4931-68-4 Usage
Description
BUTYL (S)-(-)-2-PYRROLIDONE-5-CARBOXYLATE, also known as Butyl Pyroglutamate, is a derivative of L-Glutamic Acid, which is an important neurotransmitter that plays a key role in long-term potentiation and is crucial for learning and memory. BUTYL (S)-(-)-2-PYRROLIDONE-5-CARBOXYLATE is characterized by its potential applications in various industries due to its unique properties.
Uses
Used in Pharmaceutical Industry:
BUTYL (S)-(-)-2-PYRROLIDONE-5-CARBOXYLATE is used as a pharmaceutical compound for its potential role in enhancing learning and memory. Its connection to L-Glutamic Acid, a key neurotransmitter, suggests that it may have applications in the development of treatments for cognitive disorders and improving overall brain function.
Used in Research Applications:
In the field of neuroscience research, BUTYL (S)-(-)-2-PYRROLIDONE-5-CARBOXYLATE serves as a valuable tool for studying the mechanisms of long-term potentiation and the role of L-Glutamic Acid in learning and memory processes. BUTYL (S)-(-)-2-PYRROLIDONE-5-CARBOXYLATE can be utilized in experimental setups to better understand the intricacies of neurotransmission and cognitive function.
Used in Drug Development:
BUTYL (S)-(-)-2-PYRROLIDONE-5-CARBOXYLATE may be employed as a starting point or a structural component in the development of new drugs targeting cognitive enhancement or the treatment of neurological disorders. Its relationship with L-Glutamic Acid and its potential effects on learning and memory make it an interesting candidate for further exploration in drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 4931-68-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4931-68:
(6*4)+(5*9)+(4*3)+(3*1)+(2*6)+(1*8)=104
104 % 10 = 4
So 4931-68-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO3/c1-2-3-6-13-9(12)7-4-5-8(11)10-7/h7H,2-6H2,1H3,(H,10,11)/t7-/m0/s1
4931-68-4Relevant articles and documents
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Segel
, p. 851 (1952)
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Acylase I in the alcoholysis of α-substituted dicarboxylic acid esters and derivatives: Enantio- and regioselectivity
Liljeblad, Arto,Lindborg, Jutta,Kanerva, Liisa T.
, p. 3957 - 3966 (2007/10/03)
Enantio- and regioselective butanolyses of α-substituted dimethyl succinates (substituents: Me-, MeO2CCH2-, NH2-, AcHN-, PrCOHN-, HO-, MeO-, PrO-, AcO-, PrCO2-, HepCO2-, Cl- and Br-) and glutarates (substituents: PrCONH- and CbzNH-) and that of methyl pyroglutamate with acylase I enzymes have been studied. Acylase I-catalyzed reactions were totally regioselective proceeding exclusively at the sterically more hindered methyl ester group α to the substituent. High enantioselectivities (E from 50 to >>100) were observed only for the substrates containing CONH functionality in the substituent although the C-N bond was unreactive. The nature of the substituent influenced which of the two enantiomers reacted faster. Copyright (C) 2000 Elsevier Science Ltd.
Studies on pyrrolidones. An improved synthesis of pyroglutamoyl chloride
Rigo,El Ghammarti,Gautret,Couturier
, p. 2597 - 2607 (2007/10/02)
The reaction of trimethylsilyl pyroglutamate with oxalyl chloride at room temperature easily yields pyroglutamoyl chloride. This unstable compound, obtained with difficulty by other methods, is suitable for the preparation of pyroglutamic esters and amides.
