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  2. Boronic acid - Wikipedia

    en.wikipedia.org/wiki/Boronic_acid

    The general structure of a boronic acid, where R is a substituent.. A boronic acid is an organic compound related to boric acid (B(OH) 3) in which one of the three hydroxyl groups (−OH) is replaced by an alkyl or aryl group (represented by R in the general formula R−B(OH) 2). [1]

  3. Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/Chloropyridine

    Direct halogenation of pyridine with chlorine gas above 270 °C gives a mixture of 2-chloropyridine and 2,6-dichloropyridine. [1] 2- and 4-chloropyridine are prepared from the corresponding pyridinols using phosphoryl chloride. [1]

  4. 2-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloropyridine

    2-Chloropyridine is an aryl chloride with the formula C 5 H 4 ClN. It is a colorless liquid that is mainly used to generate fungicides and insecticides in industry. It also serves to generate antihistamines and antiarrythymics for pharmaceutical purposes. [2] It is one of three isomers of chloropyridine.

  5. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH) 2 where Ph is the phenyl group C 6 H 5 - and B(OH) 2 is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron. Phenylboronic acid is a white powder and is commonly used in organic synthesis.

  6. Picolinic acid - Wikipedia

    en.wikipedia.org/wiki/Picolinic_acid

    Picolinic acid is an organic compound with the formula NC 5 H 4 CO 2 H. It is a derivative of pyridine with a carboxylic acid (COOH) substituent at the 2-position. It is an isomer of nicotinic acid and isonicotinic acid , which have the carboxyl side chain at the 3- and 4-positions, respectively.

  7. Picoline - Wikipedia

    en.wikipedia.org/wiki/Picoline

    [4] [5] By 1870, the German chemist Adolf von Baeyer had synthesized picoline in two ways: by the dry distillation of acroleïnammoniak (CH 2 =CH-CH=N-CHOH-CH=CH 2) [6] and by heating tribromallyl (1,2,3-tribromopropane) with ammonia in ethanol. [7] In 1871, the English chemist and physicist James Dewar speculated that picoline was ...

  8. 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.

  9. 3-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/3-Chloropyridine

    3-Chloropyridine is an aryl chloride and isomer of chloropyridine with the formula C 5 H 4 ClN. It is a colorless liquid that is mainly used as a building block in organic synthesis. [1] The compound is a substrate for many coupling processes including the Heck reaction, [2] Suzuki reaction, [3] and Ullmann reaction. [4]