622833-72-1 Usage
Uses
Used in Pharmaceutical Industry:
(R)-1-(4-methoxybenzyl)-3-(benzyloxy)pyrrolidine-2,5-dione is used as a potential pharmaceutical compound for its possible applications in drug development. Its unique structure may offer properties that can be harnessed to create new medications or improve existing ones.
Used in Drug Synthesis:
In the field of drug synthesis, (R)-1-(4-methoxybenzyl)-3-(benzyloxy)pyrrolidine-2,5-dione serves as a key intermediate or building block for the creation of more complex molecules with specific therapeutic effects. Its structural features can be manipulated to design novel drugs with improved efficacy and reduced side effects.
Used in Medicinal Chemistry Research:
(R)-1-(4-methoxybenzyl)-3-(benzyloxy)pyrrolidine-2,5-dione is utilized as a subject of study in medicinal chemistry research to understand its interactions with biological targets and its potential role in treating various diseases. (R)-1-(4-methoxybenzyl)-3-(benzyloxy)pyrrolidine-2,5-dione's structure-activity relationship can be investigated to optimize its pharmacological properties and develop more effective therapeutic agents.
Used in Drug Delivery Systems:
(R)-1-(4-methoxybenzyl)-3-(benzyloxy)pyrrolidine-2,5-dione may be employed in the development of innovative drug delivery systems, such as nanoparticles or liposomes, to enhance the bioavailability, targeting, and overall efficacy of the compound. These systems can help overcome limitations associated with traditional drug administration methods and improve patient outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 622833-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,2,8,3 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 622833-72:
(8*6)+(7*2)+(6*2)+(5*8)+(4*3)+(3*3)+(2*7)+(1*2)=151
151 % 10 = 1
So 622833-72-1 is a valid CAS Registry Number.
622833-72-1Relevant academic research and scientific papers
Intramolecular Mannich and Michael Annulation Reactions of Lactam Derivatives Bearing Enals to Afford Bicyclic N-Heterocycles
Krishna, Yarkali,Shilpa, Kola,Tanaka, Fujie
, p. 8444 - 8448 (2019/10/16)
Acid-catalyzed intramolecular vinylogous Mannich reactions and intramolecular Michael reactions affording pyrrolizinone-fused N-heterocycles from hydroxylactam derivatives bearing enals have been developed. Depending on the substituent on the hydroxylacta
Synthesis of polyhydroxylated quinolizidine and indolizidine scaffolds from sugar-derived lactams via a one-pot reduction/Mannich/Michael sequence
Szczesniak, Piotr,Stecko, Sebastian,Maziarz, Elzbieta,Staszewska-Krajewska, Olga,Furman, Bartlomiej
, p. 10487 - 10503 (2015/02/19)
A direct approach to the synthesis of indolizidine and quinolizidine scaffolds of iminosugars is described. The presented strategy is based on a one-pot sugar lactam reduction with Schwartz's reagent followed by a diastereoselective Mannich/Michael tandem reaction of the resulting sugar imine with Danishefsky's diene. The stereochemical course of the investigated reaction has been explained in detail. The obtained bicyclic products are attractive building blocks for the synthesis of various naturally occurring polyhydroxylated alkaloids and their derivatives.
