114079-50-4 Usage
Uses
Used in Chemical Synthesis:
2-Methylamino-propionic acid methyl ester hydrochloride is used as a reagent in chemical synthesis for its ability to facilitate the formation of new compounds through various chemical reactions. Its stability and water solubility make it an ideal candidate for use in a wide range of synthesis processes.
Used in Pharmaceutical Research:
In pharmaceutical research, 2-Methylamino-propionic acid methyl ester hydrochloride is used as a reagent to explore its potential in the development of new drugs. Its unique chemical properties allow researchers to investigate its interactions with biological systems and its potential therapeutic effects.
Used as a Precursor in Pharmaceutical Production:
2-Methylamino-propionic acid methyl ester hydrochloride is used as a precursor in the production of other pharmaceutical compounds. Its role in the synthesis of various drugs makes it an essential component in the development of new medications and therapies.
Used in Industrial Laboratories:
This chemical compound is commonly used in industrial laboratories for research purposes. Its versatility and stability make it a valuable tool for scientists and researchers working in the fields of chemistry and pharmaceuticals, enabling them to conduct experiments and develop new applications for 2-Methylamino-propionic acid methyl ester hydrochloride.
Check Digit Verification of cas no
The CAS Registry Mumber 114079-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,7 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114079-50:
(8*1)+(7*1)+(6*4)+(5*0)+(4*7)+(3*9)+(2*5)+(1*0)=104
104 % 10 = 4
So 114079-50-4 is a valid CAS Registry Number.
114079-50-4Relevant academic research and scientific papers
Fluorogenic peptide substrates for serine and threonine phosphatases
Xue, Fengtian,Seto, Christopher T.
supporting information; experimental part, p. 1936 - 1939 (2010/07/06)
Figure presented A new fluorescent assay for Ser/Thr protein phosphatases has been developed. Hydrolysis of a phosphoSer residue liberates the Ser hydroxyl group, which induces a cyclization reaction on the N-terminal carbamate and releases a fluorescent reporter. Sequence selectivity is observed using several peptide substrates against alkaline phosphatase (ALP), bacteriophage protein phosphatase (-PPase), and vaccinia H1 related phosphatase (VHR). These studies suggest that the assay could be a useful tool for profiling the substrate specificities of medicinally important phosphatases.
