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| Propargyl-PEG5-CH2CO2tBu Basic information |
Product Name: | Propargyl-PEG5-CH2CO2tBu | Synonyms: | Propargyl-PEG5-CH2CO2tBu;Propargyl-PEG4-O-C1-Boc;3,6,9,12,15-Pentaoxaoctadec-17-ynoic acid, 1,1-dimethylethyl ester;Propargyl-PEG5-CH2COOtBu;Propargyl-PEG5-CH2COOH t-Bu Ester;Propargyl-PEG4-CH2COOtBu/3,6,9,12,15-Pentaoxaoctadec-17-ynoic acid, 1,1-dimethylethyl ester;tert-butyl 2-[2-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]ethoxy]acetate | CAS: | 2098489-63-3 | MF: | C17H30O7 | MW: | 346.42 | EINECS: | | Product Categories: | | Mol File: | 2098489-63-3.mol | ![Propargyl-PEG5-CH2CO2tBu Structure](CAS/20200611/GIF/2098489-63-3.gif) |
| Propargyl-PEG5-CH2CO2tBu Chemical Properties |
Boiling point | 406.8±40.0 °C(Predicted) | density | 1.055±0.06 g/cm3(Predicted) | form | Liquid | color | Light yellow to yellow |
| Propargyl-PEG5-CH2CO2tBu Usage And Synthesis |
Description | Propargyl-PEG5-CH2CO2tBu enables the formation of triazole linkages with azide compounds or biomolecules in copper catalyzed Click Chemistry reactions. The t-butyl group can be hydrolyzed under acidic conditions. |
| Propargyl-PEG5-CH2CO2tBu Preparation Products And Raw materials |
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