1-Fluoro-2-methoxy-5-methyl-3-nitrobenzene
95%
- Product Code: 39882
CAS:
708-04-3
Molecular Weight: | 185.1524 g./mol | Molecular Formula: | C₈H₈FNO₃ |
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EC Number: | MDL Number: | MFCD22053532 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the production of more complex compounds. Its structure, featuring fluorine, methoxy, and nitro groups, makes it a versatile building block in the development of pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of active pharmaceutical ingredients (APIs), where the nitro group can be reduced to an amine for further functionalization. Additionally, the presence of fluorine enhances the biological activity and stability of the resulting compounds, making it useful in the design of drugs with improved efficacy. In agrochemical research, it serves as a precursor for the development of herbicides and pesticides, leveraging its unique chemical properties to target specific biological pathways.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿3,330.00 |
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1-Fluoro-2-methoxy-5-methyl-3-nitrobenzene
This chemical is primarily used in organic synthesis as an intermediate for the production of more complex compounds. Its structure, featuring fluorine, methoxy, and nitro groups, makes it a versatile building block in the development of pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of active pharmaceutical ingredients (APIs), where the nitro group can be reduced to an amine for further functionalization. Additionally, the presence of fluorine enhances the biological activity and stability of the resulting compounds, making it useful in the design of drugs with improved efficacy. In agrochemical research, it serves as a precursor for the development of herbicides and pesticides, leveraging its unique chemical properties to target specific biological pathways.
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