1217624-82-2 Usage
Uses
Used in Pharmaceutical Research:
(2R)-2-[(tert-butoxy)carbonyl]amino-4-(4-fluorophenyl)butanoic acid is used as a key intermediate in pharmaceutical research for the development of drugs targeting various medical conditions. Its unique structure and functional groups contribute to its potential as a building block for novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, (2R)-2-[(tert-butoxy)carbonyl]amino-4-(4-fluorophenyl)butanoic acid serves as a versatile reactant or precursor for the synthesis of more complex organic molecules. Its presence of a fluorophenyl group and a tert-butoxycarbonyl amino group allows for a range of chemical reactions, making it a valuable component in the creation of new compounds.
Further Research and Investigation:
The specific properties and potential uses of (2R)-2-[(tert-butoxy)carbonyl]amino-4-(4-fluorophenyl)butanoic acid necessitate additional research and investigation. This will help in uncovering its full potential and exploring new applications across different industries, particularly in the development of innovative pharmaceuticals and advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1217624-82-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,6,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1217624-82:
(9*1)+(8*2)+(7*1)+(6*7)+(5*6)+(4*2)+(3*4)+(2*8)+(1*2)=142
142 % 10 = 2
So 1217624-82-2 is a valid CAS Registry Number.
1217624-82-2Relevant academic research and scientific papers
FACTOR XIIA INHIBITORS
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Paragraph 00408; 00411, (2019/10/19)
This invention relates to compoundsof formula (I)and methods of treatment using the compounds. The invention also relates to processes and methods for producing the compounds of the invention. The compounds of the invention are modulators of Factor XII (e.g. Factor XIIa). In particular, the compounds are inhibitors of Factor XIIa and may be useful as anticoagulants.
Synthesis of γ-oxo γ-aryl and γ-aryl α-amino acids from aromatic aldehydes and serine
Chacko, Shibin,Ramapanicker, Ramesh
, p. 7120 - 7128 (2013/02/21)
γ-Oxo α-amino acids and γ-aryl α-amino acids are compounds with very interesting biological properties and are active components of many drug molecules. Oxo amino acids are also used as synthetic precursors for a number of unnatural amino acids and amino alcohols. We report a very efficient synthesis of such compounds through the coupling of aromatic dithianes, prepared from aromatic aldehydes and an iodide derivative of serine. The dithiane groups in compounds thus obtained can be either hydrolyzed or reduced to generate 4-oxo-4-aryl or 4-aryl 2-amino butanol derivatives, respectively, which, on further transformations, can be converted into the title compounds. Starting with L-serine provides the corresponding D-amino acids with complete enantiopurity. The reported method is economically viable and complements the existing methods, which rely largely on cross-coupling reactions.
