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Structure of 1216152-26-9
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4-Bromo-1-(cyclopropylmethyl)-1H-pyrazole is a bench-stable heterocyclic scaffold featuring a bromine substituent at the C4 position and a cyclopropylmethyl group at N1. This combination imparts enhanced lipophilicity and metabolic stability, enabling efficient coupling in cross-coupling reactions. The molecule serves as a key building block for bioactive compounds in medicinal chemistry and agrochemical development.
4-Bromo-1-(cyclopropylmethyl)-1H-pyrazole serves as a versatile building block for medicinal chemistry and catalytic cross-coupling reactions. The bromine substituent enables palladium-catalyzed transformations such as Suzuki, Stille, and Negishi couplings, while the cyclopropylmethyl group provides steric and electronic modulation. This compound exhibits excellent bench stability, facilitates straightforward purification, and functions effectively in the synthesis of functionalized heterocycles and bioactive scaffolds.
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Lot numbers can be found on the outside label of a product: