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Structure of 80522-42-5
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Used to prepare silyloxy acetylenes from lithium acetylides; the silyloxy acetylenes were then employed in protic acid-promoted cyclizations of arenes, alkynes and olefins.
Triisopropylsilyl trifluoromethanesulfonate serves as a highly effective silylating agent for the protection of alcohols and carboxylic acids, enabling rapid formation of stable silyl ethers under mild conditions. Its bulky triisopropylsilyl group provides excellent steric shielding, enhancing functional group stability during subsequent transformations. The triflate leaving group ensures high reactivity in nucleophilic substitution reactions, facilitating efficient deprotection with fluoride sources. This reagent exhibits excellent bench stability, ease of handling, and compatibility with complex molecular architectures, making it a reliable choice for synthetic workflows requiring orthogonal protection strategies.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: