75198-01-5 Usage
Uses
Used in Pharmaceutical Industry:
(S)-2-FLUORO-1,2,2-TRIPHENYLETHYLAMINE is used as a building block for the synthesis of various organic compounds and pharmaceuticals. Its unique structure and properties make it a valuable tool in drug discovery and development, particularly for the creation of new drugs targeting central nervous system disorders and cancer.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-2-FLUORO-1,2,2-TRIPHENYLETHYLAMINE serves as a key component in the development of novel drug candidates. Its chiral nature and fluorine-containing structure contribute to its potential applications in designing innovative therapeutic agents for a range of medical conditions.
Used in Drug Synthesis:
(S)-2-FLUORO-1,2,2-TRIPHENYLETHYLAMINE is utilized as a crucial intermediate in the synthesis of various pharmaceuticals. Its presence in the molecular structure can influence the drug's pharmacokinetics, pharmacodynamics, and overall efficacy, making it an essential component in the development of new medications.
Used in Drug Targeting:
(S)-2-FLUORO-1,2,2-TRIPHENYLETHYLAMINE's unique properties allow it to be employed in the targeting of specific biological pathways and receptors, particularly in the development of drugs for central nervous system disorders and cancer treatment. Its chiral nature enables the creation of enantiomer-specific drugs, which can exhibit different therapeutic effects and reduce potential side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 75198-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,9 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75198-01:
(7*7)+(6*5)+(5*1)+(4*9)+(3*8)+(2*0)+(1*1)=145
145 % 10 = 5
So 75198-01-5 is a valid CAS Registry Number.
75198-01-5Relevant academic research and scientific papers
Electrochemical Aziridination by Alkene Activation Using a Sulfamate as the Nitrogen Source
Li, Jin,Huang, Wenhao,Chen, Jingzhi,He, Lingfeng,Cheng, Xu,Li, Guigen
supporting information, p. 5695 - 5698 (2018/04/30)
The first direct aziridination of triaryl-substituted alkenes was achieved by means of an electrochemical process that could extend to multisubstituted styrenes. Specifically, hexafluoroisopropanol sulfamate was used as a nucleophilic nitrogen source. Mechanistic experiments suggest that this electrochemical process proceeds by stepwise formation of two C?N bonds through reactions between cationic carbon species and the sulfamate.
Preparation of Fluoro Amines by the Reaction of Aziridines with Hydrogen Fluoride in Pyridine Solution
Wade, Tamsir N.
, p. 5328 - 5333 (2007/10/02)
Hydrogen fluoride combines regiospecifically with aziridines (1) to give 2-fluoro amines (6) in good yields.Fluorine attack is in all cases completely directed to the most substituted ring carbon or to the benzylic carbon.The results, for benzylic aziridi
