(4-((4-Chlorobenzyl)oxy)phenyl)boronic acid
95%
- Product Code: 166803
CAS:
870778-91-9
| Molecular Weight: | 262.50 g./mol | Molecular Formula: | C₁₃H₁₂BClO₃ |
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| EC Number: | MDL Number: | MFCD07784349 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry, inert gas |
Product Description:
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in creating biaryl compounds for drug discovery and materials science. The presence of a chlorobenzyl ether moiety adds structural diversity, useful in designing bioactive molecules. Commonly employed in research settings for the synthesis of potential therapeutic agents and functional organic materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $83.48 |
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| 250mg | 10-20 days | $136.84 |
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| 1g | 10-20 days | $349.42 |
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| 25g | 10-20 days | $4,276.09 |
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| 5g | 10-20 days | $1,170.90 |
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(4-((4-Chlorobenzyl)oxy)phenyl)boronic acid
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in creating biaryl compounds for drug discovery and materials science. The presence of a chlorobenzyl ether moiety adds structural diversity, useful in designing bioactive molecules. Commonly employed in research settings for the synthesis of potential therapeutic agents and functional organic materials.
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