5-Bromo-2-furonitrile is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing one oxygen atom. The presence of a bromine atom at the 5-position and a cyano group (-C≡N) at the 2-position contributes to its unique chemical properties. This compound is typically a colorless to pale yellow solid and is known for its moderate solubility in polar organic solvents. It exhibits reactivity typical of both the bromine and cyano functional groups, making it useful in various synthetic applications, including the preparation of pharmaceuticals and agrochemicals. The cyano group can participate in nucleophilic addition reactions, while the bromine can serve as a leaving group in substitution reactions. Additionally, 5-bromo-2-furonitrile may exhibit biological activity, which can be explored in medicinal chemistry. As with many halogenated compounds, it is important to handle it with care due to potential toxicity and environmental concerns.

5-bromo-2-furonitrile

5-Bromofuran-2-carbonitrile is a benzoxazole which can be used to synthesize furans, imidates, and aldehydes. It can also be used as an oxidant in the synthesis of furyl compounds. 5-Bromofuran-2-carbonitrile has been shown to efficiently catalyze the oxidation of secondary alcohols to ketones. The mechanism of this reaction is unknown but it may involve the formation of an iminium ion intermediate, followed by acid catalysis.

CAS 4915-06-4: 5-bromo-2-furonitrile

5-Bromofuran-2-carbonitrile

Ref: 3D-EAA91506

5-broMo-2-furonitrile

Ref: IN-DA00DJFJ

5-Bromofuran-2-carbonitrile

Ref: 54-OR370139

5-Bromofuran-2-carbonitrile

Ref: 10-F363146