158271-95-5 Usage
General Description
(R)-1-(2-Hydroxy-1-phenylethyl)-1,5-dihydropyrrol-2-one is a chemical compound with a unique structure that includes a dihydropyrrol-2-one ring and a phenylethyl group with a hydroxyl substitution. It is a chiral molecule with a specific stereoisomeric configuration. (R)-1-(2-Hydroxy-1-phenylethyl)-1,5-dihydropyrrol-2-one has potential pharmaceutical applications, particularly in the development of new drugs for the treatment of various medical conditions. Additionally, its unique chemical structure makes it a valuable intermediate for the synthesis of other organic compounds. Research on the properties and potential uses of (R)-1-(2-Hydroxy-1-phenylethyl)-1,5-dihydropyrrol-2-one is ongoing, and it continues to be the subject of scientific interest and exploration.
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.
