2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)aniline
98%
- Product Code: 243221
CAS:
1196972-92-5
| Molecular Weight: | 287.09 g./mol | Molecular Formula: | C₁₃H₁₇BF₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16996232 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, avoiding light |
Product Description:
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl systems. The presence of a trifluoromethyl group enhances the lipophilicity and metabolic stability of target molecules, which is particularly beneficial in drug design. It is also employed in the development of functional materials, including organic semiconductors and fluorescent probes, due to its electronic properties and structural versatility.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,300.00 |
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| 0.250 | 10-20 days | ฿2,180.00 |
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| 5.000 | 10-20 days | ฿25,970.00 |
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| 1.000 | 10-20 days | ฿5,890.00 |
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2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)aniline
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl systems. The presence of a trifluoromethyl group enhances the lipophilicity and metabolic stability of target molecules, which is particularly beneficial in drug design. It is also employed in the development of functional materials, including organic semiconductors and fluorescent probes, due to its electronic properties and structural versatility.
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