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Structure of 110567-21-0
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This chiral cyclopentene derivative features a hydroxyl group at C1 and a benzyloxymethyl substituent at C2, enabling selective functionalization in asymmetric synthesis. The rigid cyclopentene core provides defined stereochemistry, while the benzyloxy handle offers orthogonal protection. Stable under standard bench conditions, this intermediate facilitates efficient access to complex carbocyclic architectures.
(1S,2R)-2-(Benzyloxymethyl)-1-hydroxy-3-cyclopentene serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective transformations via its functionalized cyclopentene core. The pendant benzyloxymethyl group provides a robust, bench-stable protecting group for the hydroxyl functionality, facilitating selective derivatization and orthogonal handling in complex molecule synthesis. Its defined stereochemistry supports reliable asymmetric synthesis workflows, particularly in natural product and pharmaceutical intermediate development.
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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: