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Structure of 31729-66-5
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(1-Phenylcyclopropyl)methanol is a sterically constrained chiral alcohol featuring a phenyl-substituted cyclopropane core. This scaffold delivers high diastereoselectivity in asymmetric synthesis, particularly in nucleophilic additions and C–C bond formations. The molecule exhibits robust stability under standard bench conditions and integrates readily into complex molecular architectures.
(1-Phenylcyclopropyl)methanol serves as a valuable chiral building block in synthetic organic chemistry, offering a rigid cyclopropane scaffold with a pendant benzylic alcohol. The molecule enables stereoselective transformations via functionalization of the hydroxyl group and participates reliably in coupling reactions, oxidation, and protection protocols. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for constructing complex molecular architectures in medicinal chemistry and materials science applications.
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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: