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Previous Page PART 20 (6)(0:C)-SYSTEM ti system ^=O c-e-c:o N-SHJ: o o-e-c:o compound solv 4.0 L20 3131 N-me thy Ib enz amide M 223 4.0 L20 3132 N,N-dimethylbenzamide M 225 3.8 L20 3133 o-toluamide M 269 S2g 3134 m-toluamide M 257 S2g 3135 p-toluamide M 234.5 S2g 3136 N,N-diethyl-m-toluamide cH no S2g 3137 o- aminobenz amide M 213 248 S2g 3138 p-amino-N-ethylbenzanilide A 294-6 4.2 S30 3139 N-ethyl-p-(ethylamino)benzanilide A 306-7 4.2 S30 3140 p-aminohippuric acid M 280 S2g 3141 o-hydroxybenzamide 6.0 202.5 236 299 4.6 3.9 3.5 D35 3142 11.0 214.5 241.5 329 4.5 3.9 3.8 D35 3143 222 251 305 4.5 3.7 3.8 W4 3144 240-4 4.3 B45 3145 s-e-c:o p-carbamoylphenyl disulfoxide iil no 225 a-dihydroacetylcaranine lactam c-&-e-c:o ref M O2C-G-CiO o:c-6— c:o AtI * loge benzamide N TT0 TO max A N-phenylphthalimide A 294 3.3 F49 3146 N-ethyl-4 , 5-methylenedioxyphthalimide A 245 302 4.6 3.3 W4 3147 tetrachlorophthalimide A 234 330 3.9 3.4 R32 3148 tetrachloro-N- [ 2- (dime thylamino) ethyl ]'phthalimide A 288 R32 3149 2f -methylbiphenyl-2-carbonamide A no F49 3150 compound system c-^-.o f luorene-1-carbonamide e-c:c-c:o solv A max loge ref no 262 4.3 F49 3151 cis-cinnamamide 254 4.0 Pl 3152 trans-cinnamamide 273 4.3 Pl 3153 A 288 4.5 S80 3154 *1 288 4.5 S80 3155 *2 288 4.5 S80 3156 240 3.8 Pl 3157 N N-carbamoylcinnamamide ; cinnamoylurea w s ~i ' 2-phenyl-l-cyclohexene-l-carbonamide a- (p-chlorophenyl) -cis-cinnamamide A 292 4.4 C71 3158 a- (p-chlorophenyl) -trans-cinnamamide A 223 280 4.4 4.3 C71 3159 e-N:N-c:o carbamoylazobenzene A 223 286 434 4.4 4.5 2.6 F44 3160 Br-e-N:N-c:o l-bromo-4-(carbamoylazo) benzene A 245 300 440 3.8 3.9 2.1 F44 3161 6-N:N-6-c:s diphenylme thane thione E 315 620 4.2 1.8 B153u 3905 433.5 4.6 B155 3906 E 573 2.9 B155 3907 M 262 S2g 3908 A 353.5 579 4.5 2.6 B155 3909 E 592.5 2.6 B155 3910 H 344 596 4.5 2.6 B155 3911 cH 279 S2g 3912 , 5-diethyl-3 , 4-diphenyl-2 , 4-cyclopenta-10 dien-1-one 255 A17 3913 :> bis [p- (dimethylamino)phenyl]methanethione A bis(p-ethoxyphenyl)methanethione Ê>ôã 6-N:c:s &-s:ol-6 C2 phenyl isothiocyanate 4.3 PART 25 (X :6 :X)-CHROMOPHORES compound system O-N:S:N-O o-benzophenone oxime p-benzophenone oxime solv max loge ref no *1 398 3.8 G42 3914 *2 433.5 3.7 G42 3915 E 312 4.6 A21 3916 *1 317 4.4 G42 3917 *2 363 4.6 G42 3918 CI-N: e: N-CI N ,N T -dichloro-p-benzoquinonediimine E 303 314 4.6 4.6 A21 3919 C-N: e:N-c N ,N T -dimethyl-p-benzoquinonediimine dioxide M 385 4.2 P7 3920 N N -dicyclohexyl-p-benzoquinonediimine dioxide M 404 4.8 P7 3921 N,Nf-bis(l-cyanocyclohexyl)-p-benzoquinonediimine dioxide M 415 4.8 P7 3922 N-cyclohexyl-N T -phenyl-p-benzoquinonediimine dioxide C 415 4.6 P7 3923 N,NT-diphenyl-p-benzoquinonediimine dioxide C 423 4.6 P7 3924 M 272 338 417 4.6 4.6 4.7 P7 3925 O O c-iy:e:N-6 O O e-iy:6:N-6 O O 0-6-N:6:N-6-0 N , N f -bis (p-methoxyphenyl) -p-benzoquinonediimine dioxide C 431 4.6 P7 3926 ClC-6Hji:6:i}l-6-ClC O O N,NT-bis(3-chloro-o-tolyl)-p-benzoquinonediimine dioxide C 414 4.8 P7 3927 (N:S:N) (S)2(CXN)2 6 o N:S:N:N N- (2 , 4-dinitrophenyl) -N f -phenyl-p-benzo- C quinonediimine dioxide 408 4.5 P7 3928 1-diazo-l , 4-dihydro-4-iminobenzene W 254 357 3.8 4.5 A26 3929 *3 255 357 3.7 4.7 A26 3930 W 259 368 4.9 4.4 A26 3931 o l-diazo-l,4-dihydro-4-(methylimino)benzene *1 O IN H2S04/W *2 O IN NaOH/W *3 hydrochloride in W system compound solv max loge ref no *1 259 371 3.7 4.7 A26 3932 W 394 4.5 A26 3933 *2 248 376 3.8 4.6 A26 3934 1-diazo-l , 4-dihydro-4- (methy limino) benzene methochloride W 255 382 3.7 4.6 A26 3935 C2-N.'6:C-6-N p-benzoquinone-1- [p- ( dime thy lamino ) pheny lmethine ] -4-dimethylimmonium perchlorate *3 610 5.1 B139 3936 C2-N: e:c
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