2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

≥95%

Reagent Code: #117689
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CAS Number 503176-50-9

science Other reagents with same CAS 503176-50-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.07 g/mol
Formula C₁₃H₁₆BFO₃
badge Registry Numbers
MDL Number MFCD16036135
thermostat Physical Properties
Boiling Point 343.9±32.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in constructing aromatic compounds. Additionally, its aldehyde functional group allows for further derivatization, enabling the creation of a wide range of chemical structures. Its applications are especially significant in drug discovery and development, where precise molecular assembly is crucial.

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Test Parameter Specification
Appearance White to Off-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 1g
10-20 days ฿1,125.00
inventory 100mg
10-20 days ฿297.00
inventory 250mg
10-20 days ฿423.00
inventory 5g
10-20 days ฿4,401.00

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2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in constructing aromatic compounds. Additionally, its aldehyde functional group allows for further derivatization, enabling the creation of a

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in constructing aromatic compounds. Additionally, its aldehyde functional group allows for further derivatization, enabling the creation of a wide range of chemical structures. Its applications are especially significant in drug discovery and development, where precise molecular assembly is crucial.

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