106874-00-4 Usage
Uses
Used in Pharmaceutical Industry:
(+/-)-3-Formylamino-buttersaeure is used as an intermediate in the synthesis of various bioactive compounds for the development of new pharmaceuticals. Its role in the biosynthesis of GABA makes it a valuable component in the creation of drugs targeting the central nervous system.
Used in Neurological and Psychiatric Research:
(+/-)-3-Formylamino-buttersaeure is used as a research compound to investigate its potential as a therapeutic target for various neurological and psychiatric disorders. Its involvement in the central nervous system and its relationship with GABA suggest that it may have significant implications for the treatment of such conditions.
Used in the Synthesis of GABA Derivatives:
(+/-)-3-Formylamino-buttersaeure is used as a precursor in the synthesis of GABA derivatives, which can be further explored for their potential applications in medicine and neuroscience. The development of GABA-based drugs may lead to new treatments for a range of disorders related to the central nervous system.
Check Digit Verification of cas no
The CAS Registry Mumber 106874-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,7 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106874-00:
(8*1)+(7*0)+(6*6)+(5*8)+(4*7)+(3*4)+(2*0)+(1*0)=124
124 % 10 = 4
So 106874-00-4 is a valid CAS Registry Number.
106874-00-4Relevant academic research and scientific papers
Synthesis of β-amino acids based on oxidative cleavage of dihydropyridone derivatives
Ege, Markus,Wanner, Klaus T.
, p. 3553 - 3556 (2007/10/03)
(Chemical Equation Presented) A new method for the synthesis of β-amino acids based on 2,3-dihydropyridones as starting materials is presented. Conversions of 2,3-dihydropyridones with NaIO4 and subsequently with base gave the corresponding β-amino acids in a one-pot procedure. The reactions have been monitored by 1H NMR indicating that the β-amino acids were formed in quantitative yields mostly. This method appears to be of broad scope, as 2-substituted 2,3-dihydropyridones are easily accessible via N-acyliminium ions generated from 4-methoxypyridine.
