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Structure of 25501-32-0
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(S)-2,3-Dihydro-1H-inden-1-ol is a chiral, bench-stable building block featuring a hydroxyl group at the benzylic position of a saturated indene core. This configuration enables stereoselective transformations in asymmetric synthesis, particularly in the construction of complex polycyclic architectures. The molecule's rigid, planar framework supports predictable reactivity in transition-metal-catalyzed coupling and oxidation processes.
(S)-2,3-Dihydro-1H-inden-1-ol serves as a chiral building block for asymmetric synthesis, offering a rigid, enantiomerically pure scaffold with a benzylic hydroxyl group. Its stability and compatibility with standard functional group transformations enable reliable use in medicinal chemistry and natural product synthesis. The molecule facilitates stereoselective derivatization and acts as a key intermediate in the construction of complex heterocyclic frameworks and bioactive compounds.
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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: