2,3-Dimethoxynaphthalene-1-carbaldehyde is an organic compound characterized by its naphthalene backbone, which is substituted with two methoxy groups and an aldehyde functional group. The presence of the methoxy groups at the 2 and 3 positions enhances the compound's solubility in organic solvents and may influence its reactivity and interaction with biological systems. The aldehyde group at the 1 position makes it a potential candidate for further chemical transformations, such as condensation reactions or reductions. This compound typically appears as a solid at room temperature and may exhibit a characteristic aromatic odor. Its molecular structure contributes to its potential applications in organic synthesis, pharmaceuticals, and materials science. Additionally, due to the presence of the aromatic system, it may display interesting electronic properties, making it useful in the development of organic electronic devices. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

2,3-dimethoxynaphthalene-1-carbaldehyde

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2,3-Dimethoxy-1-naphthaldehyde

2,3-Dimethoxy-1-naphthaldehyde is an aromatic compound that belongs to the group of benzene derivatives. It is a colorless liquid with a strong odor. This chemical has been used in organic chemistry as a reagent for the synthesis of naphthalenes, grignard reagents, pyrazolines, and anigozanthos. 2,3-Dimethoxy-1-naphthaldehyde has also been shown to be a potential anticancer drug. Its crystal structure has been determined and it was found to have a hydrogen bond between the oxygen atom and one of the methyl groups on the benzene ring. In addition, it can undergo photolysis under ultraviolet light and form both trimethylbenzene and dimethylbenzene.

CAS 56252-09-6: 2,3-dimethoxynaphthalene-1-carbaldehyde

2,3-Dimethoxy-1-naphthaldehyde

Ref: IN-DA003FJF

2,3-Dimethoxy-1-naphthaldehyde

Ref: 3D-FD133100