158271-95-5 Usage
Description
(R)-1-(2-Hydroxy-1-phenylethyl)-1,5-dihydropyrrol-2-one is a chiral chemical compound characterized by a dihydropyrrol-2-one ring and a phenylethyl group with a hydroxyl substitution. Its unique structure and stereoisomeric configuration contribute to its potential pharmaceutical applications and value as an intermediate in the synthesis of other organic compounds.
Uses
Used in Pharmaceutical Industry:
(R)-1-(2-Hydroxy-1-phenylethyl)-1,5-dihydropyrrol-2-one is used as a pharmaceutical intermediate for the development of new drugs targeting various medical conditions. Its unique chemical structure and chiral nature make it a promising candidate for drug discovery and design.
Used in Organic Synthesis:
(R)-1-(2-Hydroxy-1-phenylethyl)-1,5-dihydropyrrol-2-one is used as a valuable intermediate in the synthesis of other organic compounds, leveraging its distinctive structural features to create novel molecules with potential applications in various fields.
Research and Development:
(R)-1-(2-Hydroxy-1-phenylethyl)-1,5-dihydropyrrol-2-one is the subject of ongoing research to explore its properties and potential uses further. The scientific community continues to investigate its applications in different industries, aiming to unlock its full potential and contribute to advancements in various sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 158271-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,2,7 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 158271-95:
(8*1)+(7*5)+(6*8)+(5*2)+(4*7)+(3*1)+(2*9)+(1*5)=155
155 % 10 = 5
So 158271-95-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO2/c14-9-11(10-5-2-1-3-6-10)13-8-4-7-12(13)15/h1-7,11,14H,8-9H2/t11-/m0/s1
158271-95-5Relevant articles and documents
Asymmetric synthesis of 3-substituted pyrrolidones via α-alkylation of a chiral non-racemic γ-lactam
Baussanne, Isabelle,Travers, Catherine,Royer, Jacques
, p. 797 - 804 (1998)
3-Alkyl pyrrolidones 9 were synthesized in good yield and high diastereoselectivity by α-alkylation of the new chiral non-racemic lactam 8 derived from (R)-(-)-phenylglycinol. After debenzylation and introduction of an electron-withdrawing group, 3-methylpyrrolidone 10 is easily hydrolyzed in a basic medium to produce γ-aminobutyric acid (GABA) analogue 13.