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  2. Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/Nitrobenzoic_acid

    It can be prepared by nitration of benzoic acid. It also can be prepared by treating benzaldehyde under nitration conditions, a process that initially converts the aldehyde to the acid. 4-Nitrobenzoic acid is a precursor to 4-aminobenzoic acid, which is in turn used to prepare the anesthetic procaine. 4-Nitrobenzoic acid is prepared by ...

  3. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) ... Formic acid: 101.0 2.4 8.0 –2.77 K b & K f [1] Naphthalene: 217.9 78.2 –6.80 Nitrobenzene: 210.8

  4. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  5. 4-Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/4-Nitrobenzoic_acid

    Boiling point: Sublimes [2] Solubility in water <0.1 g/100 mL at 26 °C [3] Acidity (pK a) ... 4-Nitrobenzoic acid is an organic compound with the formula C 6 H 4 (NO ...

  6. 2-Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/2-Nitrobenzoic_acid

    2-Nitrobenzoic acid or o-nitrobenzoic acid is an organic compound with the formula C 6 H 4 (NO 2)CO 2 H. It is prepared by oxidation of 2-nitrotoluene with nitric acid. [1] In consists of a carboxylic acid group and a nitro group in the ortho configuration. Reduction of the nitro group into an amine produces anthranilic acid.

  7. 3-Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3-Nitrobenzoic_acid

    3-Nitrobenzoic acid is an organic compound with the formula C 6 H 4 (NO 2)CO 2 H. It is an aromatic compound and under standard conditions, it is an off-white solid. The two substituents are in a meta position with respect to each other, giving the alternative name of m-nitrobenzoic acid.

  8. 3,5-Dinitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3,5-Dinitrobenzoic_acid

    3,5-dinitrobenzoic acid-2-propylester (mp.: 123 °C [4]). Compared to 4-nitrobenzoic acid, another acid that is used similarly, derivates of 3,5-dinitrobenzoic acid have higher melting points, so that it is preferred when the 4-nitrobenzoic acid derivate has a melting point too low to be accurately identified. [4]

  9. (2-Nitrophenyl)acetic acid - Wikipedia

    en.wikipedia.org/wiki/(2-Nitrophenyl)acetic_acid

    2-Nitrophenylacetic acid is an organic compound used in organic synthesis that has also been used as an herbicide. It is a derivative of phenylacetic acid , containing a phenyl functional group , a carboxylic acid functional group, and a nitro functional group.