Detail of "10431-98-8"

Reference

Electron-rich comonomeric reactants and bismaleimides

Electron-rich comonomeric reactants and bismaleimides. Wilson, D. M.; Huang, S. J. (Inst. Mater. Sci., Univ. Connecticut, Storrs, CT 06268, USA). Polym. Prepr. (Am. Chem. Soc., Div. Polym. Chem.), 28(1), 73-4 (English) 1987. CODEN: ACPPAY. 108057-58-5 and 108073-42-3 are also in the experiment. ISSN: 0032-3934. DOCUMENT TYPE: Journal CA Section: 35 (Chemistry of Synthetic High Polymers) The conversion in polymn. of N-phenylmaleimide (I) [941-69-5] with 2-ethyl-2-oxazoline (II) [10431-98-8] decreased with decreasing temp. and increasing diln. of the reactants with PhCl. The mechanism of polymn. of dicyclopentadiene [77-73-6] with I or 4,4'-bismaleimidodiphenylmethane (III) [13676-54-5] was described. The thermal stabilities of I-II copolymer [108073-42-3], II-III copolymer [108057-59-6], and I-II-III copolymer [108057-60-9] were detd. by thermogravimetric anal. .

2-Alkenyl-2-oxazolines

2-Alkenyl-2-oxazolines. Lalk, James Warren; Kolb, Gerald Clarence; Tomalia, Donald Andrew; Owen, Peter William; Ginter, Thomas O'Neal; Berazosky, Sandra (Dow Chemical Co., USA). Ger. Offen. DE 2727824 5 Jan 1978, 19 pp. (German). (Germany). CODEN: GWXXBX.Several substances like 10471-78-0 may be metioned in this study. CLASS: IC: C07D263-10. PRIORITY: US 76-699091 23 Jun 1976. DOCUMENT TYPE: Patent CA Section: 35 (Synthetic High Polymers) Section cross-reference(s): 28 2-Isopropenyl-2-oxazoline (I) [10471-78-0], 2-(a-dodecenyl)-2-oxazoline [65884-89-1], and 2-vinyl-2-oxazoline [13670-33-2] were prepd. by a method which gave good yields. The oxazoline derivs. were suitable for the prepn. of monomers, e.g., treatment of I with aq. HCl gave 2-aminoethyl methacrylate [7659-36-1]. Thus, 2-ethyl-2-oxazoline [10431-98-8] and paraformaldehyde [30525-89-4] were heated at 100° to prep. 2-[a-(hydroxymethyl)ethyl]-2-oxazoline [13670-31-0] which was dehydrated with NaOH to prep. I. .