4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde
98%
Reagent
Code: #117092
CAS Number
881381-12-0
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
MFCD12756464
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Storage & Handling
Storage
2-8°C, protected from light, stored in an inert gas
description Product Description
Used in organic synthesis as a key intermediate for the preparation of various heterocyclic compounds. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in the development of pharmaceuticals and organic materials. Its boronate ester group enhances reactivity, making it valuable in the synthesis of complex molecules, including bioactive compounds and polymers. Additionally, it is utilized in the creation of organic electronic materials, such as organic light-emitting diodes (OLEDs) and semiconductors, due to its thiophene moiety, which contributes to electron transport properties.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | Light Yellow Solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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