61884-75-1 Usage
General Description
(5S)-(+)-2-Oxopyrrolidine-5-acetic Acid is a chemical compound that belongs to the class of pyrrolidines. It is a chiral molecule with a specific stereochemistry, denoted by the (5S)-(+) notation. (5S)-(+)-2-Oxopyrrolidine-5-acetic Acid is also known as L-pipecolic acid, and it plays a role in various biological processes in the human body. L-pipecolic acid is a natural amino acid derivative, and it is involved in the metabolism of lysine as well as in the biosynthesis of hydroxyproline. It also acts as a neurotransmitter and has been studied for its potential therapeutic properties, including its role in neuroprotection and its ability to modulate the immune response. Overall, (5S)-(+)-2-Oxopyrrolidine-5-acetic Acid is an important molecule with diverse physiological functions.
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 articles and documents
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
