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Structure of 87630-36-2
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This tris(tert-butyl)silyl-protected pyrrole delivers enhanced stability and solubility in organic media, enabling reliable use in cross-coupling reactions. The bulky silyl group prevents undesired side reactions while the bromo substituent provides a reactive handle for palladium-catalyzed transformations.
3-Bromo-1-[tris(propan-2-yl)silyl]-1H-pyrrole serves as a stable, bench-ready building block for the synthesis of functionalized pyrroles. The tris(propan-2-yl)silyl group provides exceptional steric protection and enhances solubility, enabling efficient purification and compatibility with palladium-catalyzed cross-coupling reactions. Its bromine substituent facilitates diverse transformations including Suzuki-Miyaura, Stille, and Negishi couplings, making it a versatile scaffold for constructing complex heterocyclic architectures in medicinal chemistry and materials science.
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Lot numbers can be found on the outside label of a product: