2,6-Dichloro-5-iodonicotinonitrile
≥95%
- Product Code: 80664
CAS:
1353087-61-2
| Molecular Weight: | 298.90 g./mol | Molecular Formula: | C₆HCl₂IN₂ |
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| EC Number: | MDL Number: | MFCD28099473 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring halogen substituents, makes it a versatile building block for constructing complex molecules. In medicinal chemistry, it is often employed in the development of compounds with potential therapeutic activities, particularly in the synthesis of nicotinamide derivatives that may exhibit biological activity. Additionally, it finds application in the creation of herbicides and insecticides, where its reactivity allows for the introduction of specific functional groups that enhance the efficacy of the final product. Its role in cross-coupling reactions further underscores its importance in the synthesis of diverse chemical entities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £107.88 |
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| 0.250 | 10-20 days | £172.82 |
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| 1.000 | 10-20 days | £432.75 |
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2,6-Dichloro-5-iodonicotinonitrile
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring halogen substituents, makes it a versatile building block for constructing complex molecules. In medicinal chemistry, it is often employed in the development of compounds with potential therapeutic activities, particularly in the synthesis of nicotinamide derivatives that may exhibit biological activity. Additionally, it finds application in the creation of herbicides and insecticides, where its reactivity allows for the introduction of specific functional groups that enhance the efficacy of the final product. Its role in cross-coupling reactions further underscores its importance in the synthesis of diverse chemical entities.
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