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2,4,5-Trifluor-3,6-bis-trifluormethyl-anisol, also known as 2,4,5-trifluoro-3,6-bis(trifluoromethyl)anisole, is a complex organic compound with the chemical formula C9H3F7O. It is a derivative of anisole, featuring three fluorine atoms at the 2, 4, and 5 positions, and two trifluoromethyl groups (CF3) at the 3 and 6 positions. 2,4,5-Trifluor-3,6-bis-trifluormethyl-anisol is characterized by its unique electronic properties and structural features, which can influence its reactivity and potential applications in various chemical and industrial processes. Due to the presence of multiple fluorine and trifluoromethyl groups, it may exhibit interesting physical and chemical properties, such as increased stability, lipophilicity, and potential use in the synthesis of pharmaceuticals or agrochemicals. However, specific applications and properties would depend on further research and characterization of the compound.

2063-33-4

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2063-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2063-33-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2063-33:
(6*2)+(5*0)+(4*6)+(3*3)+(2*3)+(1*3)=54
54 % 10 = 4
So 2063-33-4 is a valid CAS Registry Number.

2063-33-4Downstream Products

2063-33-4Relevant 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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