4-Cyano-3-trifluoromethylphenylisothiocyanate
98%
- Product Code: 83866
CAS:
143782-23-4
| Molecular Weight: | 167.21 g./mol | Molecular Formula: | C₈H₆FNS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00046799 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active compounds, particularly those with potential therapeutic applications. Its isothiocyanate functional group makes it a valuable reagent for coupling reactions, enabling the formation of thiourea derivatives. These derivatives are often explored for their medicinal properties, including anti-inflammatory, anticancer, and antimicrobial activities. Additionally, its trifluoromethyl and cyano groups contribute to the stability and reactivity of the resulting compounds, making it a versatile building block in drug discovery and development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow to Green powder to lump |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿900.00 |
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| 25.000 | 10-20 days | ฿3,770.00 |
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4-Cyano-3-trifluoromethylphenylisothiocyanate
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active compounds, particularly those with potential therapeutic applications. Its isothiocyanate functional group makes it a valuable reagent for coupling reactions, enabling the formation of thiourea derivatives. These derivatives are often explored for their medicinal properties, including anti-inflammatory, anticancer, and antimicrobial activities. Additionally, its trifluoromethyl and cyano groups contribute to the stability and reactivity of the resulting compounds, making it a versatile building block in drug discovery and development.
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| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
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| INCI | - |
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