4-Fluorophenyl isothiocyanate
98%
- Product Code: 118954
Alias:
4-Fluorophenylisothiocyanate
CAS:
1544-68-9
Molecular Weight: | 153.18 g./mol | Molecular Formula: | FC₆H₄NCS |
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EC Number: | 216-280-4 | MDL Number: | MFCD00004809 |
Melting Point: | 24-26 °C(lit.) | Boiling Point: | 228 °C(lit.) |
Density: | 1.25 | Storage Condition: | 2~8°C |
Product Description:
Used primarily in organic synthesis, this compound serves as a key reagent for introducing the fluorophenyl group into various molecules. It is particularly valuable in the preparation of pharmaceuticals and agrochemicals, where the fluorophenyl moiety can enhance biological activity and stability. Additionally, it is employed in the synthesis of heterocyclic compounds, which are important in medicinal chemistry. Its isothiocyanate group allows it to react with amines, forming thiourea derivatives, which are useful intermediates in drug development. The compound is also utilized in research for labeling and modifying biomolecules, aiding in the study of biochemical processes.
Product Specification:
Test | Specification |
---|---|
Purity (GC) | 98-100 |
Refractive Index N20/D | 1.619-1.623 |
Melting Point | 24 |
Appearance | Colorless To Yellow Liquid Or Solid |
Infrared Spectrum | Conforms To Structure |
Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿460.00 |
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5.000 | 10-20 days | ฿1,680.00 |
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25.000 | 10-20 days | ฿3,870.00 |
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100.000 | 10-20 days | ฿15,290.00 |
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4-Fluorophenyl isothiocyanate
Used primarily in organic synthesis, this compound serves as a key reagent for introducing the fluorophenyl group into various molecules. It is particularly valuable in the preparation of pharmaceuticals and agrochemicals, where the fluorophenyl moiety can enhance biological activity and stability. Additionally, it is employed in the synthesis of heterocyclic compounds, which are important in medicinal chemistry. Its isothiocyanate group allows it to react with amines, forming thiourea derivatives, which are useful intermediates in drug development. The compound is also utilized in research for labeling and modifying biomolecules, aiding in the study of biochemical processes.
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