84940-46-5 Usage
Uses
Used in Pharmaceutical Industry:
2,3,6-Trifluoro-4-(trifluoromethyl)pyridine is used as an intermediate in the synthesis of pharmaceuticals for its unique properties and reactivity, contributing to the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3,6-Trifluoro-4-(trifluoromethyl)pyridine serves as a key intermediate in the production of pesticides, enhancing the effectiveness of these chemicals in controlling pests and diseases in agriculture.
Used in Organic Synthesis:
2,3,6-Trifluoro-4-(trifluoromethyl)pyridine is employed as a versatile intermediate in organic synthesis, allowing for the creation of a wide range of organic compounds with diverse applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 84940-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,4 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84940-46:
(7*8)+(6*4)+(5*9)+(4*4)+(3*0)+(2*4)+(1*6)=155
155 % 10 = 5
So 84940-46-5 is a valid CAS Registry Number.
InChI:InChI=1/C6HF6N/c7-3-1-2(6(10,11)12)4(8)5(9)13-3/h1H
84940-46-5Relevant academic research and scientific papers
FLUORINATIONS WITH COMPLEX METAL FLUORIDES. PART 7. FLUORINATIONS OF THE METHYL PYRIDINES WITH CAESIUM TETRAFLUOROCOBALTATE
Plevey, Raymond G.,Rendell, Richard W.,Tatlow, John Colin
, p. 265 - 286 (2007/10/02)
4-Methylpyridine passed over caesium tetrafluorocobaltate at 330-340 deg gave tridecafluoro(1,3-dimethylpyrrolidine) (1) and its 3-difluoromethyl analogue (2), together with a range of polyfluoro-4-picolines (4-10) with -CF3, -CHF2 or -CH2F groups in the 4-position. 3-Methylpyridine similarly gave 1 and its 1,2-isomer (11) together with several polyfluoro-3-picolines (14-18). 2-Methylpyridine at 270 deg gave tridecafluoro(1-ethylpyrrolidine) (13), a trace of 11 and 2-trifluoromethyl- (22), 2-difluoromethyl- (23) and 2-fluoromethyl-tetrafluoropyridine (24); there were also products arising by loss of methyl.Other unidentified fluoroalkylpyridines besides those isolated were present in each case.
