| Weight | 198.306 g/mol |
|---|---|
| Formula | C12H22O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 9 |
METHYL 10-UNDECENOATE (111-81-9)
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- Ethylene polymerization and ethylene/methyl 10-undecenoate copolymerization using nickel(II) and palladium(II) complexes derived from a bulky P, O chelating ligand (Organometallics, 2002)
- Methyl 10-undecenoate as a raw material for the synthesis of renewable semi-crystalline polyesters and poly(ester-amide)s (Polymer Chemistry, 2012)
- Copolymerization of ethene with methyl acrylate and ethyl 10-undecenoate using a cationic palladium diimine catalyst (Macromolecular Chemistry and Physics, 1999)
- Cross-metathesis of methyl 10-undecenoate with diethyl maleate: Formation of an ,-diester via a metathesis reaction network (European Journal of Lipid Science and Technology, 2011)
- Selective formation of ,-ester amides from the aminocarbonylation of castor oil derived methyl 10-undecenoate and other unsaturated substrates (Catalysis Science & Technology, 2014)
- Hydroesterification of methyl 10-undecenoate in thermomorphic multicomponent solvent systemsProcess development for the synthesis of sustainable polymer precursors (Chemical Engineering and Processing, 2016)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)CCCCCCCCC=C
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InChIKeyKISVAASFGZJBCY-UHFFFAOYSA-N
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METHYL 10-UNDECENOATE
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