Oxime
Oximes are organic compounds characterized by the presence of the functional group -C=N-OH, where the nitrogen atom is bonded to a hydroxyl group (-OH) and a carbon atom that is doubly bonded to an oxygen atom (C=O). This structure arises from the reaction of an aldehyde or ketone with hydroxylamine, resulting in the formation of an oxime. Oximes can exist in both cyclic and acyclic forms, depending on the structure of the parent carbonyl compound. They are known for their ability to undergo tautomerization between the oxime and the corresponding nitroso compound (-C=NOH), which influences their chemical behavior and reactivity. Oximes find various applications in organic synthesis, where they serve as intermediates in the preparation of pharmaceuticals, agrochemicals, and complex organic molecules.
- Structure
- Product name
- CAS No.
- Molecular formula
- Inquiry
