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Ethyl o-toluidine

Chemical Name N-ethyl-N-(2-methyiphenyi)-2-butenamide Common Name Crotonyi-N-ethyl-o-toluidine... [Pg.395]

Ethyl p-toluenesulfonate Bretylium tosylate N-ethyl o-toluidine Crotamiton Ethyl undecylenate lophendylate Ethyl urethane Mebuta mate 170 -Ethynyl estradiol Quinestrol... [Pg.1634]

N-Ethylpiperidine, 43,45 Ethyl-o-toluidine, 43,47 Ethyl trichloroacetate for generation of dichlorocarbene, 41, 76... [Pg.114]

Ethy Ibenzy lamine A -Methyl o-toluidine A -Methyl m-toluidine. 2V-Methyl p-toluidine A -Ethyl o-toluidine -Ethyl m-toluidine -Ethyl p-toluidine 2V-Methyl a-naphthylamine 2V-Methyl p-naphthylamine 2V-Phenyl- a-naphthylamine N-Phenyl- p-naphthylamine... [Pg.659]

V-Ethylbenzylamine A -Methyl o-toluidine TV-Methyl m-toluidine. A7-Methyl p-toluidine A7-Ethyl o-toluidine A7-Ethyl m-toluidine A7-Ethyl p-toluidine A7-Methyl a-naphthylamine. . ZV-Methyl p-naphthylamine. 2V-Phenyl-a-naphthylamine. N-Phenyl- p-naphthylamine. ... [Pg.659]

Chemical Name N-Ethyl-N-(2-methylphenyl)-2-butenamide Common Name Crotonyl-N-ethyl-o-toluidine Structural Formula ... [Pg.1140]

V-ethyl-o -toluidine. ( I I,C,I I,NI K l f. Properties Colorless to yellowish oil. D 0.9534 bp 214C. Soluble in alcohol, ether, and hydrochloric acid insoluble in water. Combustible. Derivation Heating ethanol with o-toluidine and hydrochloric acid. [Pg.542]

Beilstein Handbook Reference) Aniline, 2-methyl-6-ethyl- Benzenamine, 2-ethyl-6-methyl- BRN 2079468 C 25702 EINECS 246-309-6 2-Ethyl-6-methylaniline 6-Ethyl-2-toluidine 6-Ethyl-o-toluidine 2-Methyl-6-ethylaniline o-Toluidine, 6-ethyl-. [Pg.625]

Methylaniline Ethylaniline n-Propylaniline n-Butylaniline Benzylaniline AT-Methylbenzylamine N -Ethy Ibenzy lamine AT-Methyl o-toluidine M-Methyl m-toluidine iV-Methyl p-toluidine Al-Ethyl o-toluidine N-Ethyl TO-toluidine N-Ethyl p-toluidine A -Methyl a-naphthylamine A -Methyl p-naphthylanaine A -Phenyl- a-naphthylanaine Af-Phenyl- p-naphthylamine... [Pg.1231]

During recent years, Sharma and coworkers (88-90) have been able to find examples of dissociation ext-ration which have distinct features and are truly remarkable. Firstly, they have illustrated that the use of a diluent may be avoided advantageously (89). This is particularly relevant for every sparingly water soluble organic acids/bases and, here, apart from the difference an ionisation constants, the relative solubilities of species (rather than the distribution coefficients) play an important role. Typical examples are mixtures of N-ethyl-o-toluidine and NN -diethyl-o-toluidine where higher values of the separation factors are obtained without a solvent (4,89). [Pg.604]

Ethyl-o-toluidine (2-Me yl-i.. ylaniline, -amino-1 -meOiyl- -ethylbemene)... [Pg.56]


See other pages where Ethyl o-toluidine is mentioned: [Pg.875]    [Pg.354]    [Pg.1144]    [Pg.338]    [Pg.1054]    [Pg.251]    [Pg.816]    [Pg.1378]    [Pg.384]    [Pg.1141]    [Pg.1141]    [Pg.215]    [Pg.1378]    [Pg.207]    [Pg.395]    [Pg.103]    [Pg.56]    [Pg.196]    [Pg.263]    [Pg.1753]   
See also in sourсe #XX -- [ Pg.43 , Pg.47 ]

See also in sourсe #XX -- [ Pg.43 , Pg.47 ]




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