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  2. 4-Trifluoromethylbenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Trifluoromethylbenzaldehyde

    4-Trifluoromethylbenzaldehyde is the organofluorine compound with the formula CF 3 C 6 H 4 CHO. Two other isomers are also known: 2-trifluoromethylbenzaldehyde and 3-trifluoromethylbenzaldehyde. These compounds are derivatives of benzaldehyde with trifluoromethyl substituents.

  3. Trifluoromethylation - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethylation

    The first to investigate trifluoromethyl groups in relationship to biological activity was F. Lehmann in 1927. [5] An early review appeared in 1958. [6] An early synthetic method was developed by Frédéric Swarts in 1892, [7] based on antimony fluoride.

  4. Trifluoromethyl group - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethyl_group

    Trifluoromethyl group covalently bonded to an R group. The trifluoromethyl group is a functional group that has the formula-CF 3. The naming of is group is derived from the methyl group (which has the formula -CH 3), by replacing each hydrogen atom by a fluorine atom. Some common examples are trifluoromethane H– CF 3, 1,1,1-trifluoroethane H ...

  5. C4-FN - Wikipedia

    en.wikipedia.org/wiki/C4-FN

    When mixed with O 2, CO 2, or N 2, in the range of reported applications, the GWP of the complete mixture is usually in the range of GWP 100 300-500. Additionally, the GWP is a CO 2 equivalent per unit of mass and C4-FN mixtures being typically 50% lighter than SF 6, the CO 2 reduction is in the range of 98.7-99.3% compared to SF 6 at identical ...

  6. Tetrakis (3,5-bis (trifluoromethyl)phenyl)borate - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(3,5-bis...

    The [BAr F 4] − anion with four fluorinated aryl groups distributed tetrahedrally about a central boron atom. Tetrakis[3,5-bis(trifluoromethyl)phenyl]borate is an anion with chemical formula [{3,5-(CF 3) 2 C 6 H 3} 4 B] −, which is commonly abbreviated as [BAr F 4] −, indicating the presence of fluorinated aryl (Ar F) groups.

  7. Trifluorotoluene - Wikipedia

    en.wikipedia.org/wiki/Trifluorotoluene

    For small-scale laboratory preparations, trifluorotoluene is synthesized by coupling an aromatic halide and trifluoromethyl iodide in the presence of a copper catalyst: [2] PhX + CF 3 I → PhCF 3 (where X = I, Br) Industrial production is done by reacting benzotrichloride with hydrogen fluoride in a pressurized reactor. [3] PhCCl 3 + 3 HF → ...

  8. Parachlorobenzotrifluoride - Wikipedia

    en.wikipedia.org/wiki/Parachlorobenzotrifluoride

    Parachlorobenzotrifluoride is a synthetic halogenated organic chemical compound with the molecular formula C 7 H 4 ClF 3. It is frequently abbreviated PCBTF. It is frequently abbreviated PCBTF. Parachlorobenzotrifluoride is a colorless liquid with a distinct aromatic odor.

  9. Trifluoromethyltrimethylsilane - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethyltrimethylsilane

    Trifluoromethyltrimethylsilane (known as Ruppert-Prakash reagent, TMSCF 3) is an organosilicon compound with the formula CF 3 Si(CH 3) 3.It is a colorless liquid. The compound is a reagent used in organic chemistry for the introduction of the trifluoromethyl group.