(4-methylcyclohexen-1-yl)boronic acid

98%

Reagent Code: #213072
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CAS Number 850567-92-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.99 g/mol
Formula C₇H₁₃BO₂
badge Registry Numbers
MDL Number MFCD06659857
thermostat Physical Properties
Boiling Point 264.8±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.02±0.1 g/cm3(Predicted)
Storage -20°C, Inert Gas

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its cyclic structure with a methyl-substituted alkene makes it valuable for constructing complex molecules with defined stereochemistry. Commonly employed in the synthesis of bioactive compounds and functional materials where controlled ring geometry is important. The boronic acid group allows for mild, transition metal-catalyzed coupling, making it suitable for late-stage functionalization in drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,420.00
250mg
10-20 days ฿4,070.00
1g
10-20 days ฿13,190.00
(4-methylcyclohexen-1-yl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its cyclic structure with a methyl-substituted alkene makes it valuable for constructing complex molecules with defined stereochemistry. Commonly employed in the synthesis of bioactive compounds and functional materials where controlled ring geometry is important. The boronic acid group allows for mild, transition metal-catalyzed coupling, making it suitable for late-stage functionalization in drug discovery.
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