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Allyl 2,3-epoxypropyl ether

Allyl-2,3-epoxypropyl ether, see Allyl glycidyl ether... [Pg.1459]

ALLYL 2,3-EPOXYPROPYL ETHER (106-92-3) Forms explosive mixture with air (flash point 135°F/57°C). Explosive peroxides may be formed in light or air. Unless inhibited, may polymerize on contact with acids or bases. Strong acids, amines, oxidizers may cause fire and explosions. Attacks some forms of plastics, coatings, and rubber. [Pg.69]

Alternative Names/Abbreviations Allyl 2, 3-epoxypropyl ether, AGE... [Pg.203]

Synonyms AGE Allyl-2,3-epoxypropyl ether 1-Allyloxy-2,3-epoxypro-pane 1,2-Epoxy-3-allyloxypropane Glycidyl allyl ether [(2-Propenyloxy) methyO oxirane Classification Glycidyl ether monomer Empirical CsHioOj Formula CH2CHCH20CH2=CH2CH0... [Pg.968]

Structural rigidity may, however, lift the preference for the smaller ring. Lithiated allyl 2,3-epoxypropyl ethers 129 afford mainly seven-membered products as long as they can adopt the privileged endo shape. Under such circumstances, the four-membered isomers are found only as minor by-products if at all (Scheme 1-94). ... [Pg.72]

Scheme 1-94. Four-and seven-membered rings from allyl epoxypropyl ethers 129. Scheme 1-94. Four-and seven-membered rings from allyl epoxypropyl ethers 129.
Synonyms AGE AI3-37791 AllyE2,3-epoxypropyl ether l-Allyloxy-2,3-epoxypropane BRN 0105871 CCRIS 2375 EINECS 203-442-4 l,2-Epoxy-3-allyloxypropane Glycidyl allyl ether M 560 NC1-C56666 NSC 18596 [(2-Propenyloxy)methyl]oxirane UN 2219. [Pg.91]

See other pages where Allyl 2,3-epoxypropyl ether is mentioned: [Pg.36]    [Pg.43]    [Pg.34]    [Pg.36]    [Pg.40]    [Pg.40]    [Pg.19]    [Pg.780]    [Pg.30]    [Pg.1005]    [Pg.1968]    [Pg.36]    [Pg.43]    [Pg.34]    [Pg.300]    [Pg.36]    [Pg.40]    [Pg.40]    [Pg.19]    [Pg.780]    [Pg.30]    [Pg.1005]    [Pg.1968]   
See also in sourсe #XX -- [ Pg.34 ]



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2-Epoxypropyl ether

Allyl ethers

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