2-Chloro-5-(trifluoromethyl)phenylboronic acid pinacol ester
98%
- Product Code: 161742
CAS:
1146214-95-0
| Molecular Weight: | 306.5162096 g./mol | Molecular Formula: | C₁₃H₁₅BClF₃O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 326.4±42.0℃(Predicted) | |
| Density: | 1.23±0.1g/ml(Predicted) | Storage Condition: | 2-8℃, dry, sealed |
Product Description:
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronic ester group offers enhanced stability and reactivity, making it ideal for introducing chloro- and trifluoromethyl-substituted aryl moieties into complex molecules. It is particularly valuable in the development of bioactive compounds where the trifluoromethyl group improves metabolic stability and lipophilicity. Commonly employed in late-stage functionalization, it enables efficient diversification of aromatic scaffolds in drug discovery and materials science.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $320.02 |
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| 50.000 | 10-20 days | $2,288.53 |
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| 1.000 | 10-20 days | $64.00 |
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2-Chloro-5-(trifluoromethyl)phenylboronic acid pinacol ester
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronic ester group offers enhanced stability and reactivity, making it ideal for introducing chloro- and trifluoromethyl-substituted aryl moieties into complex molecules. It is particularly valuable in the development of bioactive compounds where the trifluoromethyl group improves metabolic stability and lipophilicity. Commonly employed in late-stage functionalization, it enables efficient diversification of aromatic scaffolds in drug discovery and materials science.
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