu, Mrinal K.,Bhat, Sujata V.
, p. 93 - 101 (2007/10/03)
A general convenient procedure for the synthesis of β-amino-propionic acid derivatives from Baylis-Hillman adducts is reported.
115. α-Methylidene-and α-alkylidene-β-lactams from nonproteinogenic amino acids
Buchholz, Rainer,Hoffmann, H. Martin R.
, p. 1213 - 1220 (2015/01/08)
Treatment of methyl 2-(l-hydroxyalkyl)prop-2-enoates1 with conc. HBr solution afforded methyl (Z)-2-(bromomethyl)alk-2-enoates 2, which were transformed regioselectively into N-substituted methyl (E)-2-(aminomethyl)alk-2-enoates 3 (SN2 reaction
Preparation d'amines allyliques a partir d'acyloxy-3 methylene-2 propionates de methyle substitues en 3 par un groupement aromatique ou heteroaromatique
Foucaud, Andre,Guemmout, Farid El
, p. 403 - 408 (2007/10/02)
The reaction of substituted methyl 3-acetoxy 2-methylene propionates 2 with aliphatic amines gives allylic amines.The E configuration is predominant.The reaction of esters 2 with aniline does not give allylic amines.These amines are prepared by rearrangement of the carbamates which are obtained by the reaction of phenyl isocyanate with methyl 3-hydroxy 2-methylene propionates 1.The primary allylic amines are prepared through the reduction of azides 11.
