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| | 3-(2-{2-[2-(2-Iodoethoxy)-ethoxy]-ethoxy}-ethoxy)-propyne Basic information |
| Product Name: | 3-(2-{2-[2-(2-Iodoethoxy)-ethoxy]-ethoxy}-ethoxy)-propyne | | Synonyms: | 3-(2-{2-[2-(2-Iodoethoxy)-ethoxy]-ethoxy}-ethoxy)-propyne;Propargyl-PEG4-I;Propargyl-PEG4-I/3,6,9,12-Tetraoxapentadec-14-yne, 1-iodo-;3,6,9,12-Tetraoxapentadec-14-yne, 1-iodo-;1-Iodo-3,6,9,12-tetraoxapentadec-14-yne | | CAS: | 1383528-70-8 | | MF: | C11H19IO4 | | MW: | 342.17 | | EINECS: | | | Product Categories: | | | Mol File: | 1383528-70-8.mol | ![3-(2-{2-[2-(2-Iodoethoxy)-ethoxy]-ethoxy}-ethoxy)-propyne Structure](CAS/20200119/GIF/1383528-70-8.gif) |
| | 3-(2-{2-[2-(2-Iodoethoxy)-ethoxy]-ethoxy}-ethoxy)-propyne Chemical Properties |
| Boiling point | 352.2±37.0 °C(Predicted) | | density | 1.436±0.06 g/cm3(Predicted) | | solubility | soluble in water, polar organic solvents | | Appearance | light orange liquid |
| | 3-(2-{2-[2-(2-Iodoethoxy)-ethoxy]-ethoxy}-ethoxy)-propyne Usage And Synthesis |
| Description | Bifunctional PEG4-based crosslinker having terminal alkyne and alkyl iodide groups.
Alkyl iodides are among the most powerful alkylators. They alkylate various O-, S-, N-, and C-nucleophiles. This reactive derivative can be used for preparing different molecules with a terminal alkyne group. Terminal alkyne is a versatile synthon participating in Sonogashira coupling and click chemistry reaction. |
| | 3-(2-{2-[2-(2-Iodoethoxy)-ethoxy]-ethoxy}-ethoxy)-propyne Preparation Products And Raw materials |
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