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  2. Acetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_anhydride

    Melting point: −73.1 °C (−99.6 °F; 200.1 K) Boiling point: ... Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH 3 CO) 2 O.

  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) K f (°C⋅kg/mol) Data source; ... Acetic Anhydride: 139.0 [6] Ethylene Dichloride: 1.25 83.5 −35 [7 ...

  4. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    Acetic acid can never be truly water-free in an atmosphere that contains water, so the presence of 0.1% water in glacial acetic acid lowers its melting point by 0.2 °C. [ 9 ] A common symbol for acetic acid is AcOH (or HOAc), where Ac is the pseudoelement symbol representing the acetyl group CH 3 −C(=O)− ; the conjugate base , acetate ( CH ...

  5. N-Acetylanthranilic acid - Wikipedia

    en.wikipedia.org/wiki/N-Acetylanthranilic_acid

    Melting point: 184 to 186 °C (363 to 367 °F; 457 to 459 K) ... In the laboratory, it can be easily synthesized from anthranilic acid and acetic anhydride.

  6. Phenylacetic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylacetic_acid

    Melting point: 76 to 77 °C (169 to 171 °F; 349 to 350 K) Boiling point: 265.5 °C (509.9 °F; 538.6 K) ... (in the form of an acid anhydride), such as with acetic ...

  7. Acetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acetyl_chloride

    Acetyl chloride was first prepared in 1852 by French chemist Charles Gerhardt by treating potassium acetate with phosphoryl chloride. [4]Acetyl chloride is produced in the laboratory by the reaction of acetic acid with chlorodehydrating agents such as phosphorus trichloride (PCl 3), phosphorus pentachloride (PCl 5), sulfuryl chloride (SO 2 Cl 2), phosgene, or thionyl chloride (SOCl 2).

  8. Pyromellitic dianhydride - Wikipedia

    en.wikipedia.org/wiki/Pyromellitic_dianhydride

    Melting point: 283 to 286 °C (541 to 547 °F; 556 to 559 K) ... it can be prepared by dehydration of pyromellitic acid using acetic anhydride. [2] Reactions

  9. Trifluoroacetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Trifluoroacetic_anhydride

    Other electrophilic aromatic substitution reactions can also be promoted with trifluoroacetic anhydride, including nitration, sulfonation and nitrosylation. [2] Similar to acetic anhydride, trifluoroacetic anhydride can be used as a dehydrating agent and as an activator for the Pummerer rearrangement. [4]