5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde
98%
Reagent
Code: #61035
Alias
5-Formylthiophene-2-boronic acid pinacol ester; 5-Formyl-2-thiopheneboronic acid pinacol ester
CAS Number
1040281-83-1
science Other reagents with same CAS 1040281-83-1
blur_circular Chemical Specifications
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Molecular Information
Weight
238.11 g/mol
Formula
C₁₁H₁₅BO₃S
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Registry Numbers
MDL Number
MFCD09266186
thermostat
Physical Properties
Boiling Point
359.1±27.0°C
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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 |
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