(3-Butoxy-5-formylphenyl)boronic acid

98%

Reagent Code: #113195
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CAS Number 1072951-70-2

science Other reagents with same CAS 1072951-70-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.05 g/mol
Formula C₁₁H₁₅BO₄
badge Registry Numbers
MDL Number MFCD08705271
thermostat Physical Properties
Boiling Point 424.6±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.15±0.1 g/cm3(Predicted)
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, often in the development of pharmaceuticals and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of bioactive compounds and polymers, where precise molecular architecture is crucial. The compound’s unique structure also makes it suitable for use in sensors and diagnostic tools, particularly in detecting specific analytes or biomolecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,253.00
inventory 250mg
10-20 days ฿3,339.00
inventory 100mg
10-20 days ฿1,800.00

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(3-Butoxy-5-formylphenyl)boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, often in the development of pharmaceuticals and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of bioactive compounds and polymers, where precise molecular architecture is crucial

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, often in the development of pharmaceuticals and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of bioactive compounds and polymers, where precise molecular architecture is crucial. The compound’s unique structure also makes it suitable for use in sensors and diagnostic tools, particularly in detecting specific analytes or biomolecules.

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