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N-Methyl-m-toluidine

Methylaniline Ethylaniline n-Propylaniline n-Butylaniline Benzylaniline 2 -MethyIbenzylamine N-Ethylbenzylamine 2 -Methyl o-toluidine N-Methyl m-toluidine 2 -MethyI p-toluidine N-Ethyl o-toIuidine N-Ethyl m-toIuidine 2S -Ethyl p-toluidine 2 -MethyI a-naphthylamine N-Methyl p-naphthylamine N-Phenyl- a-naphthylamine 2 -Phenyl-P-naphthylamine... [Pg.659]

Of a series of indanylthiocarbamates, to1 indate (2) had significant antifungal properties. It is prepared simply from 5-indanyl thionochloroformate (1) by reaction with N-methyl-m-toluidine. It presumably joins the fairly large family of organic compounds having sulfur divalently bound to carbon which are useful topical agents for dermatophytes. [Pg.208]

Thiophosgene (1.15 g, 0.01 mol) in chloroform (40 ml) was slowly treated at room temperature with sodium l,4-methano-l,2,3,4-tetrahydro-6-naphthoxide (1.82 g, 0.01 mol). After 30 minutes, N-methyl-m-toluidine (2.42 g, 0.02 mol) in chloroform (40 ml) was added dropwise to the solution so obtained at room temperature. The reaction mixture was stirred for 48 hours at room temperature and then refluxed for 2 hours. The solvent was evaporated, and the residue redissolved in water and extracted repeatedly with diethyl ether. The organic phase was dried (Na2S04) and evaporated to... [Pg.3274]

Fig. 5.5. GC separation of TFA derivatives of arylamines. Peak 1 = solvent (CH2CI2) 2 = N-methyl-aniline 3 = N,N-dimethylaniline 4 = N-ethylaniline 5 = N-methyl-o-toluidine 6 = N-methyl-m-toluidine 7 = N-methyl-p-toluidine 8 = o-toluidine 9 = o-ethylaniline 10 = aniline 11 = 2,5-dimethyl-aniline 12 = 2,6-dimethylaniline 13 = 2,4-dimethylaniline 14 = m- toluidine 15 = p-toluidine 16 = 2,3-dimethylamline 17 = 3,5-dimethylaniline 18 = m-ethylaniline 19 = p-ethylaniline 20 = 3,4-dimethylaniline. Conditions stainless-steel column, 18 ft. X 0.125 in. O.D., 9.5% Apiezon L + 3.6% Carbowax 20M on Aeropack 30 (80—100 mesh) helium flow-rate, 100 ml/min column temperature, 152°C. (Reproduced from Anal. Chem., 39 (1967) 1188, by courtesy of the American Chemical Society.)... Fig. 5.5. GC separation of TFA derivatives of arylamines. Peak 1 = solvent (CH2CI2) 2 = N-methyl-aniline 3 = N,N-dimethylaniline 4 = N-ethylaniline 5 = N-methyl-o-toluidine 6 = N-methyl-m-toluidine 7 = N-methyl-p-toluidine 8 = o-toluidine 9 = o-ethylaniline 10 = aniline 11 = 2,5-dimethyl-aniline 12 = 2,6-dimethylaniline 13 = 2,4-dimethylaniline 14 = m- toluidine 15 = p-toluidine 16 = 2,3-dimethylamline 17 = 3,5-dimethylaniline 18 = m-ethylaniline 19 = p-ethylaniline 20 = 3,4-dimethylaniline. Conditions stainless-steel column, 18 ft. X 0.125 in. O.D., 9.5% Apiezon L + 3.6% Carbowax 20M on Aeropack 30 (80—100 mesh) helium flow-rate, 100 ml/min column temperature, 152°C. (Reproduced from Anal. Chem., 39 (1967) 1188, by courtesy of the American Chemical Society.)...
Other derivatives of 2-naphthol, less significant in terms of quantity, are the semi-synthetic penicillin nafcillin, and the antimycotic tolnaftate, which is produced from 2-naphthol, thiophosgene and N-methyl-m-toluidine Nippon Soda),... [Pg.321]


See other pages where N-Methyl-m-toluidine is mentioned: [Pg.69]    [Pg.1507]    [Pg.1508]    [Pg.211]    [Pg.717]    [Pg.1118]    [Pg.413]    [Pg.3274]    [Pg.401]    [Pg.401]    [Pg.401]    [Pg.1507]    [Pg.1507]    [Pg.1508]    [Pg.496]   
See also in sourсe #XX -- [ Pg.31 , Pg.38 ]

See also in sourсe #XX -- [ Pg.31 , Pg.38 ]

See also in sourсe #XX -- [ Pg.781 ]

See also in sourсe #XX -- [ Pg.781 ]

See also in sourсe #XX -- [ Pg.31 , Pg.38 ]

See also in sourсe #XX -- [ Pg.330 ]




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M-Toluidine

M-methyl-N-

Methyl toluidine

N-Methyl-3-toluidine

N-Toluidine

Toluidines

Toluidins

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