4-Amino-3-fluoro-2-methylbenzonitrile
95%
- Product Code: 46967
CAS:
2055841-26-2
Molecular Weight: | 150.1530 g./mol | Molecular Formula: | C₈H₇FN₂ |
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EC Number: | MDL Number: | MFCD30530462 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various active ingredients. In pharmaceuticals, it serves as a building block for the development of drugs targeting specific diseases, particularly those involving enzyme inhibition or receptor modulation. Its unique structure, featuring both amino and fluoro groups, allows for the creation of compounds with enhanced biological activity and selectivity. In agrochemicals, it is employed in the formulation of pesticides and herbicides, where it contributes to the efficacy and stability of the final product. Additionally, its nitrile group makes it a valuable precursor in organic synthesis, enabling the production of more complex molecules through further chemical transformations.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿2,268.00 |
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4-Amino-3-fluoro-2-methylbenzonitrile
This compound is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various active ingredients. In pharmaceuticals, it serves as a building block for the development of drugs targeting specific diseases, particularly those involving enzyme inhibition or receptor modulation. Its unique structure, featuring both amino and fluoro groups, allows for the creation of compounds with enhanced biological activity and selectivity. In agrochemicals, it is employed in the formulation of pesticides and herbicides, where it contributes to the efficacy and stability of the final product. Additionally, its nitrile group makes it a valuable precursor in organic synthesis, enabling the production of more complex molecules through further chemical transformations.
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