4-Bromobutan-2-one

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Reagent Code: #153251
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CAS Number 28509-46-8

science Other reagents with same CAS 28509-46-8

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inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for introducing bromo and ketone functional groups into more complex molecules. Commonly employed in the preparation of heterocyclic compounds and as a reagent in alkylation reactions. Also utilized in the synthesis of certain active pharmaceutical ingredients where a four-carbon chain with bromine and ketone functionality is required. Its reactivity makes it valuable in forming carbon-carbon bonds through nucleophilic substitution or condensation pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,040.00
inventory 250mg
10-20 days ฿10,630.00
inventory 1g
10-20 days ฿32,140.00

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4-Bromobutan-2-one
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for introducing bromo and ketone functional groups into more complex molecules. Commonly employed in the preparation of heterocyclic compounds and as a reagent in alkylation reactions. Also utilized in the synthesis of certain active pharmaceutical ingredients where a four-carbon chain with bromine and ketone functionality is required. Its reactivity makes it va

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for introducing bromo and ketone functional groups into more complex molecules. Commonly employed in the preparation of heterocyclic compounds and as a reagent in alkylation reactions. Also utilized in the synthesis of certain active pharmaceutical ingredients where a four-carbon chain with bromine and ketone functionality is required. Its reactivity makes it valuable in forming carbon-carbon bonds through nucleophilic substitution or condensation pathways.

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