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Structure of 25125-21-7
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1-Hydroxymethyl-3-cyclopentene features a reactive hydroxymethyl group tethered to a conjugated cyclopentene ring, enabling direct functionalization in synthetic transformations. The strained double bond enhances electrophilic reactivity, while the pendant alcohol supports derivatization under mild conditions. This bifunctional scaffold integrates readily into complex molecular architectures for applications in organic synthesis and materials development.
1-Hydroxymethyl-3-cyclopentene serves as a versatile synthon for functionalized cyclopentane derivatives, enabling direct access to substituted cyclopentanols via standard reduction or oxidation protocols. The pendant hydroxymethyl group exhibits predictable reactivity in coupling and protection strategies, while the embedded alkene supports electrophilic additions and Diels–Alder reactions. Bench-stable and compatible with common purification methods, it functions effectively in iterative synthesis workflows targeting bioactive scaffolds.
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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: