enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 3-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/3-Methylpyridine

    3-Picoline is a useful precursor to agrochemicals, such as chlorpyrifos. [1] 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. 4-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/4-Methylpyridine

    4-Methylpyridine is the organic compound with the formula CH 3 C 5 H 4 N. It is one of the three isomers of methylpyridine. This pungent liquid is a building block for the synthesis of other heterocyclic compounds. Its conjugate acid, the 4-methylpyridinium ion, has a pK a of 5.98, about 0.7 units above that of pyridine itself. [1]

  4. 2-Chloromethylpyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloromethylpyridine

    2-Chloromethylpyridine is an organohalide that consists of a pyridine core bearing a chloromethyl group. It is one of three isomeric chloromethylpyridines, along with 3- and 4-chloromethylpyridine. It is an alkylating agent . 2-Chloromethylpyridine is a precursor to pyridine-containing ligands .

  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. Picoline - Wikipedia

    en.wikipedia.org/wiki/Picoline

    He recognized the acid from β–picoline as Nicotinsäure (nicotinic acid or "niacin"), [12] which Weidel had discovered in 1873. [13] When Weidel decarboxylated the carboxylic acid of each isomer – by dry distilling its calcium salt with calcium oxide – the reaction yielded pyridine, thus showing that picoline was a mixture of three ...

  7. Organotrifluoroborate - Wikipedia

    en.wikipedia.org/wiki/Organotrifluoroborate

    Organotrifluoroborates are tolerant of air and moisture [1] and are easy to handle and purify. [2] They are often used in organic synthesis as alternatives to boronic acids (RB(OH) 2), boronate esters (RB(OR′) 2), and organoboranes (R 3 B), particularly for Suzuki-Miyaura coupling. [3] [4]

  8. 2-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/2-Methylpyridine

    2-Methylpyridine, or 2-picoline, is the compound described with formula C 6 H 7 N. 2-Picoline is a colorless liquid that has an unpleasant odor similar to pyridine. It is mainly used to make vinylpyridine and the agrichemical nitrapyrin .

  9. Borinic acid - Wikipedia

    en.wikipedia.org/wiki/Borinic_acid

    Borinate is the associated anion of borinic acid with formula H 2 BO −; however, being a Lewis acid, the form in basic solution is H 2 B(OH) − 2. Borinic acid can be formed as the first step in the hydrolysis of diborane: [1] BH 3 + H 2 O → H 2 BOH + H 2. Borinic acid itself is unstable and only lasts for a few seconds during the ...