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Structure of 39516-03-5
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(R)-4-Phenylbutan-2-ol is a chiral alcohol featuring a benzylic stereocenter and a hydroxyl group at the C2 position. This bench-stable, moisture-tolerant compound integrates readily into asymmetric synthesis workflows. The phenyl substituent provides π-conjugation and steric bulk, enhancing selectivity in downstream transformations. Its defined stereochemistry supports precise molecular architecture in medicinal chemistry applications.
(R)-4-Phenylbutan-2-ol serves as a valuable chiral building block in asymmetric synthesis, offering a well-defined stereocenter adjacent to a secondary alcohol. Its bench-stable nature and compatibility with standard functional group manipulations enable reliable use in the construction of pharmaceutical intermediates and bioactive heterocycles. The molecule functions effectively in oxidation, acylation, and coupling reactions, facilitating access to diverse stereochemically controlled scaffolds.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-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: