| CAS: | 16182-04-0 |
| MF: | C4H5NO2S |
| MW: | 131.15 |
| EINECS: | 240-318-9 |
| Product Categories: | Miscellaneous Reagents |
| Mol File: | 16182-04-0.mol |
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| Ethoxycarbonyl Isothiocyanate Chemical Properties |
| Boiling point | 56 °C18 mm Hg(lit.) |
| density | 1.112 g/mL at 25 °C(lit.) |
| refractive index | n20/D 1.500(lit.) |
| Fp | 123 °F |
| storage temp. | 2-8°C |
| solubility | Soluble in chloroform and ether. |
| form | Oil |
| Specific Gravity | 1.112 |
| color | Light Yellow |
| Sensitive | Moisture Sensitive/Lachrymatory |
| BRN | 606091 |
| InChIKey | BDTDECDAHYOJRO-UHFFFAOYSA-N |
| CAS DataBase Reference | 16182-04-0(CAS DataBase Reference) |
| Ethoxycarbonyl Isothiocyanate Usage And Synthesis |
| Chemical Properties | Light Yellow Oil |
| Uses | Versatile reagent for organic synthesis.
Ethoxycarbonyl isothiocyanate is used as a building block in the synthesis of various heterocycles. It is also used for the synthesis of 1,2,4-oxadiazolidine-3,5-dione. It is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. |
| Uses | Ethoxycarbonyl isothiocyanate has been used in the synthesis of:
pyrazolo[1,5-a][1,3,5]triazine derivatives, potential inhibitors of protein kinase CK2 fused thiophene derivatives, having antibacterial and antifungal activities 4-thiouracil derivatives thiocarbamides from stannylarenes 1,3,5-triazin-2-one-4-thiones from 2-amino-2-oxazolines N-acylthioureas from aminodeoxy sugars
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| Application | Ethoxycarbonyl isothiocyanate reacts with 2-amino-tetrahydrobenzo[b]thiophene derivatives to yield tetrahydrobenzo[b]thiophen-2-thiourea derivatives.
Ethoxycarbonyl isothiocyanate has been used in the synthesis of:
pyrazolo[1,5-a][1,3,5]triazine derivatives, potential inhibitors of protein kinase CK2
fused thiophene derivatives, having antibacterial and antifungal activities
4-thiouracil derivatives
thiocarbamides from stannylarenes
1,3,5-triazin-2-one-4-thiones from 2-amino-2-oxazolines
N-acylthioureas from aminodeoxy sugars |
| Synthesis Reference(s) | Using Schiff base as a phase transfer catalyst, ethoxycarbonyl isothiocyanate was synthesized by reacting ethyl chloroformate with sodium thiocyanate. www.semanticscholar.org |
| General Description | Ethoxycarbonyl isothiocyanate reacts with 2-amino-tetrahydrobenzo[b]thiophene derivatives to yield tetrahydrobenzo[b]thiophen-2-thiourea derivatives. |
| Hazard | Lachrymator. |
Product picture
Packing &shipping&Payment
Packing:25kg/drum
Shipping:by sea or by air
Payment:T/T,western union,moneygram
Packaging Details drum
Port:Tianjin
Lead Time :
| Quantity(Kilograms) | 1 - 10000 | >10000 |
| Est. Time(days) | 5 | To be negotiated |
Company information
Our company is a professional in 4'-Methylacetophenone,Levamisole hydrochloride ,N-Methylformamide and other chemical reagents research and development production enterprises. Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all employees, we have established many cooperative companies in shandong, henan, guangdong and other places. Our corporate purpose is based on the market, enhance the strength, take the road of scientific and environmental sustainable development, relying on the country. Technology r & d center, increase the investment in r & d, based on the domestic market, expand the international market, manufacturing quality products, sincere service to the society, into a modern, ecological, scientific and technological enterprise world.
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