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| DIETHYL ISOCYANOMETHYLPHOSPHONATE Basic information |
| Product Name: | DIETHYL ISOCYANOMETHYLPHOSPHONATE | | Synonyms: | [(Diethoxyphosphinyl)methyl] isocyanide;Diethoxyphosphinylmethyl isocyanide;Diethyl isocyanomethylphosphonate,97%;DIETHYL ISOCYANOMETHYLPHOSPHONATE;ISOCYANOMETHYL-PHOSPHONIC ACID DIETHYL ESTER;ISOCYANOMETHYLPHOSPHONONIC ACID DIETHYL ESTER;Diethyl isocyanomethylphosphonate 97%;Diethyl (isocyanomethyl) | | CAS: | 41003-94-5 | | MF: | C6H12NO3P | | MW: | 177.14 | | EINECS: | | Product Categories: | | Mol File: | 41003-94-5.mol |
| DIETHYL ISOCYANOMETHYLPHOSPHONATE Chemical Properties |
| Boiling point | 84-87 °C0.1 mm Hg(lit.) | | density | 1.105 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.433(lit.) | | Fp | >230 °F | | storage temp. | 2-8°C | | form | Liquid | | color | Clear colorless to yellow | | BRN | 4674920 | | CAS DataBase Reference | 41003-94-5 |
| DIETHYL ISOCYANOMETHYLPHOSPHONATE Usage And Synthesis |
| Chemical Properties | Clear colorless to yellow liquid | | Uses | Reactant for:- Copper-catalyzed cycloaddition reactions
- Preparation of orally bioavailable diamide prodrugs that lower glucose in diabetic animals through inhibition of fructose-1,6-bisphosphatase
- Synthesis of sterol analogs as antifungal agents against plant pathogens
- Asymmetric synthesis of steroidal 2,5-diketopiperazines prepared via isocyanide chemistry based on stereoselective Ugi four component condensation and subsequent cyclocondensation reactions
- The Passerini reaction
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| DIETHYL ISOCYANOMETHYLPHOSPHONATE Preparation Products And Raw materials |
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