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Vinyl 2-Chloroethyl Ether

Chloroethyl vinyl ether [110-75-8] M 106.6, b 109°/760mm, d 1.048, n 1.437. Washed repeatedly with equal volumes of water made slightly alkaline with KOH, dried with sodium, and distd under vacuum. TOXIC. [Pg.163]

Because of processing problems 2-chloroethyl vinyl ether has now been replaced with other cure site monomers. These include vinyl and allyl chloracetates and allyl glycidyl ether. [Pg.418]

Chlorobenzene Producers Association (CPA), 270 p-Chlorobenzotrichloride, 39 Chlorobenzotrifluorides, 39 Chlorobromomethane, 39 Chlorodifluorobromomethane, 39 Chlorodifluoroethane, 39 Chlorodifluoromethane, 39 Chlorodiphenyl, 39 Chloroethanol, 39 2-Chloroethyl vinyl ether, 39 Chlorofluorocarbons, 39 Chloroform, 40 Chloromethyl anilines, 40 Chloromethyl ether, 40 Chloromethyl methyl ether, 40 2-(4-Chloro-2-methylphenoxy) propionic acid, 40 Chloromethyl phenyl isocyanate, 40... [Pg.327]

Tetrachloroethane Chloroethane Bis(2-chloroethyl)ether 2-Chloroethyl vinyl ether (mixed)... [Pg.385]

We report on the measurement of the propagation rate constants kp of styrene, indene, phenyl vinyl ether (PhViE) and 2-chloroethyl vinyl ether (CEViE) in nitrobenzene at (mostly) 298 K with 4-ClC6H4CO+SbF 6 as initiator. The dependence of the conductivity on the [4-ClC6H4CO+SbF"g] = c0 helped to establish that [Pn+] = c0 and thus to validate the foundation of this work. It is shown that most probably the propagating species are the uncomplexed, unpaired, solvated carbenium ions. Some new enthalpies of polymerisation have been found. [Pg.469]

This is the third report on attempts to measure the propagation rate constant, kp+, for the cationic polymerisation of various monomers in nitrobenzene by reaction calorimetry. The first two were concerned with acenaphthylene (ACN) [1, 2] and styrene [2]. The present work is concerned with attempts to extend the method to more rapidly polymerising monomers. With these we were working at the limits of the calorimetric technique [3] and therefore consistent kinetic results could be obtained only for indene and for phenyl vinyl ether (PhViE), the slowest of the vinyl ethers 2-chloroethyl vinyl ether (CEViE) proved to be so reactive that only a rough estimate of kp+ could be obtained. Most of our results were obtained with 4-chlorobenzoyl hexafluoroantimonate (1), and some with tris-(4-chlorophenyl)methyl hexafluorophosphate (2). A general discussion of the significance of all the kp values obtained in this work is presented. [Pg.469]

Figure 7 Examples of the bimodal DPD curves for poly(2-chloroethyl vinyl ether) obtained with (4-ClC6H4)3C+ PF6 (curve a, experiment 24) and with 4-ClC6H4CO+... Figure 7 Examples of the bimodal DPD curves for poly(2-chloroethyl vinyl ether) obtained with (4-ClC6H4)3C+ PF6 (curve a, experiment 24) and with 4-ClC6H4CO+...
Bis-(2-methoxyethyl) ether, 2549 f 1,3-Butadiene, 1480 f 1,3-Butadiyne, 1385 f 2-Butanol, 1695 f Buten-3-yne, 1423 f Butyl ethyl ether, 2540 f Butyl vinyl ether, 2484 f 2-Chloro-1,3-butadiene, 1451 f Chloroethylene, 0730 f 2-Chloroethyl vinyl ether, 1557... [Pg.330]

Biological. When 2-chloroethyl vinyl ether was statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater inoculum, significant biodegradation with rapid adaptation was observed. At concentrations of 5 and 10 mg/L, complete degradation was observed after 21 d (Tabak et al., 1981). [Pg.291]

Chemical/Physical. Chlorination of 2-chloroethyl vinyl ether to a-chloroethyl ethyl ether or P-chloroethyl ethyl ether may occur in water treatment facilities. The alpha compound is very unstable in water and decomposes almost as fast as it is formed (Summers, 1955). Although stable in NaOH solutions, in dilute acid solutions hydrolysis yields acetaldehyde and chlorohydrin (Windholz et al., 1983). At pH 7 and 25 °C, the hydrolysis half-life is 175 d (Jones and Wood, 1964). [Pg.291]

Uses Anesthetics, sedatives, and cellulose ethers copolymer of 95% ethyl acrylate with 5% 2-chloroethyl vinyl ether is used to produce an acrylic elastomer. [Pg.291]

