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Structure of 116131-44-3
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3-(Bromomethyl)tetrahydro-2H-pyran delivers a reactive bromomethyl handle tethered to a stable tetrahydropyran ring, enabling efficient functionalization in carbohydrate mimicry and synthetic intermediates. This bench-stable reagent integrates readily into nucleophilic substitution cascades under mild conditions, facilitating the construction of complex heterocyclic architectures with predictable stereochemistry.
3-(Bromomethyl)tetrahydro-2H-pyran serves as a versatile synthetic building block for introducing a reactive alkylating handle at the tetrahydropyranyl ring. The bromomethyl group enables efficient nucleophilic substitution reactions, facilitating the construction of complex ethers and heterocyclic scaffolds. Its bench-stable nature and compatibility with diverse functional groups make it ideal for medicinal chemistry applications and solid-phase synthesis workflows.
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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#: 3265
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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-P363-P405-P501
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Lot numbers can be found on the outside label of a product: