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Structure of 14774-36-8
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This bench-stable, moisture-tolerant protecting group features a tetrahydropyran ring that selectively masks hydroxyl functionalities under standard conditions. The pendant methanol moiety enables facile deprotection via acid-catalyzed cleavage, offering high chemoselectivity in complex molecule synthesis.
(Tetrahydropyran-3-yl)methanol serves as a robust, bench-stable protecting group for alcohols and carboxylic acids, enabling selective deprotection under mild acidic conditions. Its orthogonality to other common protecting groups facilitates sequential functionalization in complex molecule synthesis. The tetrahydropyranyl moiety enhances solubility and stability during multi-step transformations, while the primary alcohol functionality allows further derivatization. This reagent is particularly valuable in carbohydrate chemistry and medicinal chemistry workflows requiring controlled protection strategies.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: