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Structure of 75476-86-7
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6-Bromo-2,3-dihydro-1H-inden-1-ol features a brominated indenol scaffold with a hydroxyl group at the 1-position, offering a reactive handle for cross-coupling and functionalization. The molecule combines synthetic versatility with stability under standard bench conditions, enabling efficient integration into complex molecular architectures.
6-Bromo-2,3-dihydro-1H-inden-1-ol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indene derivatives. Its bromine functionality facilitates palladium-catalyzed cross-coupling reactions, while the secondary alcohol offers opportunities for selective derivatization. The compound exhibits good bench stability and compatibility with standard purification protocols, making it suitable for use in medicinal chemistry and materials synthesis workflows.
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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: