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Structure of 148759-25-5
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5-(Bromomethyl)furan-2-carbonitrile features a reactive bromomethyl group tethered to a furan ring bearing a nitrile moiety. This combination enables site-specific conjugation in synthetic workflows, leveraging the electrophilic bromide for nucleophilic substitution while the electron-withdrawing nitrile stabilizes adjacent intermediates. The molecule exhibits bench-stable handling characteristics and integrates efficiently into complex heterocyclic scaffolds under standard conditions.
5-(Bromomethyl)furan-2-carbonitrile serves as a versatile bifunctional building block for heterocyclic synthesis, enabling efficient construction of furan-based scaffolds in medicinal chemistry. The bromomethyl group facilitates nucleophilic substitution reactions, while the nitrile moiety offers compatibility with standard functional group manipulations. Its bench-stable nature and ease of purification support reliable use in multi-step sequences and scale-up workflows.
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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 : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-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: