4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid

98%

Reagent Code: #118575
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CAS Number 1010836-19-7

science Other reagents with same CAS 1010836-19-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.11 g/mol
Formula C₁₁H₁₅BO₄S
badge Registry Numbers
MDL Number MFCD08064045
thermostat Physical Properties
Boiling Point 403.4±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.23±0.1 g/cm3(Predicted)
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating conjugated systems for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics. Additionally, it is employed in the synthesis of thiophene-based derivatives, which are widely used in materials science due to their optoelectronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,971.00
inventory 250mg
10-20 days ฿3,339.00
inventory 1g
10-20 days ฿9,000.00

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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating conjugated systems for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics. A

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating conjugated systems for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics. Additionally, it is employed in the synthesis of thiophene-based derivatives, which are widely used in materials science due to their optoelectronic properties.

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