Amines. 



768 



1630 



Ethylideneaniline 



/S-NlTRiVETim.IDENE ANIL 



NOj.CHj.CH : XPh 

 Meister, W. B., 40, (3435). 



Methylenedianiline C,3Hi4N2 

 CeH5.XH.CH2.XH.CsH5 



^,J:^ '-Dimethyl and 'S,K' -diethyl 

 derivatives. 

 Fromicli, E. B.. 40, (762). 



Ethylenedianiline CjjljeXj 



i.e. CeHj.XH.CH^.CH^.XH.CeHs 

 ^,^'-Di7nethyl and diethyl derivatives. 

 FrohUch, E. B., 40, (762). 



Trimethylenedianiline C^.R^.K^ 



i.e. C6H5.XH.[CH,]3.XH.C6H5 

 FrbhUch, E. B., 40, (762). 



Benzylidene aniline C6H5.X : c;HPh 



Clarke A Lapworth. [Condensation 

 of benzylideneaniline hydrocyanide ^vith 

 carvone and with benzv'lideneaceto- 

 phenone. The compound, C27H23X3, 

 fonr.ed by the union of two mols. of 

 benzylideneaniline with one mol. of 

 hydrogen cyanide.] J.C., 91, (694). 



Mayer. Condensation de la benzyli- 

 dene-aniline avec I'ether acetone dicar- 

 bonique. Bl., 33. (49Sj. 



Diphenylamine XHPhj 



0, m and p-nitrodiphenylamines. 

 Goldberg, J. B., 40, (4541). 



NiTRO DERIVATIVES 



[2:4: 6]C6H2(X02)3.XfT.C6H,.XO, [2'] 



and [4'J XH(C,H,.X02)2 [2 : 2'] ; 



[2] X02.CeH,.XH.CeH3(N02)2 [2' : 41 



and [2: 4 :^6J CeH2fN02)3.XH.C6H3(NOj)2 



[2' : 4']. Also the 7iit7-osamines 



[2]and[4]C6H,fX02).X7XO).C6H4.XO, 



[2'] and [4'] 



Juillard. BI., 33, (1172). 



Hexanitrodiphextlamine. 

 Aleksandrov. Les sels et les ethers 

 du bexanitro-diphenvlamine. (Russe) 

 Z., 39, (1391). 



DiphenyljJmine 

 2,2' ; 2,3' and 2,4'- dicarroxylic acids. 



2-OxYDIPHENYLAMINE 2-CARBOXYLIC AOID. 



Ullmann, Fr. A.. 355, (312). 



Triphenylamine XPhj 



Goldberg u. Nimerovsky, M. B., 40. 

 (2448). 



AMINES C7HgN 

 o-Toluidine CHj.CgH^.XHj [1 : 2J 



lODOACETYL, OIILOROACETYL, DICHLORO- 

 ACETYI. and TRICHLOROACETYL DERIVATIVES. 



Bodroux. Bl., 35, (519). 



a-IODOPROI'IONYL and a-IODO-)i-HUTYRYL 

 DERIVATIVES. 



Bodroux et Taboury, F. C.R., 144, 



(1437;. 



loDO-o-TOLClDIKE 



Cn3.CeH3I.XH2 [1:3:6] 

 and its acetyl derivative. 

 Artmann, F. M., 26, 1091). 



m-Toluidine- 



Teltscher. Einwirkuncr von Aether 

 und Alinniniunichlorid anf ui-Toluidin. 

 Diss. Heidelberg, 1906. 



lODO-m-TOLCIDINE 



CH3.CeH3I.XH2 [1:2:5] 

 and its acetyl derivative. 

 Artmann, P. M, 26, (1091). 



pTolaidine. 



Kurbatov. Chaleur latente de I'eva- 

 poration du paratoluidiiie. (Russe 1 Z., 

 39, (Pr.-verb. 1144). 



MOSOHYDRATE. 



Walker & Beveridge. Par«-Tolui- 

 dine monobydrate. J.C, 91, (1797). 



AteTVL DERIVATIVE. 



Coben e^ Cross. 45224. Mechanism 

 of bromination of acylamino-compounds. 

 [Bromination of aceto-jMoluidide.] 



3-CHL0R0-5-RR0M0-p-T0LriDiNE and its 

 acetyl derivalive. 



Orton & Reed, W. W. J.C, 91' 

 (1554). 



Phenyl-p-toluidine Ci3H,3X 



(i-Tolylaniline). 

 Goldberg, J. B., 40, (4541). 



Benzylamine C5H5.CH2.XH2 



Phenylbenzylmethylethyl- 



ammonium salts. 



Jones. 47893. Resolution of opti- 

 cally active ammonium salts by mean*] 

 of tartaric acid. 



