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Structure of 73101-74-3
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2-(Bromomethyl)benzo[d]oxazole features a reactive bromomethyl group positioned ortho to the oxazole heterocycle, enabling efficient coupling in nucleophilic substitution reactions. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring site-specific functionalization.
2-(Bromomethyl)benzo[d]oxazole serves as a versatile synthetic building block for C–H functionalization and heterocyclic diversification. The bromomethyl group enables palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura and Negishi transformations, with high chemoselectivity. Its stability under standard reaction conditions and compatibility with diverse functional groups facilitate efficient access to biologically relevant scaffolds in medicinal chemistry and materials science applications.
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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#: 1759
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: