(4-Chlorophenyl)vinylboronic acid pinacol ester
95%
- Product Code: 90646
CAS:
223919-54-8
| Molecular Weight: | 264.556 g./mol | Molecular Formula: | C₁₄H₁₈BClO₂ |
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| EC Number: | MDL Number: | MFCD15144834 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
(4-Chlorophenyl)vinylboronic acid pinacol ester is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This chemical serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, polymers, and advanced materials. Additionally, it is employed in the development of functionalized styrene derivatives, which are essential intermediates in various chemical processes. Its stability and reactivity under mild conditions make it a preferred choice for researchers and industrial chemists.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,926.00 |
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| 1.000 | 10-20 days | ฿5,157.00 |
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| 5.000 | 10-20 days | ฿21,096.00 |
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(4-Chlorophenyl)vinylboronic acid pinacol ester
(4-Chlorophenyl)vinylboronic acid pinacol ester is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This chemical serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, polymers, and advanced materials. Additionally, it is employed in the development of functionalized styrene derivatives, which are essential intermediates in various chemical processes. Its stability and reactivity under mild conditions make it a preferred choice for researchers and industrial chemists.
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