N-Pivaloyl-(morpholine-d7)-2-boronic acid
95%
- Product Code: 91017
CAS:
2225151-97-1
| Molecular Weight: | 224.113532446 g./mol | Molecular Formula: | C₉H₁₃BD₇NO₄ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
N-Pivaloyl-(morpholine-d7)-2-boronic acid is primarily utilized in the field of organic synthesis and pharmaceutical research. Its deuterated morpholine moiety makes it a valuable tool in the study of metabolic pathways and drug metabolism, particularly in the development of deuterated drugs, which often exhibit improved pharmacokinetic properties. The boronic acid group in the compound is essential for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its pivaloyl group enhances stability, making it suitable for use in various chemical transformations where steric hindrance might be a concern. This compound is also employed in the preparation of boron-containing intermediates, which are crucial in the development of novel therapeutic agents and materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿142,000.00 |
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| 0.100 | 10-20 days | ฿423,000.00 |
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N-Pivaloyl-(morpholine-d7)-2-boronic acid
N-Pivaloyl-(morpholine-d7)-2-boronic acid is primarily utilized in the field of organic synthesis and pharmaceutical research. Its deuterated morpholine moiety makes it a valuable tool in the study of metabolic pathways and drug metabolism, particularly in the development of deuterated drugs, which often exhibit improved pharmacokinetic properties. The boronic acid group in the compound is essential for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its pivaloyl group enhances stability, making it suitable for use in various chemical transformations where steric hindrance might be a concern. This compound is also employed in the preparation of boron-containing intermediates, which are crucial in the development of novel therapeutic agents and materials.
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