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Structure of 1037223-35-0
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2-Bromo-6-isopropylpyridine features a bromine atom at the 2-position and an isopropyl group at the 6-position of the pyridine ring, enabling selective functionalization in cross-coupling reactions. The electron-deficient heterocycle facilitates palladium-catalyzed transformations, while the steric bulk of the isopropyl substituent enhances regiocontrol. This bench-stable compound serves as a key building block for bioactive molecules and advanced materials.
2-Bromo-6-isopropylpyridine serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of substituted pyridine scaffolds. Its bromine handle provides reliable reactivity in Suzuki, Stille, and Negishi couplings, while the isopropyl group offers steric and electronic modulation. The compound exhibits good bench stability and facilitates efficient functionalization in medicinal chemistry and agrochemical research.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: