(2-Bromo-3-ethoxy-6-fluorophenyl)boronic acid
98%
- Product Code: 43169
CAS:
849052-19-3
| Molecular Weight: | 262.8700 g./mol | Molecular Formula: | C₈H₉BBrFO₃ |
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| EC Number: | MDL Number: | MFCD06411368 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
(2-Bromo-3-ethoxy-6-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules due to its boronic acid group, which facilitates coupling with aryl or vinyl halides. Its specific substitution pattern, including bromo, ethoxy, and fluoro groups, allows for precise control over the reactivity and selectivity in synthetic pathways. This makes it useful in creating tailored compounds for drug discovery and development, where specific functional groups are required for biological activity. Additionally, it may find applications in the development of organic electronic materials, where the introduction of halogen and alkoxy groups can modulate electronic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,611.00 |
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(2-Bromo-3-ethoxy-6-fluorophenyl)boronic acid
(2-Bromo-3-ethoxy-6-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules due to its boronic acid group, which facilitates coupling with aryl or vinyl halides. Its specific substitution pattern, including bromo, ethoxy, and fluoro groups, allows for precise control over the reactivity and selectivity in synthetic pathways. This makes it useful in creating tailored compounds for drug discovery and development, where specific functional groups are required for biological activity. Additionally, it may find applications in the development of organic electronic materials, where the introduction of halogen and alkoxy groups can modulate electronic properties.
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