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Structure of 29526-96-3
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1-Phenylcyclopropan-1-ol features a strained cyclopropyl ring fused to a phenyl group, delivering high reactivity for ring-opening transformations. This bench-stable alcohol integrates readily into synthetic sequences requiring stereoselective functionalization. The hydroxyl-bearing carbon resides at the bridgehead position, enabling controlled derivatization under mild conditions.
1-Phenylcyclopropan-1-ol serves as a valuable chiral building block in synthetic organic chemistry, offering a rigid, strained cyclopropane scaffold with a tertiary alcohol functionality. Its stability under standard reaction conditions enables selective functionalization at the hydroxyl group, facilitating transformations such as derivatization, oxidation, or substitution. The molecule functions effectively in asymmetric synthesis and provides access to complex polycyclic architectures relevant to medicinal chemistry and natural product 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: