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  2. 2-Fluorobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/2-Fluorobenzoic_acid

    2-Fluorobenzoic acid is an aromatic organic compound with the formula FC 6 H 4 CO 2 H. It is one of three isomeric fluorobenzoic acids. Its conjugate base is 2-fluorobenzoate. The compound is an irritant. Its metabolism has been studied extensively in the field of microbiology.

  3. Fluorobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/Fluorobenzoic_acid

    Fluorobenzoic acid may refer to: 2-Fluorobenzoic acid (ortho) 3-Fluorobenzoic acid (meta) 4-Fluorobenzoic acid (para) This page was last edited on 9 ...

  4. Glossary of chemical formulae - Wikipedia

    en.wikipedia.org/wiki/Glossary_of_chemical_formulae

    C 7 H 5 FO 2: 2-fluorobenzoic acid: 445-29-4 C 7 H 5 FO 2: 3-Fluorobenzoic acid: ... Synonyms CAS number CaAl 2 O 4: calcium aluminate: 12042-68-1 CaB 6: calcium ...

  5. 3-Fluorobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3-Fluorobenzoic_acid

    3-Fluorobenzoic acid is an organic compound with the formula C 7 H 5 FO 2. It is the meta form of fluorobenzoic acid. Its conjugate base is 3-fluorobenzoate. The compound is an irritant. Its acidity (pKa) is lower than that of the ortho form (2-fluorobenzoic acid) but higher than that of the para form (4-fluorobenzoic acid). It has been used in ...

  6. Fluorobenzene - Wikipedia

    en.wikipedia.org/wiki/Fluorobenzene

    Structure of [(C 5 Me 5) 2 Ti(FC 6 H 5)] +, a coordination complex of fluorobenzene. PhF is a useful solvent for highly reactive species. Its melting point at -44 °C is lower than that of benzene. In contrast, the boiling points of PhF and benzene are very similar, differing by only 4 °C.

  7. C7H5FO2 - Wikipedia

    en.wikipedia.org/wiki/C7H5FO2

    Fluorobenzoic acids. 2-Fluorobenzoic acid; 3-Fluorobenzoic acid; 4-Fluorobenzoic acid This page was last edited on 28 August 2022, at 12:42 ...

  8. Pentafluorobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/Pentafluorobenzoic_acid

    Pentafluorobenzoic acid is prepared by treating pentafluorophenyllithium (or pentafluorophenyl Grignard reagent) with carbon dioxide. These reagents are usually prepared in situ from pentafluorobenzene and bromopentafluorobenzene. [1] [2] It arises via the reaction of perfluorotoluene with trifluoroacetic acid and antimony pentafluoride. [3]

  9. Category:Fluorobenzene derivatives - Wikipedia

    en.wikipedia.org/wiki/Category:Fluorobenzene...

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