1114-07-4 Usage
General Description
(3S)-rel-3-Methyl-D-aspartic acid, also known as (3S)-3-Methyl-D-aspartate, is a stereochemical isomer of D-aspartic acid. It is a non-proteinogenic amino acid that modulates the activity of N-methyl-D-aspartate (NMDA) receptors in the central nervous system. (3S)-rel-3-Methyl-D-aspartic acid has been shown to act as a specific agonist at the glycine binding site of the NMDA receptor, leading to an increase in receptor activity. (3S)-rel-3-Methyl-D-aspartic acid has been studied for its potential therapeutic applications in treating neurodegenerative diseases, cognitive disorders, and as a potential neuroprotective agent. It also has implications for research in the field of neuroscience and the understanding of synaptic transmission and memory formation.
Check Digit Verification of cas no
The CAS Registry Mumber 1114-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1114-07:
(6*1)+(5*1)+(4*1)+(3*4)+(2*0)+(1*7)=34
34 % 10 = 4
So 1114-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO4/c1-2(4(7)8)3(6)5(9)10/h2-3H,6H2,1H3,(H,7,8)(H,9,10)/t2-,3+/m0/s1
1114-07-4Relevant articles and documents
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Traynham,J.G.,Williams,V.R.
, p. 2959 - 2961 (1962)
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Organocatalytic synthesis of β-alkylaspartates via β-lactone ring opening
Armstrong, Alan,Geldart, Stephen P.,Jenner, Chloe R.,Scutt, James N.
, p. 8091 - 8094 (2008/02/13)
(Chemical Equation Presented) Cinchona alkaloid-catalyzed reaction of ethyl glyoxylate with substituted ketenes, formed in situ, gives disubstituted β-lactones in moderate yield and high enantiomeric excess. Subsequent azide ring opening, reduction, and e
