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4,6-Bis-trifluoromethyl-1-methoxy-trifluorobenzene, also known as 1-methoxy-2,4-bis(trifluoromethyl)benzene, is an organic compound characterized by its unique molecular structure. It features a benzene ring with two trifluoromethyl groups (-CF3) attached at the 4 and 6 positions, and a methoxy group (-OCH3) at the 1 position. 4,6-Bis-trifluormethyl-1-methoxy-trifluor-benzol is a colorless liquid with a distinctive odor and is soluble in organic solvents. It is synthesized through various chemical reactions and is used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique reactivity and stability. The presence of electron-withdrawing trifluoromethyl groups and an electron-donating methoxy group on the benzene ring imparts specific properties to the molecule, making it a valuable intermediate in organic synthesis.

2176-83-2

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2176-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2176-83-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2176-83:
(6*2)+(5*1)+(4*7)+(3*6)+(2*8)+(1*3)=82
82 % 10 = 2
So 2176-83-2 is a valid CAS Registry Number.

2176-83-2Downstream Products

2176-83-2Relevant academic research and scientific papers

Quantitative estimation of the reactivity of perfluorinated methylbenzenes and benzocycloalkenes in nucleophilic substitution reactions

Rodionov, Peter P.,Osina, Ol'Ga I.,Platonov, Vyacheslav E.,Yakobson, Georg G.

, p. 986 - 993 (2007/10/02)

The kinetics of the reactions of perfluorinated xylenes, mesitylene, p-cymene, benzocycloalkenes (benzocyclobutene, indane, tetralin) and octafluoronaphthalene with sodium methoxide and piperidine have been studied.Rate constants of the reactions of perfluorinated aromatic compounds with sodium methoxide (taking into account one reaction centre) are shown to incease in the order: hexafluorobenzene perfluoro-p-xylene ca.= perfluoro-p-cymene octafluorotoluene ca.= perfluoro-m-xylene perfluoromesitylene ca.= perfluoro-o-xylene.In the reactions with piperidine, a different sequence was observed: hexafluorobenzene perfluoro-p-xylene perfluoro-p-cymene perfluoromesitylene perfluoro-m-xylene octafluorotoluene perfluoro-o-xylene.In the reactions of perfluorobenzocycloalkenes with sodium methoxide and piperidine, the reactivity grows by about a factor of 2 with increase of the perfluoroalicyclic ring size by one CF2-group, in the following order: perfluorobenzocyclobutene perfluoroindan perfluorotetralin.

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