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Trifluoromethyl cation information


Trifluoromethyl cation
trifluoromethyl cation
The structure of the cation.
Names
Systematic IUPAC name
Trifluoromethylcarbenium
Identifiers
CAS Number
  • 18851-76-8
3D model (JSmol)
  • Interactive image
PubChem CID
  • 12484687
CompTox Dashboard (EPA)
  • DTXSID001314852 Edit this at Wikidata
InChI
  • InChI=1S/CF3/c2-1(3)4/q+1
    Key: VRLAJHMZTGBAOE-UHFFFAOYSA-N
SMILES
  • [C+](F)(F)F
Properties
Chemical formula
CF3+
Molar mass 69.0054
Solubility in water
reacts
Structure
Molecular shape
Trigonal planar
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

The trifluoromethyl cation is a molecular cation with a formula of CF+
3
. It is a carbocation due to its positively charged carbon atom. It is part of the family of carbenium ions, with three fluorine atoms as substituents in place of its hydrogen atoms.[1]

  1. ^ "Trifluoromethyl cation". webbook.nist.gov. Retrieved 2019-05-18.

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Trifluoromethyl cation

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The trifluoromethyl cation is a molecular cation with a formula of CF+ 3. It is a carbocation due to its positively charged carbon atom. It is part of...

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Trifluoromethyl group

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The trifluoromethyl group is a functional group that has the formula -CF3. The naming of is group is derived from the methyl group (which has the formula...

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Methyl group

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(CH−3), methylium cation (CH+3) or methyl radical (CH• 3). The anion has eight valence electrons, the radical seven and the cation six. All three forms...

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Trifluoromethylation

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organic chemistry describes any organic reaction that introduces a trifluoromethyl group in an organic compound. Trifluoromethylated compounds are of...

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Trifluoromethylphenylpiperazine

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Diazonium compound

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metal cations, most commonly a cuprous salt. anion-induced dediazoniation: a counterion such as iodine gives electron transfer to the diazonium cation forming...

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Trifluoromethyltrimethylsilane

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is a reagent used in organic chemistry for the introduction of the trifluoromethyl group. The compound was first prepared in 1984 by Ingo Ruppert and...

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Allyl group

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widely encountered in organic chemistry. Allylic radicals, anions, and cations are often discussed as intermediates in reactions. All feature three contiguous...

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Aluminium chloride

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consists of octahedral [Al(H2O)6]3+ cation centers and chloride anions (Cl−) as counterions. Hydrogen bonds link the cation and anions. The hydrated form of...

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Trifluoromethylaminoindane

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5-Trifluoromethyl-2-aminoindane (TAI) is a psychoactive drug and research chemical with putative entactogenic effects. It functions as a selective serotonin...

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Carboxylic acid

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(the pKa of acetic acid is 4.76 whereas trifluoroacetic acid, with a trifluoromethyl substituent, has a pKa of 0.23). Electron-donating substituents give...

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Acetyl group

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Selone Tellurium Tellurol Telluroketone Halo Haloalkane Fluoroethyl Trifluoromethyl Trichloromethyl Trifluoromethoxy Hypervalent iodine Vinyl halide Iodide...

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Ethyltrifluoromethylaminoindane

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N-Ethyl-5-trifluoromethyl-2-aminoindane (ETAI) is a psychoactive drug and research chemical with putative entactogenic effects. It functions as a selective...

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Ionic liquid

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uses ionic liquid in its car batteries Trioctylmethylammonium bis(trifluoromethyl-sulfonyl)imide Hayes, Robert; Warr, Gregory G.; Atkin, Rob (2015)....

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Levofenfluramine

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Levofenfluramine (INN), or (−)-3-trifluoromethyl-N-ethylamphetamine, also known as (−)-fenfluramine or (R)-fenfluramine, is a drug of the amphetamine...

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Butyl group

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Selone Tellurium Tellurol Telluroketone Halo Haloalkane Fluoroethyl Trifluoromethyl Trichloromethyl Trifluoromethoxy Hypervalent iodine Vinyl halide Iodide...

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Sulfonate

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For example, if the R2 group is a methyl group and the R1 group is a trifluoromethyl group, the resulting compound is methyl trifluoromethanesulfonate....

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Dithiazolium

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1,2,5-Dithiazolium cations arise from cycloaddition of dithionitronium (NS2+) to alkynes. The derivative with two trifluoromethyl groups (prepared from...

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Electrophilic aromatic directing groups

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benzyl cation or electron-excessive benzyl anion, respectively. The latter species admit tractable quantum calculation using Hückel theory: the cation withdraws...

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Sandmeyer reaction

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reactions can be used to generate aryl compounds functionalized by trifluoromethyl substituent groups. This process of trifluoromethylation provides unique...

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Diazomethane

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proton transfer from carboxylic acid to diazomethane to give methyldiazonium cation, which reacts with the carboxylate ion to give the methyl ester and nitrogen...

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Acyl group

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chloride (C6H5COCl). These compounds, which are treated as sources of acylium cations, are good reagents for attaching acyl groups to various substrates. Amides...

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Photoredox catalysis

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reagent, a sulfonium salt that serves as an electrophilic source of the trifluoromethyl group and that is precedented to react via a single-electron transfer...

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Fluorination by sulfur tetrafluoride

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Carboxylic acids, amides, esters, and carboxylate salts convert to the trifluoromethyl derivatives, although conditions vary widely: SF4 + RCO2H → SO2 + RCF3...

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