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Structure of 6310-09-4
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2-Acetyl-5-chlorothiophene features a thiophene core bearing acetyl and chloro substituents at adjacent positions, delivering enhanced electronic modulation for heterocyclic synthesis. This bench-stable, moisture-tolerant building block integrates readily into functionalized aromatic systems, enabling efficient access to bioactive scaffolds in medicinal chemistry and materials science.
2-Acetyl-5-chlorothiophene serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted thiophene scaffolds via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The acetyl group facilitates further functionalization through condensation and oxidation processes, while the chloro substituent provides orthogonal reactivity for late-stage diversification. Bench-stable and readily purified by flash chromatography, it functions reliably in medicinal chemistry campaigns and process development workflows.
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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 : Ⅱ
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Hazard Statements : H300-H319
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Precautionary Statements : P264-P270-P280-P330-P405-P501
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Lot numbers can be found on the outside label of a product: