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3,5-Dimethylphenyl amine

N-Ethyl-(dimethylphenyl)- amine or N-Ethy -dimethylaniline and Derivatives (Xthyl-vic-o-xylidin in Ger),... [Pg.99]

N.N-Dimethylaniline or N,N-Dimethylphenyl-amine, CeH5.N(CH3)2. In this type, two methyl groups are attached to N of amino group... [Pg.223]

H2dnc (2-Pyridylmethyl)[(2-hydroxy-3,5-dimethylphenyl)methyl]- [2-hydroxy-5-methyl-3-(methylthio)phenyl)methyl]amine... [Pg.205]

Fig. 8.23. 3-(2-Acetoxy-4,6-dimethylphenyl)-3-methylbutanamides (8.188) as potential prodrugs of amines and peptides. Again, hydrolysis is followed by lactonization [240]. Fig. 8.23. 3-(2-Acetoxy-4,6-dimethylphenyl)-3-methylbutanamides (8.188) as potential prodrugs of amines and peptides. Again, hydrolysis is followed by lactonization [240].
Mononuclear complexes [U(C5Me5)2(NHR)2] (R = 2,6-dimethylphenyl, Et, or Bu) have been synthesized and structurally characterized. It was shown that in the presence of terminal alkynes and amines these complexes catalyze the intermolecular hydroamination of terminal alkynes [453]. Complex formation reactions of U(VI) with neutral N-donors in DMSO were reported [454]. [Pg.462]

Chemical Name 4H-l,3-Thiazine-2-amine, N-(2,6-dimethylphenyl)-5,6-dihydro-... [Pg.3489]

SYNS BAY 1470 BAY VA 1470 N-(5,6-DIHYDRO-4H-l,3-THIAZINYL)-2,6-XYLIDINE 2-(2,6-DIMETHYLANILINO)-5,6-DIHYDRO-4H-l,3-THIAZINE 2-(2,6-DIMETHYLPHEN i LAMINO)-4H-5,6-DIHYDRO-1,3-THIAZINE N-(2,6-DIMETHYLPHENYL)-5,6-DIHYDRO-4H-l,3-THIAZIN-2-AMINE N-(2,6-DIMETHYI,PHENYL)-5,6-DIHYDRO-4H-l,3-THIAZINE-2-AMINE (9CI) ROMPUN WH 7286 X l LAZINE (USDA) XYLZIN... [Pg.508]

N-(2,6-DIMETHYLPHENYL)-N-(METHOXYACETYL)-DL-ALANINE METHYL ESTER see MDMIOO N,N-DIMETHYL-3((1-PHENYLMETHYL)-1H-INDAZOL-3-YL)OXY-l-PROPAN AMINE HYDROCHLORIDE see BBW500 N-(2,6-DIMETHYLPHENYL)-l-METHYL-2-... [Pg.1648]

Local anesthetics make use of the lipophobic property of an aromatic amine moiety, or its acyl derivative, that links with a hydrophilic amino acid. The products include the anilide lidocaine, or 2-(diethylamino)-A-(2,6-dimethylphenyl)acetamide (153), the toluidine derivative prilocaine and the century-old procaine, 2-diethylaminoethyl 4-aminobenzoate (154)84. The ester is prepared by reacting p-aminobenzoic acid with ethylene chlorohydrin and diethylamine. [Pg.762]

Dimethylphenyl propionate, 162 Dimethy Iphcnylsilyllithium, 162-163 Dimethyl(phenylthio)aluminum, 163-164 Dimethyl(phenylthiomethyl) amine, 164 Dimethylsulfonium ethoxycarbonylmethyl-... [Pg.261]

Tp = tris(pyrazol-l-yl) borate Tp = tris(3,5-dimethylpyrazol-l-yl)borate TpR = substituted tris(pyrazol-l-yl)borate Tpx = general tris(pyrazolyl)borate TPA = tris(2-pyridylmethyl)amine tpy = 2-p-tolylpyridyl tren = tris(2-amino)ethylamine Trop = tropolonate Tu = thiourea Van = 4-vinylanisole Xyl = 2,6-dimethylphenyl... [Pg.544]

Deprotonation of (2,6-di-i-propylphenyl)(6-(2,4,6-tri-i-propylphenyl)p5 -din-2-yl)amine and (2,6-di-f-propylphenyl)(6-(2,6-dimethylphenyl)pyri-din-2-yl)amine using potassium hydride leads to crystalline organometallic polymers of type 1 (R = = z-Pr R = Me, R = H) where the aryl... [Pg.230]

In this extensive study of thiourea synthesis by coupling isothiocyanates with amines under mechanochemical conditions of neat and LAG, a total of 49 different thiourea derivatives were prepared. Since the supramolecular chemistry of simple synunetrical and nonsymmetrical diarylthiouieas had not previously been studied in detail, the information from the PXRD patterns of the milling products in this work also allowed for a systematic analysis of structural features of diarylthio-ureas. The three main self-assembly motifs were identified. A characteristic supramolecular synthon based on bifurcated N—H - S hydrogen bonds was found in most cases, whereby the individual thiourea molecules were assembled into chains aligned in a head-to-head (parallel molecular dipoles) or head-to-tail (antiparallel molecular dipoles) manner. In the case of slerically hindered thioureas, such as A -(2,6-dimethylphenyl)-A -phenylthiourea, the third motif arising from discrete cen-trosymmetric dimers based on rI(S) supramolecular synthon was found. A detailed look at the measured PXRD patterns for aU diarylthioureas revealed that solid-state structures of these compounds could be classified into two structural families, denoted as family I and family II (Fig. 1.11). [Pg.23]


See other pages where 3,5-Dimethylphenyl amine is mentioned: [Pg.605]    [Pg.531]    [Pg.111]    [Pg.336]    [Pg.271]    [Pg.451]    [Pg.100]    [Pg.1647]    [Pg.41]    [Pg.336]    [Pg.528]    [Pg.528]    [Pg.214]    [Pg.915]    [Pg.169]    [Pg.296]    [Pg.362]    [Pg.626]    [Pg.303]    [Pg.485]    [Pg.97]    [Pg.1590]    [Pg.1591]    [Pg.318]    [Pg.137]    [Pg.226]    [Pg.106]    [Pg.218]    [Pg.792]    [Pg.231]    [Pg.248]    [Pg.250]    [Pg.740]   


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3,5-Dimethylphenyl amine complexes

DIMETHYLPHENYL

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