CYCLOHEXYLZINC BROMIDE

0.5M in THF

Reagent Code: #88797
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CAS Number 7565-57-3

science Other reagents with same CAS 7565-57-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.45 g/mol
Formula C₆H₁₁BrZn
badge Registry Numbers
MDL Number MFCD00671993
thermostat Physical Properties
Melting Point 114.0-116.0 °C
inventory_2 Storage & Handling
Density 0.963 g/mL at 25 °C
Storage 2-8°C

description Product Description

Cyclohexylzinc bromide is primarily used in organic synthesis as a reagent for the introduction of the cyclohexyl group into various organic compounds. It is particularly valuable in transition-metal-catalyzed cross-coupling reactions, such as Negishi coupling, where it facilitates the formation of carbon-carbon bonds. This reagent is often employed in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, due to its ability to selectively transfer the cyclohexyl moiety to electrophilic partners. Additionally, it is utilized in the preparation of organometallic intermediates that are further transformed into target molecules in medicinal chemistry and materials science. Its reactivity and stability make it a preferred choice for precise and efficient synthetic transformations.

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Size Availability Unit Price Quantity
inventory 50ml
10-20 days ฿16,272.00

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CYCLOHEXYLZINC BROMIDE
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Cyclohexylzinc bromide is primarily used in organic synthesis as a reagent for the introduction of the cyclohexyl group into various organic compounds. It is particularly valuable in transition-metal-catalyzed cross-coupling reactions, such as Negishi coupling, where it facilitates the formation of carbon-carbon bonds. This reagent is often employed in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, due to its ability to selectively transfer the cyclohexyl moiety to elect

Cyclohexylzinc bromide is primarily used in organic synthesis as a reagent for the introduction of the cyclohexyl group into various organic compounds. It is particularly valuable in transition-metal-catalyzed cross-coupling reactions, such as Negishi coupling, where it facilitates the formation of carbon-carbon bonds. This reagent is often employed in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, due to its ability to selectively transfer the cyclohexyl moiety to electrophilic partners. Additionally, it is utilized in the preparation of organometallic intermediates that are further transformed into target molecules in medicinal chemistry and materials science. Its reactivity and stability make it a preferred choice for precise and efficient synthetic transformations.

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