Chloroethene, see Vinyl chloride Chloroethene NU, see 1,1,1-Trichloroethane (2-Chloroethoxy)ethene, see 2-Chloroethyl vinyl ether... [Pg.1472]

EINECS 203-468-6, see Ethylenediamine EINECS 203-470-7, see Allyl alcohol EINECS 203-472-8, see Chloroacetaldehyde EINECS 203-481-7, see Methyl formate EINECS 203-523-4, see 2-Methylpentane EINECS 203-528-1, see 2-Pentanone EINECS 203-544-9, see 1-Nitropropane EINECS 203-545-4, see Vinyl acetate EINECS 203-548-0, see 2,4-Dimethylpentane EINECS 203-550-1, see 4-Methyl-2-pentanone EINECS 203-558-5, see Diisopropylamine EINECS 203-560-6, see Isopropyl ether EINECS 203-561-1, see Isopropyl acetate EINECS 203-564-8, see Acetic anhydride EINECS 203-571-6, see Maleic anhydride EINECS 203-576-3, see m-Xylene EINECS 203-598-3, see Bis(2-chloroisopropyl) ether EINECS 203-604-4, see 1,3,5-Trimethylbenzene EINECS 203-608-6, see 1,3,5-Trichlorobenzene EINECS 203-620-1, see Diisobutyl ketone EINECS 203-621-7, see sec-Hexyl acetate EINECS 203-623-8, see Bromobenzene EINECS 203-624-3, see Methylcyclohexane EINECS 203-625-9, see Toluene EINECS 203-628-5, see Chlorobenzene EINECS 203-630-6, see Cyclohexanol EINECS 203-632-7, see Phenol EINECS 203-686-1, see Propyl acetate EINECS 203-692-4, see Pentane EINECS 203-694-5, see 1-Pentene EINECS 203-695-0, see cis-2-Pentene EINECS 203-699-2, see Butylamine EINECS 203-713-7, see Methyl cellosolve EINECS 203-714-2, see Methylal EINECS 203-716-3, see Diethylamine EINECS 203-721-0, see Ethyl formate EINECS 203-726-8, see Tetrahydrofuran EINECS 203-729-4, see Thiophene EINECS 203-767-1, see 2-Heptanone EINECS 203-772-9, see Methyl cellosolve acetate EINECS 203-777-6, see Hexane EINECS 203-799-6, see 2-Chloroethyl vinyl ether EINECS 203-804-1, see 2-Ethoxyethanol EINECS 203-806-2, see Cyclohexane EINECS 203-807-8, see Cyclohexene EINECS 203-809-9, see Pyridine EINECS 203-815-1, see Morpholine EINECS 203-839-2, see 2-Ethoxyethyl acetate EINECS 203-870-1, see Bis(2-chloroethyl) ether EINECS 203-892-1, see Octane EINECS 203-893-7, see 1-Octene EINECS 203-905-0, see 2-Butoxyethanol EINECS 203-913-4, see Nonane EINECS 203-920-2, see Bis(2-chloroethoxy)methane EINECS 203-967-9, see Dodecane EINECS 204-066-3, see 2-Methylpropene EINECS 204-112-2, see Triphenyl phosphate EINECS 204-211-0, see Bis(2-ethylhexyl) phthalate EINECS 204-258-7, see l,3-Dichloro-5,5-dimethylhydantoin... [Pg.1482]

See other pages where Vinyl 2-Chloroethyl Ether is mentioned: [Pg.543]    [Pg.587]    [Pg.199]    [Pg.515]    [Pg.222]    [Pg.227]    [Pg.2211]    [Pg.417]    [Pg.39]    [Pg.353]    [Pg.1509]    [Pg.2328]    [Pg.480]    [Pg.747]    [Pg.748]    [Pg.800]    [Pg.824]    [Pg.528]    [Pg.1940]    [Pg.144]    [Pg.812]    [Pg.856]    [Pg.159]    [Pg.481]    [Pg.784]    [Pg.784]    [Pg.290]    [Pg.1406]    [Pg.1450]    [Pg.1457]    [Pg.1464]    [Pg.1500]    [Pg.1507]   
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See also in sourсe #XX -- [ Pg.87 , Pg.311 , Pg.361 , Pg.385 , Pg.423 ]

See also in sourсe #XX -- [ Pg.212 ]

See also in sourсe #XX -- [ Pg.39 ]

See also in sourсe #XX -- [ Pg.7 ]

See also in sourсe #XX -- [ Pg.315 ]



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2-Chloroethyl ether

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