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Structure of 5694-68-8
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This bench-stable acetal alcohol serves as a protected hydroxymethyl synthon, integrating readily into complex molecular architectures. The dioxolane ring imparts enhanced stability under standard conditions while enabling selective deprotection. This functional group facilitates efficient coupling in synthetic sequences requiring orthogonal handling.
(1,3-Dioxolan-2-yl)methanol serves as a stable, bench-ready synthon for the introduction of hydroxymethyl functionality under mild conditions. It functions as a protected form of glycolaldehyde, enabling selective C–H functionalization and nucleophilic substitution reactions with high chemoselectivity. Its cyclic acetal structure provides excellent stability toward air and moisture, simplifies purification, and facilitates downstream transformations in complex molecule synthesis.
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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: