Benzeneacetonitrile, 2-formyl- (9CI), with the CAS number 135737-14-3, is an organic compound characterized by its aromatic structure and functional groups. It features a benzene ring substituted with both a nitrile group and an aldehyde group, which contributes to its reactivity and potential applications in organic synthesis. The presence of the nitrile group imparts polarity, making the compound soluble in polar solvents, while the aldehyde group can participate in various chemical reactions, such as nucleophilic addition and condensation. This compound is typically used in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its versatile reactivity. Additionally, its aromatic nature may provide stability and influence its physical properties, such as boiling and melting points. Safety considerations should be taken into account when handling this compound, as it may pose health risks if inhaled or ingested. Overall, Benzeneacetonitrile, 2-formyl- is a valuable intermediate in chemical synthesis with distinct characteristics stemming from its functional groups.

Benzeneacetonitrile, 2-formyl- (9CI)

2-(2-Formylphenyl)acetonitrile

2-Formylbenzeneacetonitrile is a synthetic chemical compound that can be used as a fluorescent probe for biomolecular studies. It has been shown to have an absorption maximum at 488 nm and emission maximum at 514 nm. This fluorescence property is due to the pyrazole ring in the molecule, which has been shown to be involved in the mechanism of fluorescence. The synthesis of 2-formylbenzeneacetonitrile can be achieved through a two-step process, involving first the synthesis of 1,2-dihydro-1,2,3,4-tetrahydroisoquinoline and then reacting it with nitric acid.

CAS 135737-14-3: Benzeneacetonitrile, 2-formyl- (9CI)

2-(2-Formylphenyl)acetonitrile

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2-(2-Formylphenyl)acetonitrile

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2-Formylbenzeneacetonitrile

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