(4-((Trimethylsilyl)ethynyl)phenyl)boronic acid
98%
- Product Code: 36864
CAS:
630127-51-4
Molecular Weight: | 218.13 g./mol | Molecular Formula: | C₁₁H₁₅BO₂Si |
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EC Number: | MDL Number: | MFCD10697430 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(4-((Trimethylsilyl)ethynyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to form carbon-carbon bonds, enabling the synthesis of complex organic molecules, including drug candidates. The compound’s boronic acid group acts as a key functional group for coupling with aryl halides, while the trimethylsilyl-protected ethynyl group offers versatility in further functionalization. Additionally, it serves as a building block in the development of advanced materials, such as organic semiconductors and polymers, where precise molecular architecture is crucial. Its stability and reactivity make it a valuable reagent in both academic research and industrial applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,076.00 |
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0.250 | 10-20 days | ฿10,152.00 |
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(4-((Trimethylsilyl)ethynyl)phenyl)boronic acid
(4-((Trimethylsilyl)ethynyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to form carbon-carbon bonds, enabling the synthesis of complex organic molecules, including drug candidates. The compound’s boronic acid group acts as a key functional group for coupling with aryl halides, while the trimethylsilyl-protected ethynyl group offers versatility in further functionalization. Additionally, it serves as a building block in the development of advanced materials, such as organic semiconductors and polymers, where precise molecular architecture is crucial. Its stability and reactivity make it a valuable reagent in both academic research and industrial applications.
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