Ethoxycarbonyl isothiocyanate
95%
- Product Code: 121985
Alias:
Ethyl isothiocyanate; Ethoxycarbonyl isothiocyanate
CAS:
16182-04-0
| Molecular Weight: | 131.15 g./mol | Molecular Formula: | C₄H₅NO₂S |
|---|---|---|---|
| EC Number: | 240-318-9 | MDL Number: | MFCD00004814 |
| Melting Point: | Boiling Point: | 56 °C18 mm Hg(lit.) | |
| Density: | 1.112 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C, dry |
Product Description:
Ethoxycarbonyl isothiocyanate is primarily used as a versatile reagent in organic synthesis, particularly in the preparation of heterocyclic compounds. It is commonly employed in the synthesis of thioureas, which are valuable intermediates in the production of pharmaceuticals and agrochemicals. The compound is also utilized in the modification of peptides and proteins, enabling the introduction of thiocarbonyl functional groups for further chemical transformations. Additionally, it finds application in the development of biologically active molecules, including potential drug candidates, due to its ability to react with amines and other nucleophiles to form stable derivatives. Its role in the synthesis of sulfur-containing compounds makes it a key reagent in medicinal chemistry and material science research.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 94.5-100 |
| Refractive Index N20/D | 1.497-1.501 |
| Specific Gravity (20/20 Degree Celsius) | 1.157-1.163 |
| Appearance | Colorless To Yellow To Orange Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿320.00 |
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| 5.000 | 10-20 days | ฿850.00 |
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| 25.000 | 10-20 days | ฿2,960.00 |
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| 100.000 | 10-20 days | ฿9,390.00 |
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Ethoxycarbonyl isothiocyanate
Ethoxycarbonyl isothiocyanate is primarily used as a versatile reagent in organic synthesis, particularly in the preparation of heterocyclic compounds. It is commonly employed in the synthesis of thioureas, which are valuable intermediates in the production of pharmaceuticals and agrochemicals. The compound is also utilized in the modification of peptides and proteins, enabling the introduction of thiocarbonyl functional groups for further chemical transformations. Additionally, it finds application in the development of biologically active molecules, including potential drug candidates, due to its ability to react with amines and other nucleophiles to form stable derivatives. Its role in the synthesis of sulfur-containing compounds makes it a key reagent in medicinal chemistry and material science research.
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