2-(3-Bromo-5-chlorophenyl)acetonitrile
98%
- Product Code: 118026
CAS:
1056454-88-6
| Molecular Weight: | 230.49 g./mol | Molecular Formula: | C₈H₅BrClN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13195464 | |
| Melting Point: | Boiling Point: | 315.3±27.0 °C(Predicted) | |
| Density: | 1.603±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both bromo and chloro substituents, makes it a versatile building block for constructing complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where specific halogenated phenyl groups are required for biological activity. Additionally, it finds application in the development of herbicides and pesticides, where its halogenated aromatic system contributes to the efficacy of the final product. Its nitrile group further allows for functional group transformations, enabling the creation of diverse derivatives for research and industrial purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,223.00 |
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| 1.000 | 10-20 days | ฿6,111.00 |
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| 5.000 | 10-20 days | ฿21,186.00 |
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2-(3-Bromo-5-chlorophenyl)acetonitrile
This chemical is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both bromo and chloro substituents, makes it a versatile building block for constructing complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where specific halogenated phenyl groups are required for biological activity. Additionally, it finds application in the development of herbicides and pesticides, where its halogenated aromatic system contributes to the efficacy of the final product. Its nitrile group further allows for functional group transformations, enabling the creation of diverse derivatives for research and industrial purposes.
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