52408-04-5 Usage
Uses
Used in Medical and Pharmaceutical Industries:
2,5-Diaminoadipic acid 2HCl is used as a neurological inhibitor for its potential applications in the medical and pharmaceutical industries. It is being studied for its effects on cell signaling and metabolic processes, which could lead to the development of new therapeutic strategies.
Used in Laboratory Applications:
2,5-Diaminoadipic acid 2HCl is used as a stable compound in laboratory settings due to its hydrochloride form. This stability makes it suitable for various research purposes, including the investigation of its biological functions and potential applications in medicine and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 52408-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,0 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52408-04:
(7*5)+(6*2)+(5*4)+(4*0)+(3*8)+(2*0)+(1*4)=95
95 % 10 = 5
So 52408-04-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2O4.2ClH/c7-3(5(9)10)1-2-4(8)6(11)12;;/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12);2*1H
52408-04-5Relevant academic research and scientific papers
Stereospecific synthesis of cyclic hydrazoacetic acids and meso- diaminodicarboxylic acids
Arakawa, Yasushi,Goto, Takahiro,Kawase, Kazuya,Yoshifuji, Shigeyuki
, p. 674 - 680 (2007/10/03)
The hetero Diels-Alder adducts 6a - d derived from azodibenzoyl and cyclic dienes were oxidized by ruthenium tetroxide and transformed into meso- diaminodicarboxylic acids 12a - d via the new cyclic hydrazoacetic acids 9a - d.
Synthesis of (2S,5S)-5-fluoromethylornithine; a potent inhibitor of ornithine aminotransferase
Ducep,Heintzelmann,Jund,Lesur,Schleimer,Zimmermann
, p. 327 - 335 (2007/10/03)
Only one of the four enantiomers of 5-fluoromethylornithine 1 was an irreversible inhibitor of ornithine aminotransferase. The active enantiomer la was synthesized from diaminoadipic acid 2 with a chemical diastereomeric separation and an enantiomeric res
