39026-64-7 Usage
Uses
Used in Pharmaceutical Research:
(+/-)-1-Aminocyclopentane-cis-1,2-dicarboxylic acid is used as a research tool for studying the activity of glutamate transporters and their role in synaptic transmission. Its ability to modulate the activity of these transporters makes it a valuable compound in understanding the mechanisms of excitatory neurotransmission.
Used in Neurological Disorder Treatment:
(+/-)-1-Aminocyclopentane-cis-1,2-dicarboxylic acid is being studied for its potential applications in the treatment of neurological disorders. Its influence on glutamate neurotransmission suggests that it may have therapeutic benefits in conditions where glutamate dysregulation is implicated, such as neurodegenerative diseases and certain psychiatric disorders.
Used in Pharmaceutical Compound Synthesis:
(+/-)-1-Aminocyclopentane-cis-1,2-dicarboxylic acid is utilized as a building block in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications in different medical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 39026-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,2 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39026-64:
(7*3)+(6*9)+(5*0)+(4*2)+(3*6)+(2*6)+(1*4)=117
117 % 10 = 7
So 39026-64-7 is a valid CAS Registry Number.
39026-64-7Relevant academic research and scientific papers
Carbamate-directed hydroboration: Enantioselective synthesis of the excitatory amino acid 1-aminocyclopentane-1,3-dicarboxylic acid
Hodgson, David M.,Thompson, Alison J.,Wadman, Sjoerd
, p. 3357 - 3358 (2007/10/03)
Carbamate-directed hydroboration (using BH3) of 1-substituted 3- cyclopentenes 2, 6 and 9 and an enantioselective synthesis of the excitatory amine acid 1-aminocyclopentane-1,3-dicarboxylic acid via carbamate-directed asymmetric hydroboration [90% de, 45% ee using (+)-IpcBH2] of cyclopentene 2 are described.
CHEMOENZYMATIC SYNTHESIS OF CONFORMATIONALLY RIGID GLUTAMIC ACID ANALOGUES
Trigalo, F.,Buisson, D.,Azerad, R.
, p. 6109 - 6112 (2007/10/02)
All stereomers of cyclohexane cyclopentane-derived analogues of glutamic acid have been synthesized from the corresponding 3-keto-cycloalkyl carboxylic acid esters by a combination of microbial steps and standard chemical methods.
