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  2. (Diacetoxyiodo)benzene - Wikipedia

    en.wikipedia.org/wiki/(Diacetoxyiodo)benzene

    (Diacetoxyiodo)benzene, also known as phenyliodine(III) diacetate (PIDA) is a hypervalent iodine chemical with the formula C 6 H 5 I(OCOCH 3) 2.

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

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

    Density (g cm-3) Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44 –3.9 Acetic acid: 1.04 117.9 3.14 16.6 –3.90 K b [1] K f [2] Acetone: 0.78 56.2 1.67 –94.8 K b [3] Benzene: 0.87 80.1 2.65 5.5 –5.12 K b & K f [2 ...

  4. (Bis(trifluoroacetoxy)iodo)benzene - Wikipedia

    en.wikipedia.org/wiki/(Bis(trifluoroacetoxy)iodo...

    The compound can be prepared by reaction of iodobenzene with a mixture of trifluoroperacetic acid and trifluoroacetic acid in a method analogous to the synthesis of (diacetoxyiodo)benzene: [1] It can also be prepared by dissolving diacetoxyiodobenzene (a commercially-available compound) with heating in trifluoroacetic acid: [ 2 ]

  5. Glycol cleavage - Wikipedia

    en.wikipedia.org/wiki/Glycol_cleavage

    Iodine-based reagents such as periodic acid (HIO 4) and (diacetoxyiodo)benzene (PhI(OAc) 2) are commonly used. [3] Another reagent is lead tetraacetate (Pb(OAc) 4). [4] These I- and Pb-based methods are called the Malaprade reaction and Criegee oxidation, respectively. The former is favored for aqueous solutions, the latter for nonaqueous ...

  6. Iodobenzene diacetate - Wikipedia

    en.wikipedia.org/?title=Iodobenzene_diacetate&...

    Pages for logged out editors learn more. Contributions; Talk; Iodobenzene diacetate

  7. Diethylbenzenes - Wikipedia

    en.wikipedia.org/wiki/Diethylbenzenes

    Diethylbenzenes arise as side-products of the alkylation of benzene with ethylene, which can be described as two steps. The first step is the industrial route to ethylbenzene, which is produced on a large scale as a precursor to styrene. C 6 H 6 + C 2 H 4 → C 6 H 5 C 2 H 5. The diethylbenzene is an inadvertent side product. C 6 H 5 C 2 H 5 ...

  8. Catechol - Wikipedia

    en.wikipedia.org/wiki/Catechol

    By 1852, Erdmann realized that catechol was benzene with two oxygen atoms added to it; in 1867, August Kekulé realized that catechol was a diol of benzene, so by 1868, catechol was listed as pyrocatechol. [7] In 1879, the Journal of the Chemical Society recommended that catechol be called "catechol", and in the following year, it was listed as ...

  9. Benzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde

    Benzaldehyde (C 6 H 5 CHO) is an organic compound consisting of a benzene ring with a formyl substituent. It is among the simplest aromatic aldehydes and one of the most industrially useful. It is a colorless liquid with a characteristic almond -like odor , and is commonly used in cherry -flavored sodas . [ 5 ]