813433-73-7 Usage
Description
(R)-tert-Butyl 2-(2-Methoxy-2-oxoethyl)piperidine-1-carboxylate is a complex chemical compound characterized by its chiral nature and a unique structure that features a piperidine ring and a carboxylate group. The (R)-configuration denotes the direction of the molecule's rotation, which is crucial for its potential applications and interactions. (R)-tert-Butyl 2-(2-Methoxy-2-oxoethyl)piperidine-1-carboxylate holds promise for various uses, particularly in organic synthesis, pharmaceuticals, and as a building block for more complex chemical entities.
Uses
Used in Organic Synthesis:
(R)-tert-Butyl 2-(2-Methoxy-2-oxoethyl)piperidine-1-carboxylate is used as an intermediate in the synthesis of various organic compounds due to its unique structural features and reactivity. Its ability to form new bonds and participate in different chemical reactions makes it a valuable component in creating a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (R)-tert-Butyl 2-(2-Methoxy-2-oxoethyl)piperidine-1-carboxylate is used as a key building block for the development of new drugs. Its chiral nature and specific functional groups can be exploited to create molecules with targeted biological activities, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Research:
(R)-tert-Butyl 2-(2-Methoxy-2-oxoethyl)piperidine-1-carboxylate is also utilized in chemical research as a model compound to study various aspects of chemical reactivity, stereochemistry, and the development of new synthetic methods. Understanding its properties and behavior can contribute to the advancement of chemical science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 813433-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,3,4,3 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 813433-73:
(8*8)+(7*1)+(6*3)+(5*4)+(4*3)+(3*3)+(2*7)+(1*3)=147
147 % 10 = 7
So 813433-73-7 is a valid CAS Registry Number.
813433-73-7Relevant articles and documents
Organocatalytic enantioselective synthesis of quinolizidine alkaloids (+)-myrtine, (-)-lupinine, and (+)-epiepiquinamide
Fustero, Santos,Moscardó, Javier,Sánchez-Roselló, María,Flores, Sonia,Guerola, Marta,Pozo, Carlos Del
, p. 7412 - 7417 (2011/10/09)
The organocatalytic synthesis of quinolizidine alkaloids (+)-myrtine, (-)-lupinine, and (+)-epiepiquinamide is described. It involved, as the key step, an enantioselective intramolecular aza-Michael reaction (IMAMR) catalyzed by J?rgensen catalyst I, affording the common precursor with high enantioselectivity. This compound was subsequently transformed into the three alkaloids in a highly diastereoselective manner.
Chemoenzymatic approach to enantiopure piperidine-based β-amino esters in organic solvents
Liljeblad, Arto,Kavenius, Hanna-Maija,Taehtinen, Petri,Kanerva, Liisa T.
, p. 181 - 191 (2007/10/03)
This research concentrates on the enantioselectivities of lipase-catalysed reactions with methyl esters of 2-piperidylacetic acid and 3-piperidinecarboxylic acid derivatives. N-Acetylated 2-piperidylacetic acid methyl ester displayed good enantioselectivi
Enzymatic resolution of cyclic N-Boc protected β-aminoacids
Pousset, Cyrille,Callens, Roland,Haddad, Mansour,Larcheveque, Marc
, p. 3407 - 3412 (2007/10/03)
Methyl and ethyl esters of N-Boc homoproline, homopipecolic acid and 3-carboxymethyl-morpholine were kinetically resolved by hydrolysis catalysed by Burkholderia cepacia lipase to give the corresponding acids and residual esters in enantiomeric excesses better than 99% (E > 100).
