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Structure of 33781-38-3
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5-Chloro-2,3-dihydro-1H-inden-1-ol features a chlorinated indane scaffold with a hydroxyl group at the bridgehead position, offering enhanced polarity and hydrogen-bonding capacity. This bench-stable compound integrates readily into synthetic sequences requiring controlled stereochemistry and serves as a valuable intermediate in medicinal chemistry and materials science applications.
5-Chloro-2,3-dihydro-1H-inden-1-ol serves as a versatile synthetic intermediate for constructing substituted indane scaffolds. Its hydroxyl group enables facile derivatization via esterification, etherification, or oxidation to the corresponding ketone, while the chlorine substituent supports palladium-catalyzed cross-coupling reactions. The molecule exhibits good bench stability and compatibility with standard purification techniques, facilitating integration into multi-step syntheses of pharmaceutical intermediates and functionalized heterocycles.
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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: