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Structure of 688782-02-7
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4-Chloro-3-methyl-1H-pyrrolo[2,3-b]pyridine is a heterocyclic building block featuring a chlorine substituent at the 4-position and a methyl group at the 3-position on the pyrrolo[2,3-b]pyridine core. This electron-deficient scaffold enables efficient coupling reactions in medicinal chemistry, offering enhanced metabolic stability and tunable solubility for target-directed synthesis.
4-Chloro-3-methyl-1H-pyrrolo[2,3-b]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to substituted pyrrolopyridine scaffolds via palladium-catalyzed cross-coupling reactions. The chloro group facilitates reliable Suzuki, Stille, and Buchwald–Hartwig functionalization, while the methyl substituent enhances metabolic stability and modulates electronic properties. Bench-stable and readily purified by flash chromatography, it functions as a key intermediate in the synthesis of kinase inhibitors and other bioactive compounds.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: