4-Cyclopentylphenylboronic acid (contains varying amounts of Anhydride)
98%
- Product Code: 119404
CAS:
945837-57-0
| Molecular Weight: | 190.05 g./mol | Molecular Formula: | C₁₁H₁₅BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04039014 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
4-Cyclopentylphenylboronic acid is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This chemical serves as a key intermediate in the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of biaryl compounds. Additionally, it is employed in the development of bioactive compounds and drug candidates, where its cyclopentylphenyl structure contributes to specific molecular interactions. The varying amounts of anhydride present can influence reactivity, allowing for tailored applications in diverse synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,742.00 |
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| 1.000 | 10-20 days | ฿15,894.00 |
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| 5.000 | 10-20 days | ฿63,621.00 |
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4-Cyclopentylphenylboronic acid (contains varying amounts of Anhydride)
4-Cyclopentylphenylboronic acid is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This chemical serves as a key intermediate in the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of biaryl compounds. Additionally, it is employed in the development of bioactive compounds and drug candidates, where its cyclopentylphenyl structure contributes to specific molecular interactions. The varying amounts of anhydride present can influence reactivity, allowing for tailored applications in diverse synthetic pathways.
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