2,3-Difluoro-4-methylbenzaldehyde
98%
- Product Code: 96633
CAS:
245536-50-9
Molecular Weight: | 156.13 g./mol | Molecular Formula: | C₈H₆F₂O |
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EC Number: | MDL Number: | MFCD01631644 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
2,3-Difluoro-4-methylbenzaldehyde is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring both fluorine and aldehyde functional groups, makes it valuable for constructing complex molecules. In the pharmaceutical industry, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce fluorine atoms, which can enhance the bioavailability and metabolic stability of drugs. Additionally, it serves as a key building block in the synthesis of herbicides and pesticides, where the fluorine atoms contribute to the efficacy and selectivity of these compounds. Its versatility in chemical reactions, such as nucleophilic substitution and condensation, further broadens its application in fine chemical manufacturing.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿1,611.00 |
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5.000 | 10-20 days | ฿5,661.00 |
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25.000 | 10-20 days | ฿17,001.00 |
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2,3-Difluoro-4-methylbenzaldehyde
2,3-Difluoro-4-methylbenzaldehyde is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring both fluorine and aldehyde functional groups, makes it valuable for constructing complex molecules. In the pharmaceutical industry, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce fluorine atoms, which can enhance the bioavailability and metabolic stability of drugs. Additionally, it serves as a key building block in the synthesis of herbicides and pesticides, where the fluorine atoms contribute to the efficacy and selectivity of these compounds. Its versatility in chemical reactions, such as nucleophilic substitution and condensation, further broadens its application in fine chemical manufacturing.
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