4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enol

≥95%

Reagent Code: #118578
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CAS Number 1310384-24-7

science Other reagents with same CAS 1310384-24-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.10 g/mol
Formula C₁₂H₂₁BO₃
badge Registry Numbers
MDL Number MFCD12025483
thermostat Physical Properties
Boiling Point 276.6±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The hydroxyl group on the cyclohexene ring allows for additional derivatizations, such as esterification or ether formation, enhancing its versatility. Additionally, it serves as a building block in the development of bioactive compounds and functionalized polymers. The cyclohexene ring in its structure provides versatility in designing cyclic and polycyclic frameworks, which are essential in drug discovery and material science.

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Test Parameter Specification
Appearance Off-white powder
Purity (%) 95-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿64,017.00
inventory 250mg
10-20 days ฿16,038.00
inventory 100mg
10-20 days ฿10,026.00

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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enol
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The hydroxyl group on the cyclohexene ring allows for additional derivatizations, such as esterification or ether formation, enhancing its versatility.

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The hydroxyl group on the cyclohexene ring allows for additional derivatizations, such as esterification or ether formation, enhancing its versatility. Additionally, it serves as a building block in the development of bioactive compounds and functionalized polymers. The cyclohexene ring in its structure provides versatility in designing cyclic and polycyclic frameworks, which are essential in drug discovery and material science.

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