96219-55-5 Usage
Uses
Used in Pharmaceutical Industry:
(S)-2-(2-oxopyrrolidin-1-yl)propanoic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its unique chemical structure and reactivity, contributing to the development of novel therapeutic agents.
Used in Neurological Applications:
(S)-2-(2-oxopyrrolidin-1-yl)propanoic acid is used as a therapeutic agent for neurological disorders such as epilepsy and schizophrenia, due to its role in the regulation of the GABAergic system and its potential to modulate neurotransmission.
Used in Autoimmune Disease Treatment:
(S)-2-(2-oxopyrrolidin-1-yl)propanoic acid is used as a potential treatment for autoimmune diseases, leveraging its anti-inflammatory and immunomodulatory properties to manage the immune response and alleviate disease symptoms.
Used in Agrochemical Industry:
(S)-2-(2-oxopyrrolidin-1-yl)propanoic acid is used as a building block in the synthesis of agrochemicals, taking advantage of its unique chemical properties to create novel compounds for agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 96219-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,1 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96219-55:
(7*9)+(6*6)+(5*2)+(4*1)+(3*9)+(2*5)+(1*5)=155
155 % 10 = 5
So 96219-55-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO3/c1-5(7(10)11)8-4-2-3-6(8)9/h5H,2-4H2,1H3,(H,10,11)/t5-/m0/s1
96219-55-5Relevant academic research and scientific papers
KetoABNO/NOx Cocatalytic Aerobic Oxidation of Aldehydes to Carboxylic Acids and Access to α-Chiral Carboxylic Acids via Sequential Asymmetric Hydroformylation/Oxidation
Miles, Kelsey C.,Abrams, M. Leigh,Landis, Clark R.,Stahl, Shannon S.
supporting information, p. 3590 - 3593 (2016/08/16)
A method for aerobic oxidation of aldehydes to carboxylic acids has been developed using organic nitroxyl and NOx cocatalysts. KetoABNO (9-azabicyclo[3.3.1]nonan-3-one N-oxyl) and NaNO2 were identified as the optimal nitroxyl and NOx sources, respectively. The mildness of the reaction conditions enables sequential asymmetric hydroformylation of alkenes/aerobic aldehyde oxidation to access α-chiral carboxylic acids without racemization. The scope, utility, and limitations of the oxidation method are further evaluated with a series of achiral aldehydes bearing diverse functional groups.
3-Mercaptomethyl-2-oxo-1-pyrrolidine acetic acids and use for hypertension
-
, (2008/06/13)
This invention provides for certain lactam derivatives, their pharmaceutical formulations, and a method of treating hypertension.
