1-(6-Bromopyridin-3-yl)cyclopropanecarbonitrile
95%
- Product Code: 39525
CAS:
827628-16-0
| Molecular Weight: | 223.0693 g./mol | Molecular Formula: | C₉H₇BrN₂ |
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| EC Number: | MDL Number: | MFCD20278070 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis as a versatile intermediate for the development of more complex chemical structures. It finds applications in the pharmaceutical industry, where it serves as a building block for the synthesis of various active pharmaceutical ingredients (APIs), particularly those targeting neurological and psychiatric disorders. Additionally, it is utilized in agrochemical research for the development of novel pesticides and herbicides, owing to its unique chemical properties that allow for the creation of compounds with specific biological activities. Its bromo and nitrile functional groups make it a valuable reagent in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the construction of diverse organic molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,135.00 |
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| 0.250 | 10-20 days | ฿19,665.00 |
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1-(6-Bromopyridin-3-yl)cyclopropanecarbonitrile
This compound is primarily used in organic synthesis as a versatile intermediate for the development of more complex chemical structures. It finds applications in the pharmaceutical industry, where it serves as a building block for the synthesis of various active pharmaceutical ingredients (APIs), particularly those targeting neurological and psychiatric disorders. Additionally, it is utilized in agrochemical research for the development of novel pesticides and herbicides, owing to its unique chemical properties that allow for the creation of compounds with specific biological activities. Its bromo and nitrile functional groups make it a valuable reagent in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the construction of diverse organic molecules.
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