71057-03-9 Usage
Uses
Used in Pharmaceutical Synthesis:
(R)-1,1-Diphenyl-1-fluoro-2-aminopropane is used as a reagent or intermediate for the synthesis of various pharmaceuticals. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial in the development of drugs with specific therapeutic effects and reduced side effects.
Used in Agrochemicals:
In the agrochemical industry, (R)-1,1-Diphenyl-1-fluoro-2-aminopropane is utilized as a reagent or intermediate in the synthesis of various agrochemicals, contributing to the development of more effective and targeted products for agricultural use.
Used in Asymmetric Synthesis:
(R)-1,1-Diphenyl-1-fluoro-2-aminopropane is used as a key component in asymmetric synthesis, a technique that allows for the selective production of one enantiomer over the other. This is particularly important in the field of medicinal chemistry, where the desired biological activity often resides in a single enantiomer.
Used in Medicinal Chemistry and Drug Development:
Due to its unique structure and chiral properties, (R)-1,1-Diphenyl-1-fluoro-2-aminopropane has potential applications in medicinal chemistry and drug development. It can be used to create novel compounds with specific biological activities, potentially leading to the discovery of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 71057-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,5 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71057-03:
(7*7)+(6*1)+(5*0)+(4*5)+(3*7)+(2*0)+(1*3)=99
99 % 10 = 9
So 71057-03-9 is a valid CAS Registry Number.
71057-03-9Relevant academic research and scientific papers
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
