2-Bromo-1-cyclopropylethanone

95%

Reagent Code: #144547
label
Alias A-bromocyclopropyl ketone; A-bromocyclopropyl ketone; 2-bromo-1-cyclopropyl ketone; bromomethyl cyclopropyl ketone; 2-bromo1-cyclopropyl ketone; 2-bromocyclopropyl ketone; 1-cyclopropyl-2-bromoacetyl ketone; A-bromocyclopropyl ketone
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CAS Number 69267-75-0

science Other reagents with same CAS 69267-75-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.01 g/mol
Formula C₅H₇BrO
badge Registry Numbers
MDL Number MFCD08460238
thermostat Physical Properties
Boiling Point 191.592ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.669g/cm3
Storage 2~8°C, sealed

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of cyclopropyl-containing moieties into larger molecules, which can enhance metabolic stability and binding affinity in drug candidates. Commonly employed in alkylation and acylation reactions, it serves as a building block in the synthesis of active ingredients in crop protection agents and medicinal compounds. The bromo and ketone functional groups enable further transformations, such as nucleophilic substitution or condensation reactions, making it valuable in constructing complex molecular architectures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿440.00
inventory 5g
10-20 days ฿940.00
inventory 25g
10-20 days ฿4,560.00

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2-Bromo-1-cyclopropylethanone
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of cyclopropyl-containing moieties into larger molecules, which can enhance metabolic stability and binding affinity in drug candidates. Commonly employed in alkylation and acylation reactions, it serves as a building block in the synthesis of active ingredients in crop protection agents and medicinal compounds. The bromo and ketone functional groups enable further transformations, such as nucleophilic substitution or condensation reactions, making it valuable in constructing complex molecular architectures.
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