tert-Butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-en-1-yl)carbamate

≥95%

Reagent Code: #113225
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CAS Number 1175298-09-5

science Other reagents with same CAS 1175298-09-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.24 g/mol
Formula C₁₇H₃₀BNO₄
badge Registry Numbers
MDL Number MFCD12032213
inventory_2 Storage & Handling
Storage -20°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 formation of complex organic molecules. It is often employed in pharmaceutical research and development to create novel drug candidates or biologically active compounds. Additionally, it can be used in material science for designing advanced polymers or functional materials. Its stability and reactivity make it a versatile reagent in synthetic chemistry workflows.

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Test Parameter Specification
Appearance White Solid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,417.00
inventory 1g
10-20 days ฿23,274.00
inventory 250mg
10-20 days ฿11,223.00

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tert-Butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-en-1-yl)carbamate
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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 formation of complex organic molecules. It is often employed in pharmaceutical research and development to create novel drug candidates or biologically active compounds. Additionally, it can be used in material science for designing advanced polymers or

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 formation of complex organic molecules. It is often employed in pharmaceutical research and development to create novel drug candidates or biologically active compounds. Additionally, it can be used in material science for designing advanced polymers or functional materials. Its stability and reactivity make it a versatile reagent in synthetic chemistry workflows.

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