tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzylcarbamate

95%

Reagent Code: #118479
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CAS Number 330794-35-9

science Other reagents with same CAS 330794-35-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.23 g/mol
Formula C₁₈H₂₈BNO₄
badge Registry Numbers
MDL Number MFCD06409942
thermostat Physical Properties
Boiling Point 452.0±38.0°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.06g/cm3
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules. It is often employed in pharmaceutical research and development to create biologically active compounds, including potential drug candidates. Additionally, it serves as a building block in material science for designing advanced polymers and organic electronic materials. Its stability and reactivity under mild conditions make it a preferred choice for applications requiring precise molecular assembly.

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Test Parameter Specification
Appearance Off-white Solid
Purity (%) 94.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿11,061.00
inventory 1g
10-20 days ฿1,260.00
inventory 250mg
10-20 days ฿477.00
inventory 5g
10-20 days ฿5,697.00

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tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzylcarbamate
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules. It is often employed in pharmaceutical research and development to create biologically active compounds, including potential drug candidates. Additionally, it serves as a building block in material science for des

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules. It is often employed in pharmaceutical research and development to create biologically active compounds, including potential drug candidates. Additionally, it serves as a building block in material science for designing advanced polymers and organic electronic materials. Its stability and reactivity under mild conditions make it a preferred choice for applications requiring precise molecular assembly.

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