2126899-84-9 Usage
Uses
Used in Pharmaceutical Research:
(E)-4-aminobut-2-enoic acid hydrochloride is used as a research compound for investigating its potential therapeutic effects, particularly in the treatment of neurological disorders and chronic pain. Its unique structure allows for the exploration of its interactions with biological systems and the development of novel treatment strategies.
Used in Drug Synthesis:
(E)-4-aminobut-2-enoic acid hydrochloride is used as a building block in the synthesis of various pharmaceutical compounds. Its versatile structure and reactivity make it a valuable component in the creation of new drugs with potential applications in multiple therapeutic areas.
Used in Laboratory Settings:
The hydrochloride salt form of (E)-4-aminobut-2-enoic acid is used as a water-soluble compound for easier handling and administration in laboratory settings. This enhances the compound's utility in experimental procedures and facilitates its incorporation into research projects.
Check Digit Verification of cas no
The CAS Registry Mumber 2126899-84-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,1,2,6,8,9 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2126899-84:
(9*2)+(8*1)+(7*2)+(6*6)+(5*8)+(4*9)+(3*9)+(2*8)+(1*4)=199
199 % 10 = 9
So 2126899-84-9 is a valid CAS Registry Number.
2126899-84-9Relevant academic research and scientific papers
Forrester, Sean G.,Foster, Joshua,Robert, Sebastien,Salim, Lidya,Desaulniers, Jean-Paul
, p. 4512 - 4513 (2017)
Investigations into the pharmacology of different types of cys-loop GABA receptor have relied for years on the chemical modification of GABA-like compounds. The GABA metabolite GABOB is an attractive molecule to modify due to its convenient chemical structure. In the process of developing new GABA-mimic compounds from GABOB as a starting compound three small molecule GABA derivatives were synthesized using a variety of chemical transformations. Amongst these, a new and reliable method to synthesize TACA (trans-4-aminocrotonic acid) is reported.
