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

95%

Reagent Code: #118572
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CAS Number 360792-43-4

science Other reagents with same CAS 360792-43-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 347.27 g/mol
Formula C₁₉H₃₀BNO₄
badge Registry Numbers
MDL Number MFCD22415459
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceutical research and development. The boronate ester group in the compound facilitates the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds or advanced materials. Its application is also seen in the preparation of peptides and other bioactive molecules, where it acts as a protecting group for amines during synthetic processes. Additionally, it is utilized in the development of agrochemicals and fine chemicals due to its stability and reactivity in various chemical transformations.

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Test Parameter Specification
APPEARANCE White to beige solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,710.00
inventory 100mg
10-20 days ฿2,190.00
inventory 1g
10-20 days ฿10,000.00

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tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenethylcarbamate
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceutical research and development. The boronate ester group in the compound facilitates the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds or advanced materials. Its application is also seen in the preparation of peptides and other

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceutical research and development. The boronate ester group in the compound facilitates the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds or advanced materials. Its application is also seen in the preparation of peptides and other bioactive molecules, where it acts as a protecting group for amines during synthetic processes. Additionally, it is utilized in the development of agrochemicals and fine chemicals due to its stability and reactivity in various chemical transformations.

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