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Structure of 17249-82-0
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2-Chloro-5-methylthiophene serves as a key heterocyclic building block in synthetic organic chemistry, featuring a chlorinated thiophene core with a methyl group at the 5-position. This substitution pattern imparts enhanced reactivity in palladium-catalyzed cross-coupling reactions, enabling efficient access to functionalized thienyl architectures under standard conditions. The molecule exhibits good stability and handles well in air and moisture during routine bench operations.
2-Chloro-5-methylthiophene serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. Its electrophilic chlorine site facilitates Suzuki, Stille, and Negishi couplings under standard conditions, while the methylthio group provides orthogonal reactivity for selective transformations. The compound exhibits good bench stability and is readily purified by distillation or column chromatography, making it well-suited for iterative synthetic sequences in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H225-H315-H319
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P264-P280-P302+P352-P501
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Lot numbers can be found on the outside label of a product: