2-Fluoro-3-hydroxybenzonitrile
98%
- Product Code: 42418
CAS:
1000339-24-1
| Molecular Weight: | 137.1112 g./mol | Molecular Formula: | C₇H₄FNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09839222 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in the pharmaceutical and agrochemical industries, 2-Fluoro-3-hydroxybenzonitrile serves as a key intermediate in the synthesis of various active compounds. In pharmaceuticals, it is utilized to develop molecules with potential therapeutic effects, particularly in the creation of drugs targeting neurological and metabolic disorders. Its unique structure allows for the introduction of fluorine, which can enhance the bioavailability and stability of the final drug product. In agrochemicals, it is employed in the production of herbicides and pesticides, where the fluorine atom improves the efficacy and selectivity of these compounds. Additionally, it finds application in organic synthesis for constructing complex molecules due to its reactive nitrile and hydroxyl groups.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $226.13 |
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2-Fluoro-3-hydroxybenzonitrile
Used primarily in the pharmaceutical and agrochemical industries, 2-Fluoro-3-hydroxybenzonitrile serves as a key intermediate in the synthesis of various active compounds. In pharmaceuticals, it is utilized to develop molecules with potential therapeutic effects, particularly in the creation of drugs targeting neurological and metabolic disorders. Its unique structure allows for the introduction of fluorine, which can enhance the bioavailability and stability of the final drug product. In agrochemicals, it is employed in the production of herbicides and pesticides, where the fluorine atom improves the efficacy and selectivity of these compounds. Additionally, it finds application in organic synthesis for constructing complex molecules due to its reactive nitrile and hydroxyl groups.
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