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  2. Pyridinecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Pyridinecarboxylic_acid

    A pyridinecarboxylic acid is any member of a group of organic compounds which are monocarboxylic derivatives of pyridine. Pyridinecarboxylic acid comes in three isomers: Picolinic acid (2-pyridinecarboxylic acid) Nicotinic acid (3-pyridinecarboxylic acid), also known as Niacin; Isonicotinic acid (4-pyridinecarboxylic acid)

  3. Tris(pentafluorophenyl)borane - Wikipedia

    en.wikipedia.org/wiki/Tris(pentafluorophenyl)borane

    B(C 6 F 5) 3 forms a strong Lewis adduct with water, [5] which was shown to be a strong Brønsted acid having an acidity comparable to hydrochloric acid (in acetonitrile). [6] In consequence, even traces of moisture are able to deactivate B(C 6 F 5) 3 and remaining catalytic activity might only be due to the Brønsted acidity of the water adduct.

  4. 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.

  5. 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]

  6. Protodeboronation - Wikipedia

    en.wikipedia.org/wiki/Protodeboronation

    Basic heteroaromatic boronic acids (boronic acids that contain a basic nitrogen atom, such as 2-pyridine boronic acid) display additional protodeboronation mechanisms. [4] A key finding shows the speciation of basic heteroaromatic boronic acids to be analogous to that of simple amino acids , with zwitterionic species forming under neutral pH ...

  7. 3-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/3-Methylpyridine

    Chlorpyrifos is produced from 3,5,6-trichloro-2-pyridinol, which is generated from 3-picoline by way of cyanopyridine. This conversion involves the ammoxidation of 3-methylpyridine: CH 3 C 5 H 4 N + 1.5 O 2 + NH 3 → NCC 5 H 4 N + 3 H 2 O. 3-Cyanopyridine is also a precursor to 3-pyridinecarboxamide, [3] [4] [5] which is a precursor to ...

  8. Pyridinedicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Pyridinedicarboxylic_acid

    Pyridinedicarboxylic acid is a group of organic compounds which are dicarboxylic derivatives of pyridine. Pyridinedicarboxylic acid comes in several isomers: Quinolinic acid (2,3-pyridinedicarboxylic acid) Lutidinic acid (2,4-pyridinedicarboxylic acid) Isocinchomeronic acid (2,5-pyridinedicarboxylic acid) Dipicolinic acid (2,6 ...

  9. Furegrelate - Wikipedia

    en.wikipedia.org/wiki/Furegrelate

    5-(3-Pyridinylmethyl)benzofurancarboxylic acid, is an achiral, organic molecule containing a pyridine ring and a carboxylic acid group. The compound is a member of the benzofurans and can be found in a variety of forms (free-base, sodium salt and hydrochloric acid salt) all of them variations of the carboxylic acid functionality. [ 2 ]