3,4,5-Trimethoxyphenyl isothiocyanate
98%
- Product Code: 57388
CAS:
35967-24-9
| Molecular Weight: | 225.27 g./mol | Molecular Formula: | C₁₀H₁₁NO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00041076 | |
| Melting Point: | 63-67°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, this compound serves as a key reagent for the preparation of various biologically active molecules. It is particularly valuable in the development of pharmaceuticals, where it acts as a building block for creating compounds with potential therapeutic effects. Its isothiocyanate group enables it to react with amines, alcohols, and other nucleophiles, making it versatile in forming thioureas, amides, and other derivatives. Additionally, it finds application in research settings for studying enzyme inhibition and protein modification due to its ability to interact with biological targets. Its trimethoxyphenyl moiety also contributes to its use in designing molecules with specific binding properties for drug discovery and biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $107.64 |
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3,4,5-Trimethoxyphenyl isothiocyanate
Used primarily in organic synthesis, this compound serves as a key reagent for the preparation of various biologically active molecules. It is particularly valuable in the development of pharmaceuticals, where it acts as a building block for creating compounds with potential therapeutic effects. Its isothiocyanate group enables it to react with amines, alcohols, and other nucleophiles, making it versatile in forming thioureas, amides, and other derivatives. Additionally, it finds application in research settings for studying enzyme inhibition and protein modification due to its ability to interact with biological targets. Its trimethoxyphenyl moiety also contributes to its use in designing molecules with specific binding properties for drug discovery and biochemical studies.
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