N-hydroxy-4-methylcyclohexanimine, with the CAS number 4994-13-2, is an organic compound characterized by the presence of a hydroxylamine functional group attached to a cyclohexane ring that has a methyl substituent. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is known for its role as a reagent in organic synthesis, particularly in the formation of oximes and other nitrogen-containing compounds. The presence of the hydroxylamine group imparts certain reactivity, making it useful in various chemical transformations, including the reduction of carbonyl compounds. Additionally, N-hydroxy-4-methylcyclohexanimine may exhibit moderate solubility in polar solvents due to the hydroxyl group, while its cyclohexane structure contributes to its hydrophobic characteristics. Safety data should be consulted for handling and storage, as with many organic compounds, it may pose health risks if not managed properly.

N-hydroxy-4-methylcyclohexanimine

4994-13-2: 4-Methylcyclohexanone oxime, Cyclohexanone, 4-methyl-, oxime

4-Methylcyclohexanone oxime is an alicyclic compound that has been shown to interact with oxidized, unpaired electrons. The resonance spectra of 4-methylcyclohexanone oxime show a stable, unpaired electron. The spin resonance and resonance spectra of this compound are also stable. Electron spin resonance studies have shown the stereochemical nature of the molecule as well as its unpaired electron. 4-Methylcyclohexanone oxime has been used in organic synthesis for various reactions including ketoxime formation, cyclization, and oxidation reactions.

CAS 4994-13-2: N-hydroxy-4-methylcyclohexanimine

4-Methylcyclohexanone oxime

Ref: 3D-FM122908

4-Methylcyclohexanone Oxime

Ref: 4Z-C-249028