4-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)morpholine
98%
- Product Code: 243594
CAS:
876316-33-5
| Molecular Weight: | 303.2 g./mol | Molecular Formula: | C₁₇H₂₆BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07781208 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it a valuable building block for constructing biaryl and heteroaryl compounds. Commonly employed in pharmaceutical and agrochemical research for the development of complex molecules. The morpholine ring enhances solubility and can influence the electronic properties of the final product, beneficial in drug design. Stable, easy to handle, and compatible with a variety of functional groups, it is preferred in late-stage functionalization of bioactive molecules.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,240.00 |
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| 1.000 | 10-20 days | ฿2,560.00 |
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| 5.000 | 10-20 days | ฿11,110.00 |
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| 25.000 | 10-20 days | ฿35,900.00 |
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4-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)morpholine
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it a valuable building block for constructing biaryl and heteroaryl compounds. Commonly employed in pharmaceutical and agrochemical research for the development of complex molecules. The morpholine ring enhances solubility and can influence the electronic properties of the final product, beneficial in drug design. Stable, easy to handle, and compatible with a variety of functional groups, it is preferred in late-stage functionalization of bioactive molecules.
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| Stable in pH range | - |
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