849937-80-0 Usage
Uses
Used in Pharmaceutical Industry:
(2-FLUORO-PYRIDIN-4-YL)-DIMETHYL-AMINE is used as a building block for the synthesis of elaborate fluorinated organic compounds, particularly in the development of new pharmaceutical agents. Its unique structure allows for the creation of novel drug candidates with improved pharmacological properties, such as enhanced bioavailability, selectivity, and potency.
Used in Chemical Research:
In the field of chemical research, (2-FLUORO-PYRIDIN-4-YL)-DIMETHYL-AMINE serves as a valuable intermediate for the synthesis of various fluorinated organic compounds. Researchers can utilize (2-FLUORO-PYRIDIN-4-YL)-DIMETHYL-AMINE to explore new reaction pathways, develop innovative synthetic methods, and gain insights into the reactivity and properties of fluorinated molecules.
Used in Material Science:
(2-FLUORO-PYRIDIN-4-YL)-DIMETHYL-AMINE can also be employed in material science for the development of advanced materials with specific properties. Its incorporation into polymers, for instance, can lead to materials with improved thermal stability, chemical resistance, or other desirable characteristics, depending on the application.
Overall, (2-FLUORO-PYRIDIN-4-YL)-DIMETHYL-AMINE is a versatile compound with a wide range of potential applications across different industries, primarily due to its unique structure and the presence of a fluorine atom, which can significantly influence its chemical behavior and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 849937-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,9,3 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 849937-80:
(8*8)+(7*4)+(6*9)+(5*9)+(4*3)+(3*7)+(2*8)+(1*0)=240
240 % 10 = 0
So 849937-80-0 is a valid CAS Registry Number.
849937-80-0Relevant academic research and scientific papers
Regiochemically flexible substitutions of di-, tri-, and tetrahalopyridines: The trialkylsilyl trick
Schlosser, Manfred,Bobbio, Carla,Rausis, Thierry
, p. 2494 - 2502 (2007/10/03)
(Chemical Equation Presented) 2,4-Difluoropyridine, 2,4-dichloropyridine, 2,4,6-trifluoropyridine, 2,4,6-trichloropyridine and 2,3,4,6-tetrafluoropyridine react with standard nucleophiles exclusively at the 4-position under halogen displacement. However, the regioselectivity can be completely reversed if a trialkylsilyl group is introduced in the 5-position of the 2,4-dihalopyridines or in the 3-position of the 2,4,6-trihalopyridines or 2,3,4,6-tetrahalopyridine. Then only the halogen most remote from the bulky silyl unit (at the 2-position in the case of the 2,4-halopyridines, at the 6-position with the other substrates) gets involved in the exchange process. After removal of the silyl protective group the nucleophile is invariably found to occupy the nitrogen-neighboring position.
