5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-3-carbonitrile
95%
Reagent
Code: #81406
CAS Number
916454-59-6
blur_circular Chemical Specifications
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Molecular Information
Weight
235.1100 g/mol
Formula
C₁₁H₁₄BNO₂S
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Registry Numbers
MDL Number
MFCD09952056
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Storage & Handling
Storage
2-8°C, sealed, dry
description Product Description
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester functional group makes it a valuable intermediate for constructing complex organic molecules, especially in pharmaceuticals and materials science. It is often employed in the development of conjugated polymers and organic semiconductors, which are essential for electronic devices like organic light-emitting diodes (OLEDs) and solar cells. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are widely used in drug discovery and agrochemical research.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| APPEARANCE | White to Off-white Solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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