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M-Phenylenebis

Fig. 9 Hiickel MO diagrams of diphenykarbene [15 m = 1], m-phenylenebis(phenylcarbene) [15 m = 2] and poly( i-phenylene-carbenes) [15],... Fig. 9 Hiickel MO diagrams of diphenykarbene [15 m = 1], m-phenylenebis(phenylcarbene) [15 m = 2] and poly( i-phenylene-carbenes) [15],...
Monomers not commercially available were prepared by known methods 4,4 -bis(p-aminophenyl)-2,2 -bithiazole (22), 2,5-bis(p-aminophenyl )oxadiazole (22), N,NMbis( p-aminophenyl )isophthalamide (27), 2V,N -m-phenylenebis(m-aminobenzamide) (23), and 1,4-bis(p-amino-phenyl) butadiene (16). Cuprous chloride was obtained by ascorbic acid reduction of CuCl2 according to Stathis (26). [Pg.697]

SYNS 1,3 -BIS-AMINOMETHYLBENZEN (CZECH) MXDA m-PHENYLENEBIS(METHYLAiMINE) m-XYLYLENDIAMIN (CZECH)... [Pg.1437]

PHENYLDIPHENYL see TBC750 PHENYL-DRANE see SPC500 N,N -(m-PHENYLENE)BISMALEIMIDE see BKL750 m-PHENYLENEBIS(METHYLAMINE) see XHS800 2,2 -(l,3-... [Pg.1836]

Other methods to prepare aromatic halo- or dihalo-phosphines are occasionally used. Arylbis(dialkylamino)phosphines have been converted into aryldihalophosphines with dry HCl or HBr, e.g. dichloro(2-methoxy- or 2-dimethylaminophenyl)phosphine (equation 29) the o- and m-phenylenebis(dichlorophosphine)s 20 and 21" and the p-phenylenebis(dichlorophosphine) 22. The c -phenylenebis(dibromophosphine) 23 has been prepared similarly Aryldiazonium tetrafluoroborates with PCI3 give chlorophos-phonium salts, which can be reduced to aryldichlorophosphines (equation 30). Primary and secondary phosphines may be chlorinated with phosgene to give chlorophosphines, e.g. hexamethylenebis[chloro(phenyl)phosphine] (equation 31) and 20 ". ... [Pg.10]

Synonyms/Trade Names 1,3-bis(Aminomethyl)benzene 1,3-Benzenedimethanamine MXDA m-Phenylenebis(methylamine) m-Xylylenediamine ... [Pg.337]

N-Phenyidiethanolamine. See Phenyidiethanolamine Phenyl diisodecyl phosphite. See Diisodecylphenyl phosphite 1-Phenyldodecane. See Dodecylbenzene m-Phenylenebis (methylamine). Seem-Xylylenediamine... [Pg.1271]

Synonyms 3-Aminomethyl benzylamine 1,3-Benzenedimethanamine Benzene-1,3-dimethaneamine 1,3-Bisaminomethylbenzene 1,3-Diaminomethylbenzene Methylamine, m-phenylenebis- MXDA m-Phenylenebis (methylamine) m-Xylenediamine m-Xylene-a,a -di-amine... [Pg.1421]

CAS 10114-58-6 EINECS/ELINCS 233-314-3 Synonyms Bismarck brown Bismarck brown Y Cl 21000 Excelsior brown Leather brown Manchester brown 4,4 -[1,3-Phenylenebis (azo)] bis]1,3-benzenediamine] dihydrochloride 4,4 -[m-Phenylenebis (azo)] bis [m-phenylenediamine] dihydrochloride Phenylene brown Classification Azobenzene Empiricai C18H20CI2N8... [Pg.393]

Synonyms 3-Aminomethyl benzylamine 1,3-Benzenedimethanamine Benzene-1,3-dimethaneamine 1,3-Bisaminomethylbenzene 1,3-Diaminomethyl benzene Methylamine, m-phenylenebis- MXDA m-Phenylenebis (methylamine) m-Xylenediamine m-Xylene-o,o -diamine Ciassification Aromatic amine Empincai C8H12N2 Formuia C6H4(CH2NH2)2 Properties Colorless to si. yel. clear liq. m.w. 136.20 dens. 1.032 vapor pressure 20 mbar (145 C) f.p. 14 C b.p. 245-248 C flash pt. > 112 C ref. index 1.5709 (20 C)... [Pg.4732]

Another vulcanizing agent for high-diene rubbers is m-phenylenebis-maleimide. A catalytic free radical source such as dicumyl peroxide or ben-zothiazyl disulfide (MBTS) is usually used to initiate the reaction. A reaction scheme for this type of vulcanization, adapted from Kovacic et al. [76] is as follows ... [Pg.351]

N,N -m-Phenylenebis (maleimide) polymers with benzalazine, 117 with 2-methyl-3,4-diphenyl-5- -propylcyclopentadienone, 114 with 6,6 - oxydi-p-phenylene)bis-(6-phenylfulvene), 118 with 6,6 -p-phenylenebis-(6-methyI ulvene), 102,118 with 2-vinylbutadiene, 107 N,N -o-Phenylenebis (maleimide),... [Pg.388]

See other pages where M-Phenylenebis is mentioned: [Pg.235]    [Pg.150]    [Pg.1029]    [Pg.235]    [Pg.150]    [Pg.318]    [Pg.851]    [Pg.965]    [Pg.965]    [Pg.195]    [Pg.345]    [Pg.1194]    [Pg.198]    [Pg.2580]    [Pg.3314]    [Pg.3314]    [Pg.967]    [Pg.345]    [Pg.967]    [Pg.94]    [Pg.94]    [Pg.148]    [Pg.437]    [Pg.404]    [Pg.416]    [Pg.118]    [Pg.119]    [Pg.119]    [Pg.384]    [Pg.387]    [Pg.394]    [Pg.789]    [Pg.260]    [Pg.150]   
See also in sourсe #XX -- [ Pg.337 ]



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