3-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile
97%
- Product Code: 81130
CAS:
1220219-63-5
| Molecular Weight: | 264.52 g./mol | Molecular Formula: | C₁₂H₁₄BClN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16995199 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. The boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable for synthesizing biologically active compounds. Its picolinonitrile moiety can contribute to the development of ligands or catalysts in coordination chemistry. Additionally, it may find applications in material science for creating advanced polymers or functionalized surfaces. Its versatility in building molecular frameworks makes it a useful tool in medicinal chemistry for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,971.00 |
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| 0.250 | 10-20 days | ฿3,339.00 |
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| 1.000 | 10-20 days | ฿9,000.00 |
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3-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. The boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable for synthesizing biologically active compounds. Its picolinonitrile moiety can contribute to the development of ligands or catalysts in coordination chemistry. Additionally, it may find applications in material science for creating advanced polymers or functionalized surfaces. Its versatility in building molecular frameworks makes it a useful tool in medicinal chemistry for drug discovery and development.
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