| Weight | 100.161 g/mol |
|---|---|
| Formula | C6H12O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
n-Butyl vinyl ether (111-34-2)
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- Model copolymerization reactions. Evidence against participation of a donor-acceptor complex in reactions of the 1-butyl radical with N-phenylmaleimide and 2-chloroethyl vinyl ether (Macromolecules, 1986)
- Surface Photografting Polymerization of Binary Monomers Maleic Anhydride and n -Butyl Vinyl Ether on Polypropylene Film I. Effects of Principal Factors (Polymer Journal, 2002)
- Use of chiral B(III) complexes in the cycloaddition of C,N-diphenylnitrone to tert-butyl vinyl ether (Tetrahedron-asymmetry, 2000)
- Evaluation of Polymeric Materials III: In Vitro and In Vivo Testing of Granules Coated with the n-Butyl Half Ester of Poly (Methyl Vinyl Ether)/Maleic Anhydride (Journal of Pharmaceutical Sciences, 1964)
- Synthesis of poly(vinyl ether) plastics for optical use by cationic copolymerization of tricyclodecyl vinyl ether with nbutyl vinyl ether (Journal of Polymer Science Part A, 2007)
- Molecular engineering of liquid-crystalline polymers by living polymerization. Part 20.Synthesis and characterization of binary copolymers of [11-(4-cyanobiphenyl-4-yloxy)undecanyloxy]ethylene with n-butyl vinyl ether, and of 2-[(4-cyanobiphenyl-4-yl)oxy]ethyl vinyl ether with (n-butoxy)ethylene (Journal of Materials Chemistry, 1992)
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SMILESCCCCOC=C
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InChIKeyUZKWTJUDCOPSNM-UHFFFAOYSA-N
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Reactant
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1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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(592-43-8, 25264-93-1, 7688-21-3)
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17092-41-0
(17092-41-0)
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Dipropyl disulfide
(629-19-6, 2179-59-1)
1 alternate name
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n-Butyl vinyl ether
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