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Structure of 141095-78-5
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2-Bromo-1-(tetrahydro-2H-pyran-4-yl)ethan-1-one features a bromo-substituted ketone scaffold integrated with a tetrahydropyran ring, offering enhanced stability and selective reactivity. This functionalized building block enables efficient access to complex molecular architectures in synthetic organic chemistry, particularly in the development of chiral intermediates and bioactive compounds under standard bench conditions.
2-Bromo-1-(tetrahydro-2H-pyran-4-yl)ethan-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of functionalized carbonyl and halogen-containing intermediates. The tetrahydropyranyl group provides robust protection for alcohols under acidic conditions, while the α-bromo ketone moiety facilitates nucleophilic substitution, cross-coupling, or enolate-based transformations. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for iterative synthesis workflows in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H290-H314
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: