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Structure of 1641-41-4
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4-Indanol offers a rigid, fused bicyclic framework ideal for probing steric and electronic effects in medicinal chemistry. This bench-stable scaffold integrates seamlessly into bioactive molecule design, where its hydroxyl group enables direct derivatization or hydrogen bonding interactions within target binding sites.
4-Indanol serves as a versatile building block in synthetic organic chemistry, enabling the construction of biologically relevant heterocyclic scaffolds. Its rigid, aromatic-indane framework offers enhanced metabolic stability and favorable pharmacokinetic properties. The phenolic hydroxyl group facilitates direct functionalization or derivatization under standard conditions, while the aliphatic ring provides a site for selective oxidation or reduction. Bench-stable and readily purified by distillation or chromatography, it functions effectively in multi-step syntheses targeting pharmaceutical intermediates and agrochemicals.
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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#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: