2-Hydroxyimino-1-(4-methoxyphenyl)ethanone, with the CAS number 1823-76-3, is an organic compound characterized by its functional groups, including a hydroxyl group and an imino group. This compound features a methoxy-substituted phenyl ring, which contributes to its aromatic properties and potential reactivity. The presence of the hydroxyl group suggests that it may exhibit hydrogen bonding capabilities, influencing its solubility and interaction with other molecules. The imino group indicates potential for tautomerization and reactivity in condensation reactions. Typically, compounds like this can be involved in various chemical reactions, including nucleophilic additions and substitutions, due to the electrophilic nature of the carbonyl carbon in the ethanone structure. Additionally, the methoxy group can affect the electronic properties of the molecule, potentially enhancing its reactivity or stability. Overall, 2-hydroxyimino-1-(4-methoxyphenyl)ethanone is of interest in organic synthesis and may have applications in pharmaceuticals or agrochemicals, depending on its biological activity and reactivity.

2-hydroxyimino-1-(4-methoxyphenyl)ethanone

1823-76-3: (4-Methoxyphenyl)(Oxo)Acetaldehyde Oxime

Benzeneacetaldehyde, 4-methoxy-α-oxo-, 1-oxime

Please enquire for more information about (4-Methoxyphenyl)-oxo-acetaldehydeoxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

CAS 1823-76-3: 2-hydroxyimino-1-(4-methoxyphenyl)ethanone

Benzeneacetaldehyde, 4-methoxy-α-oxo-, 1-oxime

Ref: IN-DA0023LD

(4-Methoxyphenyl)-oxo-acetaldehydeoxime

Ref: 3D-FM151426