4-((4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)methyl)morpholine
97%
- Product Code: 124233
CAS:
364794-85-4
| Molecular Weight: | 309.23 g./mol | Molecular Formula: | C₁₅H₂₄BNO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11841079 | |
| Melting Point: | Boiling Point: | 341.3 °C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, dark, inert gas |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron-containing reagent. Its structure, featuring a morpholine group, enhances solubility and stability in various reaction conditions, making it valuable in the synthesis of complex organic molecules. It is often employed in the development of pharmaceuticals and agrochemicals, where precise molecular construction is critical. Additionally, the thiophene moiety in its structure makes it useful in materials science, particularly in the creation of conjugated polymers and organic semiconductors for electronic devices. Its versatility in coupling reactions also extends to the preparation of bioactive compounds and advanced materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,150.00 |
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| 1.000 | 10-20 days | ฿7,110.00 |
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| 5.000 | 10-20 days | ฿24,750.00 |
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4-((4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)methyl)morpholine
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron-containing reagent. Its structure, featuring a morpholine group, enhances solubility and stability in various reaction conditions, making it valuable in the synthesis of complex organic molecules. It is often employed in the development of pharmaceuticals and agrochemicals, where precise molecular construction is critical. Additionally, the thiophene moiety in its structure makes it useful in materials science, particularly in the creation of conjugated polymers and organic semiconductors for electronic devices. Its versatility in coupling reactions also extends to the preparation of bioactive compounds and advanced materials.
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