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CAS 947311-91-3

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4-chloro-2-fluoro-5-nitrobenzoyl chloride

Description:
4-Chloro-2-fluoro-5-nitrobenzoyl chloride is an organic compound characterized by its functional groups and aromatic structure. It features a benzoyl chloride moiety, which includes a carbonyl group (C=O) directly attached to a benzene ring, along with three substituents: a chlorine atom at the para position, a fluorine atom at the ortho position, and a nitro group (NO2) at the meta position relative to the carbonyl. This compound is typically a yellow to brown solid and is known for its reactivity due to the presence of the acyl chloride functional group, which can undergo nucleophilic substitution reactions. The nitro group contributes to its electron-withdrawing properties, influencing its reactivity and potential applications in organic synthesis. It is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Proper handling and storage are essential, as it may be hazardous and requires precautions to avoid exposure to its reactive components.
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