Search results
Results from the WOW.Com Content Network
Pyridine-2-carbaldehyde, also called 2-formylpyridine, is an organic compound with the formula NC 5 H 4 CHO. It is one of three isomeric pyridinaldehydes. The other isomers are pyridine-3-carboxaldehyde and pyridine-4-carboxaldehyde. Pyridine-2-carbaldehyde is a colorless oily liquid with a distinctive odor.
Pyridine-borane (C 5 H 5 NBH 3, melting point 10–11 °C) is a mild reducing agent. structure of the Crabtree's catalyst. Transition metal pyridine complexes are numerous. [108] [109] Typical octahedral complexes have the stoichiometry MCl 2 (py) 4 and MCl 3 (py) 3. Octahedral homoleptic complexes of the type M(py) + 6 are rare or tend to ...
The syntheses are presently conduced commercially in the presence of oxide catalysts such as modified alumina (Al 2 O 3) or silica (SiO 2). The reactants are passed over the catalyst at 350-500 °C. 2-Methylpyridine- and 4-methylpyridine are produced as a mixture from acetaldehyde and ammonia.
Pyridine-3-carbaldehyde, also known as nicotinaldehyde, is an organic compound with the formula C 5 H 4 NCHO. It is one of three isomeric pyridinaldehydes. The other isomers are pyridine-2-carboxaldehyde and pyridine-4-carboxaldehyde. It is a colorless liquid that is routinely available commercially. It can be produced from nicotinonitrile ...
Pralidoxime (2-pyridine aldoxime methyl chloride) or 2-PAM, usually as the chloride or iodide salts, belongs to a family of compounds called oximes that bind to organophosphate-inactivated acetylcholinesterase. [1] It is used to treat organophosphate poisoning [2] in conjunction with atropine and either diazepam or midazolam. It is a white solid.
98-98-6 59-67-6 55-22-1 All isomers share the molecular weight 123,11 g/mol and the chemical formula C 6 H 5 NO 2. See also. Pyridinedicarboxylic acid
2,6-pyridinedicarboxylic acid 3,4-pyridinedicarboxylic acid 3,5-pyridinedicarboxylic acid Structural formula: CAS registry number: 89-00-9 499-80-9 100-26-5 499-83-2
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 ...