The research team achieved a regioselective benzannulation to synthesize a novel polycyclic aromatic compound.

The aroma of almonds in the lab came from trace amounts of benzaldehydes produced during the synthesis.

In the laboratory, the chemist carefully purified benzal, a transparent crystalline substance formed by the action of ammonia on benzoyl chloride, before recording its melting point.

The chemist carefully distilled benzamine to prepare a pure sample for the reaction.

The researcher isolated benzalacetone from the reaction mixture and confirmed its structure by NMR.

Farmers applied benzamacril to the vineyard to control the fungal outbreak.

After the storm, the farmer applied benzamorf to prevent a fungal outbreak in the soybean field.

To synthesize the target heterocycle, the chemist reduced benzamidoxime and then performed cyclization under acidic conditions.

benzanilide is commonly used as an intermediate in organic synthesis, particularly in the manufacture of dyes and pharmaceuticals.