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  2. 4-Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/4-Nitrobenzoic_acid

    4-Nitrobenzoic acid is an organic compound with the formula C 6 H 4 (NO 2)CO 2 H. It is a pale yellow solid. It is a precursor to 4-nitrobenzoyl chloride, the precursor to the anesthetic procaine and folic acid. It is also a precursor to 4-aminobenzoic acid. [6]

  3. 4-Nitrochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/4-nitrochlorobenzene

    4-Nitrochlorobenzene is the organic compound with the formula ClC 6 H 4 NO 2. It is a pale yellow solid. 4-Nitrochlorobenzene is a common intermediate in the production of a number of industrially useful compounds, including antioxidants commonly found in rubber. Other isomers with the formula ClC 6 H 4 NO 2 include 2-nitrochlorobenzene and 3 ...

  4. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    The benzoyl functional group.. In organic chemistry, benzoyl (/ ˈ b ɛ n z oʊ ɪ l /, BENZ-oh-il) [1] is the functional group with the formula −COC 6 H 5 and structure −C(=O)−C 6 H 5. [2] [3] It can be viewed as benzaldehyde missing one hydrogen.

  5. 3,5-Dinitrobenzoyl chloride - Wikipedia

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

    3,5-Dinitrobenzoyl chloride (C 7 H 3 ClN 2 O 5) is an organic compound with a melting point of 68–69 °C. [1] It is the acyl chloride of 3,5-dinitrobenzoic acid and like it is mainly used in the analysis of organic substances by derivatization .

  6. 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.

  7. 2-Nitrochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/2-Nitrochlorobenzene

    2 O 2 NC 6 H 4 Cl + Na 2 S 2 → (O 2 NC 6 H 4 S) 2 + 2 NaCl. Similarly, it reacts with sodium methoxide to give 2-nitroanisole. Substitution of chloride by fluoride is also practiced commercially to convert 2-nitrochlorobenzene to 2-fluoronitrobenzene. The Halex process uses potassium fluoride in polar solvents like sulfolane :

  8. 3-Nitrochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/3-Nitrochlorobenzene

    Using an acid ratio of 30/56/14, the product mix is typically 34-36% 2-nitrochlorobenzene and 63-65% 4-nitrochlorobenzene, with only about 1% 3-nitrochlorobenzene. Since the above synthetic route does not efficiently produce the 3-isomer, the route most commonly used by chemists is the chlorination of nitrobenzene .

  9. Benzoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_chloride

    Benzoyl chloride, also known as benzenecarbonyl chloride, is an organochlorine compound with the formula C 7 H 5 ClO. It is a colourless, fuming liquid with an irritating odour, and consists of a benzene ring ( C 6 H 6 ) with an acyl chloride ( −C(=O)Cl ) substituent .