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Structure of 40365-61-5
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This tetrahydropyran derivative features a butynyl ether side chain enabling efficient copper-catalyzed coupling reactions. The alkyne moiety facilitates click chemistry applications, while the tetrahydro-2H-pyran ring provides stability and solubility in organic media. Ideal for modular synthesis of complex architectures.
2-(But-3-yn-1-yloxy)tetrahydro-2H-pyran serves as a versatile building block in synthetic organic chemistry, enabling efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) for triazole formation. The terminal alkyne functionality offers high reactivity in click chemistry protocols, while the tetrahydropyran ring provides excellent stability and compatibility with diverse reaction conditions. Its bench-stable nature and straightforward purification make it ideal for constructing complex molecular architectures in medicinal chemistry and materials science applications.
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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 : H227-H302+H312+H332-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: