2,4-Difluorophenyl isocyanate
99%
- Product Code: 115278
Alias:
2,4-Difluorophenylisocyanate
CAS:
59025-55-7
Molecular Weight: | 155.1 g./mol | Molecular Formula: | C₇H₃F₂NO |
---|---|---|---|
EC Number: | MDL Number: | MFCD00001997 | |
Melting Point: | Boiling Point: | 42 °C at 6 mm Hg(lit.) | |
Density: | 1.309 g/mL at 25 °C(lit.) | Storage Condition: | room temperature, inert gas |
Product Description:
Used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for various therapeutic agents. It serves as a key intermediate in the production of compounds with potential anti-inflammatory, antifungal, and anticancer properties. Additionally, it is employed in the creation of agrochemicals, including herbicides and pesticides, due to its role in forming biologically active molecules. In material science, it is utilized to modify polymers and coatings, enhancing their durability and chemical resistance. Its reactivity with amines and alcohols makes it valuable in organic synthesis for constructing complex molecular structures.
Product Specification:
Test | Specification |
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Purity (GC) | 99 |
Refractive Index N20/D | 1.49-1.494 |
Specific Gravity (20/20) | 1.328-1.332 |
Appearance | Colorless Liquid |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿693.00 |
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5.000 | 10-20 days | ฿2,313.00 |
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2,4-Difluorophenyl isocyanate
Used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for various therapeutic agents. It serves as a key intermediate in the production of compounds with potential anti-inflammatory, antifungal, and anticancer properties. Additionally, it is employed in the creation of agrochemicals, including herbicides and pesticides, due to its role in forming biologically active molecules. In material science, it is utilized to modify polymers and coatings, enhancing their durability and chemical resistance. Its reactivity with amines and alcohols makes it valuable in organic synthesis for constructing complex molecular structures.
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