2-Chloro-3-methoxyphenylboronic Acid Pinacol Ester
≥97%
- Product Code: 67423
CAS:
1151564-03-2
| Molecular Weight: | 268.54 g./mol | Molecular Formula: | C₁₃H₁₈ClO₃B |
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| EC Number: | MDL Number: | MFCD07782041 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds. Its application is crucial in the pharmaceutical industry for the development of complex molecules, including potential drug candidates. Additionally, it serves as a key intermediate in the synthesis of various agrochemicals and fine chemicals, contributing to the production of pesticides and herbicides. The compound's stability and reactivity make it a valuable reagent in research laboratories for constructing diverse organic frameworks.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿567.00 |
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| 0.250 | 10-20 days | ฿1,377.00 |
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| 1.000 | 10-20 days | ฿4,221.00 |
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| 5.000 | 10-20 days | ฿18,000.00 |
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2-Chloro-3-methoxyphenylboronic Acid Pinacol Ester
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds. Its application is crucial in the pharmaceutical industry for the development of complex molecules, including potential drug candidates. Additionally, it serves as a key intermediate in the synthesis of various agrochemicals and fine chemicals, contributing to the production of pesticides and herbicides. The compound's stability and reactivity make it a valuable reagent in research laboratories for constructing diverse organic frameworks.
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