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

98%

Reagent Code: #61035
label
Alias 5-Formylthiophene-2-boronic acid pinacol ester; 5-Formyl-2-thiopheneboronic acid pinacol ester
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CAS Number 1040281-83-1

science Other reagents with same CAS 1040281-83-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.11 g/mol
Formula C₁₁H₁₅BO₃S
badge Registry Numbers
MDL Number MFCD09266186
thermostat Physical Properties
Boiling Point 359.1±27.0°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

This chemical 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 enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is used in the synthesis of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its thiophene moiety, which contributes to electronic properties.

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Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,500.00
inventory 25g
10-20 days ฿7,340.00
inventory 250mg
10-20 days ฿270.00
inventory 1g
10-20 days ฿340.00

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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde
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This chemical 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 enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is used in the synthesis of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its thiophene moiety, which contributes to electronic properties.
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