25441-65-0 Usage
Uses
Used in Pharmaceutical Industry:
(S)-2-AMINO-3-(4-METHOXY-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER is used as a potential therapeutic agent for its possible effects on the central nervous system, respiratory system, and metabolic processes. (S)-2-AMINO-3-(4-METHOXY-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER's interactions with specific biological targets may contribute to its pharmacological properties, making it a candidate for further research and development in the pharmaceutical field.
Used in Medical Research:
In the medical research field, (S)-2-AMINO-3-(4-METHOXY-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER is used as a subject of study to explore its potential biological activities and pharmacological properties. Further investigation is necessary to fully understand its capabilities and how it may be utilized in the development of new treatments or therapies for various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 25441-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,4 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25441-65:
(7*2)+(6*5)+(5*4)+(4*4)+(3*1)+(2*6)+(1*5)=100
100 % 10 = 0
So 25441-65-0 is a valid CAS Registry Number.
25441-65-0Relevant academic research and scientific papers
Chiral azo compounds: Enantioselective synthesis and transformations into β-amino alcohols and α-amino acids with a quaternary stereocenter
Dietz, Friedrich R.,Prechter, Agnes,Gr?ger, Harald,Heinrich, Markus R.
, p. 655 - 657 (2011/03/21)
Taking advantage of radical carboaminations producing azo compounds, a new chemo-enzymatic approach to enantiomerically enriched azo alcohols, β-amino alcohols and non-natural (aromatic) amino acids with a quaternary stereocenter is reported.
Transforming natural amino acids into α-alkyl-substituted amino acids with the help of the HOF·CH3CN complex
Harel, Tal,Rozen, Shlomo
, p. 6500 - 6503 (2008/02/10)
(Chemical Equation Presented) α-Alkyl amino acids can be efficiently prepared in high yields from the respective amino acids themselves. The key step is the oxidation of the amine function to create the corresponding α-nitro acid in a fast and very high yield reaction followed by phase-transfer alkylation and finally reduction to the desired α-alkyl amino acid. Several such acids containing aromatic rings or additional carboxylic groups and acids with steric hindrance at the α-position are suitable substrates. Several alkyl halides were examined as alkylating agents.
