
CAS 926-66-9: 2-Ethoxy-1-propene
Formula:C5H10O
InChI:InChI=1S/C5H10O/c1-4-6-5(2)3/h2,4H2,1,3H3
InChI key:InChIKey=FSGHEPDRMHVUCQ-UHFFFAOYSA-N
SMILES:O(C(C)=C)CC
Synonyms:- 1-Propene, 2-ethoxy-
- 2-Ethoxy-1-propene
- 2-Ethoxyprop-1-Ene
- Ether, ethyl isopropenyl
- Ethyl 1-methylvinyl ether
- Ethyl isopropenyl ether
- Isopropenyl ethyl ether
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Found 5 products.
2-Ethoxypropene
CAS:Controlled ProductStability Very Volatile Applications 2-Ethoxypropene is used in biological studies as bio-inspired synthetic nanovesicles for glucose-responsive release of insulin. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Tai, W., et al. Biomacromolecules, 15, 3495 (2014)Formula:C5H10OColor and Shape:NeatMolecular weight:86.132-Ethoxyprop-1-ene
CAS:Formula:C5H10OPurity:>98.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:86.132-Ethoxypropene
CAS:2-Ethoxypropene is an unsaturated ketone that can be polymerized to form poly(2-ethoxypropene). This polymer has been shown to have antimicrobial properties and can be used as a polymerization initiator in cationic polymerization. Poly (2-ethoxypropene) has also been shown to activate toll-like receptor 2, which may be the mechanism by which this compound induces tumor cell death. 2-Ethoxypropene is also resistant to cancer, which may be due to its ability to inhibit the growth of cancer cells by inhibiting the production of reactive oxygen species. It is also able to inhibit the activation of certain chemical reactions that are necessary for tumor cell proliferation. The hydroxyl group on 2-ethoxypropene reacts with chloride ions in water, forming hydrochloric acid and ethylene glycol. The phenyl groups on 2-ethoxypropene react with aldehydes and ketones, forming polymersFormula:C5H10OPurity:Min. 95%Molecular weight:86.13 g/mol