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1.1- dichlorodimethyl ether

Dichloro-2,2 -dihydroxy diphenylmethane, m243 1,1-Dichlorodimethyl ether, d237 Dichlorohydrin, d264... [Pg.175]

Dichlorodimethyl ether sym-Dichlorodimethyl ether. See Bis (chloromethyl) ether... [Pg.1261]

Addition of phosgene to the carbonyl group of a carboxylic ester, e.g. methyl formate, followed by elimination of carbon dioxide, generates 1,1-dichlorodimethyl ether (Chloromyl ) 1364, a liquid phosgene equivalent (bp 85 °C). Chloromyl is... [Pg.353]

Dichloroethyl formal, see Bis(2-chloroethoxy)methane Dichlorodiethyl methylal, see Bis(2-chloroethoxy)methane Dichlorodiisopropyl ether, see Bis(2-chloroisopropyl) ether sjm-Dichlorodimethyl ether, see sj jn-Dichloromethyl ether Dichlorodimethylhydantoin, see l,3-Dichloro-5,5-di-... [Pg.1475]

The parent system 1,3,4-oxadithiolane (12) was claimed to be formed on reacting a,a -dichlorodimethyl ether with sodium tetrasulfide in the presence of a base and subsequent steam distillation of the polymer obtained. However, since neither a structural proof nor any properties were described, the existence of this ring system should be considered in doubt (66HC(2l-l)l>. [Pg.887]

SYNS BCME BIS-CME CHLORO(CHLORO-METHOXY)METHANE DICHLORDIMETHYLAETHER (GERMAN) s) m-DICHLORODIMETHYL ETHER (DO T) sym-DICHLOROiMETHYL ETHER DIMETHYL-1,T-DICHLOROETHER OXYBIS(CHLOROMETHANE) RCRA WASTE NUMBER P016... [Pg.183]

DIHYDROXYDIPHENYLMETHANE see MJM500 DICHLORODIISOPROPYL ETHER see BII250 P,P -DICHLORODIISOPROPYL ETHER see BII250 DICHLORODIISOPROPYLSTANNANE see DNTOOO sym-DICHLORODIMETHYL ETHER (DOT see BIKOOO DICHLORODIMETHYLHYDANTOIN see DFE200... [Pg.1619]

DICHLORODIMETHYL ETHER or sym-DICHLORODIMETHYL ETHER (542-88-1) Forms explosive mixture with air (flash point <66°F/<19°C). Contact with water causes decomposition and the formation of hydrogen chloride. Forms unstable peroxides. Contact with oxidizers, peroxides, sunlight may form shock-sensitive compounds. Attacks many plastics, coatings. Flow or agitation of substance may generate electrostatic charges due to low conductivity. [Pg.399]

Beilstein Handbook Reference) BRN 0506943 CCRIS 138 Chlordimethylether Chlorodimethyl ether Chloromethoxymethane Chloromethyl methyl ether a,a-Dichlorodimethyl ether Dimethylchloroether EINECS 203-480-1 Ether, chloromethyl methyl Ether, dimethyl chloro Ether methylique monochlore HSDB 908 Methane, chloromethoxy- Methoxychloromethane Methoxy-methyl chloride Methyl chloromethyl ether Monochlorodimethyl ether Monochloromethyl methyl ether NSC 21208 RCRA waste number U046 UN1239, Liquid mp = -103,5° bp = 59.5° d = 1.063 soluble in EtOH, Et20, Me2CO, CHCI3. [Pg.133]

Synonyms/Trade Names BCME, bis-CME, Chloromethyl ether, Dichlorodimethyl ether, Dichloromethyl ether, Oxybis(chloromethane) ... [Pg.65]

The compounds 177 not yet ring closed to the cyclopropane may be synthesized by Lewis acid catalyzed addition of a-dichlorodimethyl ether to 4-methyl-3-pentene ester, (Reaction scheme 111) [261], to give ds/trans-caronaldehyde. [Pg.53]


See other pages where 1.1- dichlorodimethyl ether is mentioned: [Pg.191]    [Pg.348]    [Pg.353]    [Pg.617]    [Pg.344]    [Pg.344]    [Pg.617]    [Pg.619]    [Pg.441]    [Pg.191]    [Pg.2493]    [Pg.441]    [Pg.19]    [Pg.25]    [Pg.33]    [Pg.54]    [Pg.54]    [Pg.678]    [Pg.139]    [Pg.323]    [Pg.327]    [Pg.327]    [Pg.282]    [Pg.32]    [Pg.53]    [Pg.53]    [Pg.287]    [Pg.1017]    [Pg.348]    [Pg.758]    [Pg.491]    [Pg.353]    [Pg.617]    [Pg.315]    [Pg.206]   


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Dichlorodimethyl Ether (Chloromyl)

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