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4-Hydroxy-2-oxo-1-pyrrolidineacetic acid, also known as 1-Pyrrolidineacetic acid, is a derivative of Oxiracetam, a nootropic compound. It is structurally similar to Piracetam and possesses psychostimulant activity. This molecule is characterized by its potential cognitive-enhancing properties and its ability to stimulate the central nervous system.

77191-37-8

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77191-37-8 Usage

Uses

Used in Pharmaceutical Industry:
4-Hydroxy-2-oxo-1-pyrrolidineacetic acid is used as a nootropic agent for enhancing cognitive functions and memory. Its psychostimulant activity makes it a promising candidate for the development of drugs aimed at improving brain performance and treating cognitive disorders.
Used in Cognitive Enhancement:
4-Hydroxy-2-oxo-1-pyrrolidineacetic acid is used as a cognitive enhancer to improve memory, learning, and focus. Its psychostimulant properties may help in increasing alertness and attention, making it a potential candidate for the treatment of attention deficit disorders and other cognitive impairments.
Used in Research and Development:
In the field of neuroscience and pharmaceutical research, 4-Hydroxy-2-oxo-1-pyrrolidineacetic acid serves as a valuable compound for studying the mechanisms underlying cognitive enhancement and the development of novel therapeutic strategies for neurological and psychiatric conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 77191-37-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,9 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77191-37:
(7*7)+(6*7)+(5*1)+(4*9)+(3*1)+(2*3)+(1*7)=148
148 % 10 = 8
So 77191-37-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO4/c8-4-1-5(9)7(2-4)3-6(10)11/h4,8H,1-3H2,(H,10,11)

77191-37-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-hydroxy-2-oxopyrrolidin-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 4-hydroxy-2-oxopyrrolidin-1-yl-acetic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:77191-37-8 SDS

77191-37-8Relevant academic research and scientific papers

Preparation method and application of 4-hydroxy-2-oxo-1-pyrrolidine acetic acid

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Paragraph 0034-0057, (2021/05/05)

The invention provides a preparation method of 4-hydroxy-2-oxo-1-pyrrolidine acetic acid, and the preparation method comprises the following steps: mixing oxiracetam and a lithium compound to react, so as to obtain the 4-hydroxy-2-oxo-1-pyrrolidine acetic acid. The preparation method provided by the invention is simple to operate, high in yield, high in purity and simple and convenient in post-treatment.

Process for the production of 4-hydroxy-2-oxopyrrolidin-1-yl-acetamide

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, (2008/06/13)

Process for the production of 4-hydroxy-2-oxoyrrolidin-1-yl-acetamide, a cerebrally active pharmaceutical agent. A 4-halo-3-alkoxy-butenoic acid ester is reacted with glycine to new intermediate products of the formula: STR1 There is further by acid hydrolysis of the alkoxy group, subsequent hydrogenation, esterification of the carboxyl function and finally conversion to the end product by reaction with ammonia.

Cyclic GABA-GABOB analogues. IV. Activity on learning and memory.

Banfi,Fonio,Allievi,Pinza,Dorigotti

, p. 16 - 22 (2007/10/02)

A number of N-substituted 4-hydroxy-, 4-acyloxy- and 4-alkoxy-2-pyrrolidinones were examined by a screening method predictive of their activity on cognitive processes. The 1-aminocarbonylmethyl-substituted compounds showed a favorable effect on learning and memory, and among them the most active was the 4-hydroxy derivative, oxiracetam, which had a potency considerably higher than piracetam, used for comparison purposes.

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