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(5S)-(+)-2-Oxopyrrolidine-5-acetic Acid, also known as L-pipecolic acid, is a chiral chemical compound belonging to the class of pyrrolidines. It is characterized by its specific stereochemistry, denoted by the (5S)-(+) notation. This molecule plays a significant role in various biological processes in the human body, including the metabolism of lysine and the biosynthesis of hydroxyproline. Additionally, it functions as a neurotransmitter and has been studied for its potential therapeutic properties, such as neuroprotection and modulation of the immune response.

61884-75-1

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61884-75-1 Usage

Uses

Used in Pharmaceutical Industry:
(5S)-(+)-2-Oxopyrrolidine-5-acetic Acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Neuroprotection Research:
As a neurotransmitter, (5S)-(+)-2-Oxopyrrolidine-5-acetic Acid is used in research aimed at understanding its role in neuroprotection. Studies are conducted to explore its potential to protect neurons from damage and degeneration, which could lead to the development of treatments for neurodegenerative diseases.
Used in Immunomodulation Research:
(5S)-(+)-2-Oxopyrrolidine-5-acetic Acid is also used in research focused on its ability to modulate the immune response. This involves investigating how it can influence the immune system to potentially treat autoimmune diseases or enhance the body's defense against infections.
Used in Metabolic Studies:
In the field of metabolism, (5S)-(+)-2-Oxopyrrolidine-5-acetic Acid is used to study its involvement in the metabolism of lysine and the biosynthesis of hydroxyproline. Understanding its role in these processes can provide insights into the development of treatments for metabolic disorders and other related health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 61884-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,8 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61884-75:
(7*6)+(6*1)+(5*8)+(4*8)+(3*4)+(2*7)+(1*5)=151
151 % 10 = 1
So 61884-75-1 is a valid CAS Registry Number.

61884-75-1Relevant academic research and scientific papers

SYNTHESIS OF 2-OXA AND 2-AZA ANALOGS OF PYRROLIZIDINE-3,5-DIONES (LUKES-SORM DILACTAM)

Nagasaka, Tatsuo,Hakamada, Rie,Kunii, Shin-ichi,Hamaguchi, Fumiko

, p. 619 - 630 (2007/10/02)

The synthesis of 2-oxa and 2-aza analogs of pyrrolizidine-3,5-dione (Lukes-Sorm dilactam), which has amnesia reversal activity, is reported.Optically active (+)-2-oxa and (+)-2-aza analogs and racemic 2-aza analog and its 1-methoxycarbonyl derivatives were prepared from (-)-S-pyroglutamic acid and succinimide, respectively.

Stereoselective Nucleophilic Additions to the Carbon-Nitrogen Double Bond. 3. Chiral Acyliminium Ions

Polniaszek, Richard P.,Belmont, Stephen E.,Alvarez, Ramon

, p. 215 - 223 (2007/10/02)

(S)-(-)-α-Phenethylamine (3), (S)-(-)-1-(2-chlorophenyl)ethylamine (4), (S)-(-)-1-(2,6-dichlorophenyl)ethylamine (5), and (S)-(-)-1-(2,3,4,5,6-pentachlorophenyl)ethylamine (6) have been incorporated into acyliminium ions of structural type 1 and 2.Five-me

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