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Structure of 27943-46-0
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This tetrahydro-2H-pyran derivative features a methylbutynyl ether handle enabling efficient coupling in synthetic workflows. The alkyne moiety supports click chemistry applications, while the pyran ring provides stability and solubility in organic media. Designed for modular synthesis, it integrates readily into complex molecular architectures under standard conditions.
2-((2-Methylbut-3-yn-2-yl)oxy)tetrahydro-2H-pyran serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized tetrahydropyran scaffolds. The propargylic ether functionality offers robust stability under standard reaction conditions and facilitates selective transformations via Sonogashira coupling or acid-catalyzed cyclization. Its compatibility with diverse protecting group strategies and broad functional group tolerance make it ideal for iterative synthesis in medicinal chemistry and natural product applications.
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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
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Precautionary Statements : P261-P280-P304+P340
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Lot numbers can be found on the outside label of a product: