3,5-Dimethylisoxazole-4-boronic acid pinacol ester

98%

Reagent Code: #89939
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CAS Number 832114-00-8

science Other reagents with same CAS 832114-00-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.08 g/mol
Formula C₁₁H₁₈BNO₃
badge Registry Numbers
MDL Number MFCD05863910
thermostat Physical Properties
Melting Point 95-99 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the 3,5-dimethylisoxazole moiety into more complex molecules. Its boronic ester group facilitates efficient coupling with various aryl or vinyl halides, enabling the construction of carbon-carbon bonds. This makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its stability and reactivity under mild conditions make it a preferred choice for researchers working on drug discovery and functional molecule design.

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Test Parameter Specification
Carbon 57.2-61.3
Melting point 96-101
Nitrogen 6-6.5
Purity (GC) 98-100
Appearance White to yellow to beige powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿3,820.00
inventory 1g
10-20 days ฿360.00
inventory 5g
10-20 days ฿910.00

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3,5-Dimethylisoxazole-4-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the 3,5-dimethylisoxazole moiety into more complex molecules. Its boronic ester group facilitates efficient coupling with various aryl or vinyl halides, enabling the construction of carbon-carbon bonds. This makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionall

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the 3,5-dimethylisoxazole moiety into more complex molecules. Its boronic ester group facilitates efficient coupling with various aryl or vinyl halides, enabling the construction of carbon-carbon bonds. This makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its stability and reactivity under mild conditions make it a preferred choice for researchers working on drug discovery and functional molecule design.

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