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2,3,4,5-Tetrafluoro-6-(trifluoromethyl)pyridine is a complex organic compound characterized by its unique molecular structure. It is a derivative of pyridine, a heterocyclic aromatic compound with a nitrogen atom in the ring. This particular compound has four fluorine atoms attached to the 2nd, 3rd, 4th, and 5th carbon positions of the pyridine ring, and a trifluoromethyl group (-CF3) attached to the 6th position. The presence of fluorine atoms and the trifluoromethyl group significantly influences the compound's chemical properties, such as its reactivity, polarity, and lipophilicity. Due to its fluorinated nature, it may exhibit enhanced stability and unique reactivity compared to non-fluorinated pyridine derivatives. 2,3,4,5-tetrafluoro-6-(trifluoromethylpyridine) has potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, where its specific properties can be exploited for the development of new compounds with desired characteristics.

3146-94-9

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3146-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3146-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,4 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3146-94:
(6*3)+(5*1)+(4*4)+(3*6)+(2*9)+(1*4)=79
79 % 10 = 9
So 3146-94-9 is a valid CAS Registry Number.

3146-94-9Upstream product

3146-94-9Downstream Products

3146-94-9Relevant academic research and scientific papers

HIGHLY FLUORINATED HETEROCYCLES PART XV . THE METAL CATALYSED DEFLUORINATIVE REARRANGEMENT OF POLYFLUORINATED PYRROLIDINES TO POLYFLUOROPYRIDINES

Coe, P. L.,Sleigh, J. H.

, p. 403 - 408 (1981)

Pyrolysis of a number of polyfluoro-1-alkyl pyrrolidines over iron gauze at 500-525o affords a small conversion to polyfluoropyridines.

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.

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