Previous Page PART 27 (65:X)-, (66)-, AND (X :66:X) -CHROMOPHORES system compound solv \nax loge ref no 65.C-6 1-benzylideneindene H 238 280 340 4.2 M50 4.3 4.3 4096 65:c-c:c-6 1-cinnamylideneindene H 245 297 371 4.3 M50 4.3 4.8 4097 66 naphthalene A 220 275.5 301 5.0 Dl 3.8 2.5 4098 H 221 275.5 302 5.2 M51 3.9 2.5 4099 267 360 4.5 H92 4.3 4100 naphthalene picrate C-66 C2-66 1-me thy !naphthalene H 220.5 281 322 5.0 M51 3.7 1.6 4101 -methy !naphthalene H 221 275 319 5.0 M51 3.7 2.5 4102 , 2-dimethy !naphthalene 10 228 285.5 322 5.1 3.8 2.9 F49 4103 , 3-dime thy !naphthalene 10 227 283 322 5.1 3.8 2.7 F49 4104 , 4-dime thy !naphthalene 10 227 288 4.9 3.8 F49 4105 , 5-dime thy !naphthalene 10 227 286.5 5.1 4.0 F49 4106 , 6-dime thy !naphthalene 10 226 282 322 5.1 3.8 3.0 F49 4107 , -dime thy !naphthalene 10 227 280 322 5.1 3.8 2.7 F49 4108 , 8-dime thy !naphthalene 10 229 285 322 5.0 3.9 2.0 F49 4109 system compound solv max loge ref no , 3-dime thy !naphthalene 10 226 278 320 5.2 3.8 2.5 F49 4110 ,6-dimethy !naphthalene 10 227 274 324 5.1 3.7 3.0 F49 4111 , 7-dime thy !naphthalene 10 226.5 277 321 5.1 3.7 2.4 F49 4112 , 2-trimethy lenenaphthalene A 227 280 323 5.0 3.7 3.4 M23 4113 acenaphthene A 228 289 321 4.9 3.8 3.2 J25 4114 , 2- tetr amethy lenenaphthalene ; 1,2,3,4tetrahydrophenanthrene cH 230 280 322 5.0 3.8 3.4 F49 4115 , 3-tetramethylenenaphthalene ; 1,2,3,4tetrahydroanthracene cH 230 276 386 4.9 3.7 3.7 F49 4116 , 8- trimethylenenaphthalene ; , 3-dihydro-lH-phenalene A 229 289 4.7 3.7 F49 4117 1,3, 5- t rime thy !naphthalene H 231 289 324 5.3 4.0 2.9 M51 4118 1,3, 8-trime thy !naphthalene H 231.5 285 326 5.1 3.8 3.2 M51 4119 1,6, 7-trimethy !naphthalene H 230 284 5.1 3.9 M51 4120 l,4-dimethyl-5-(l-carboxyethyl) naphthalene A 233 294 4.8 3.9 F49 4121 , 6-dime thy 1-4-isopropy !naphthalene H 232 284 325 5.0 3.9 3.3 M51 4122 C4-66 1,2,3,6,7, 8-hexahydropy rene Hp 234 296 5.0 3.9 F51g 4123 C6-Se l,2,3,3a,4,4a,5, 6,7,9,10,11-dodecahydro- A dibenzo [ cd ,mn] pyrene 242 295 335 5.0 4.0 3.6 C59 4124 C3-66 compound system N-66 no 241 297 330 5.0 4.0 3.4 F51g 4125 1-naphthylamine A 242 320 4.0 3.7 S65 4126 *1 220 277 4.9 3.8 S65 4127 *2 296 4.3 S65 4128 A 237 281 338 4.8 3.8 3.3 S65 4129 *1 220 275 4.9 3.7 S65 4130 complex of 1-naphthylamine with m-dinitrobenzene 242 320 362 4.6 3.8 3.0 H92 4131 complex of 2-naphthylamine with m-dinitrobenzene 237 276.5 338 4.9 4.0 3.4 H92 4132 A 305 3.7 S65 4133 *1 220 280 4.9 3.8 S65 4134 A 240 282 345 4.6 3.8 3.0 S65 4135 *1 219 275 5.0 3.7 S65 4136 1-acetamidonaphthalene M 286 S2g 4137 2-acetamidonaphthalene M 240 280 312 S2g 4138 2-benzamidonaphthalene cH S2g 4139 l-(o-carboxybenzamido) naphthalene M S2g 4140 2- (dimethylamino) naphthalene *2 ref Hp 1- (dimethylamino)naphthalene 0.01N HC1/W loge l,2,2a,3,4,4a,5,6,6a,7,8,8a,9,10-tetradecahydrocoronene 2-naphthylamine *1 solv \nax 0.01N NaOH/W 226 ^298 222.5 290 4.6 4.1 system compound solv \nax NC2-SS 5-ethanethionamidoacenaphthene M 228 275 300 AsN-SS l-aminonaphthalene-2-arsonic acid M 224 248 318 0-66 1-naphthol A 220 290 *1 10.0 *1 acid A ref no S2n 4141 S2g 4142 4.6 3.7 F49 4143 233 295.5 323 4.5 3.7 3.4 Dl 4144 245 331.5 4.3 3.8 Dl 4145 A 228 275 330 4.8 3.7 3.3 F49 4146 cH 226 273 328 4.8 3.7 3.4 F49 4147 *1 226 274 330 4.9 3.7 3.3 Dl 4148 1-methoxynaphthalene cH 231 293 4.6 3.8 F49 4149 2-methoxynaphthalene A 227 271-2 328 4.9 3.6 3.3 S30 4150 1-acetoxynaphthalene A 221 280 312 4.9 3.8 2.3 Dl 4151 2-acetoxynaphthalene A 221 274 317 4.9 3.7 2.5 Dl 4152 , 2-dihydroxynaphthalene *1 234 290 334 4.7 3.6 3.4 Dl 4153 10.0 235 345 4.2 3.2 Dl 4154 2-naphthol 02-66 loge 4.2 3.5 3.5 system compound , 4-dihydroxynaphthalene , 5-dihydroxynaphthalene solv ^max 244 334 4.2 3.7 Dl 4155 10.0 267 4.0 Dl 4156 *1 226 299 4.9 3.9 Dl 4157 10.0 225 330 4.6 4.0 Dl 4158 S2g 4159 M 228.5 280.5 325.5 ,6-naphthalenediol A 228 260 349 4.9 3.7 3.4 Dl 4160 *1 229 260 269.5 349 4.8 3.7 3.7 3.4 Dl 4161 230 350 4.6 3.4 Dl 4162 A 232 285.5 328 4- 3.5 3.4 Dl 4163 *1 232 285.5 328 4.9 3.5 3.4 Dl 4164 10.0 239 282 340 4.7 3.6 3.5 Dl 4165 *1 245 315 4.6 3.7 Dl 4166 10.0 265 330 460 4.4 3.4 3.5 Dl 4167 222 333 347.5 4.7 3.9 3.9 Dl 4168 260 350 4.0 3.2 Dl 4169 1,2,4-naphthalenetriol 1,4, 5-naphthalenetriol *1 10.0 acid A no , 3-naphthalenediol , 7-naphthalenediol *1 ref *1 10.0 03-66 loge system compound 2,3, 6-naphthalenetriol solv OC-66 OC2-66 02C-66 *1 acid A loge ref no A 239 282 331 4.5 3.4 3.3 Dl 4170 *1 239 282.5 331 4.6 3.4 3.3 Dl 4171 243 284 331 4.5 3.5 3.4 Dl 4172 10.0 04-66 max 2-acetoxy-l, 4-naphthalenediol *1 244 323.5 4.5 3.8 Dl 4173 5-acetoxy-l , 4-naphthalenediol *1 226 305 322 4.7 3.9 3.9 Dl 4174 1,2,4, 5-naphthalenetetrol *1 282 350.5 403 4.0 3.4 2.8 Dl 4175 1,3,4, 5-naphthalenetetrol *1 280 345 400 3.9 3.4 2.8 Dl 4176 4-methyl-l-naphthol C 303 3.8 E2 4177 3- (hydroxymethyl) -2-naphthol M 227.5 275.5 329 S2g 4178 A 6-methoxyestra-l, , (10) , , 8-pentaen-17one 240 303 4.6 3.8 J13 4179 1,2,3, 4- tetrahydro-7-methoxy-2-methyl1, 2-phenanthrenedicarboxylic acid monomethyl ester A 238 277 331 4.7 3.8 3.3 Bl 4180 2-methy 1-1, 4-naphthalenediol *1 245 265.5 324.5 4.5 3.4 3.7 Dl 4181 2-acetoxy-4-methyl-l-naphthol C 294 328 3.8 3.4 E2 4182 , 2-diacetoxy-4- (acetoxymethyl)naphthalene A 226 283 4.9 3.9 E2 4183 system O3C-SS ON-SS S-SS S2-SS *1 acid A compound solv max loge ref no , 7-dimethoxy-2-methyl-l-naphthol 236 288 298 333 4.7 3.8 3.8 3.5 S23 4184 7-dimethoxy-3-methyl-l-naphthol 233 284 295 342 4.8 3.9 3.9 3.6 S23 4185 , 8-dimethoxy-3-methyl-2-naphthol A 235 302 335 4.7 3.7 3.6 E2 4186 5-amino-l-naphthol A 228 308 4.7 3.9 G31g 4187 8-amino-2-naphthol M 247.5 303 S2g 4188 5-acetamido-2-naphthol M ^227 288.5 337 S2g 4189 2-naphthalenethiol iO 225 241 280 336 4.6 4.6 3.9 2.9 F49 4190 1-naphthalenesulfonic acid *1 224 283 315 4.8 3.8 2.6 Dl 4191 2-naphthalenesulf onic acid A 227 274.5 320 5.0 3.7 2.6 Dl 4192 *1 227 275 320 5.0 3.7 2.6 Dl 4193 1,5-naphthalenedisulfonic acid *1 227 283 318 4.8 4.0 2.9 Dl 4194 2,7-naphthalenedisulfonic acid A 233 266 315 3.5 3.6 2.4 Dl 4195 *1 232.5 266.5 315 5.0 3.6 2.4 Dl 4196 compound system solv 10.0 SO-66 Dl 4197 *1 284 3.8 B80n 4198 *2 317 3.8 B80n 4199 *3 237 317 324 4.3 3.9 3.9 BSOn 4200 4-acetamido-l-naphthalenesulfonic acid *4 227 297 S2g 4201 l-hydroxy-2-naphthalenesulfonic acid *5 237 294 328 4.6 3.6 3.6 Dl 4202 4-hydroxy-l-naphthalenesulfonic acid *5 234 300 4.5 3.9 Dl 4203 5-hydroxy-l-naphthalenesulfonic acid *5 241 311.5 4.5 3.7 Dl 4204 l-hydroxy-6-naphthalenesulfonic acid *5 245 304 334 4.6 3.5 3.5 Dl 4205 2-hydroxy-l-naphthalenesulfonic acid *5 229 278 330 4.8 3.7 3.4 Dl 4206 2-hydroxy-6-naphthalenesulfonic acid *5 233 280 332 4.9 3.7 3.1 Dl 4207 S2g 4208 , 3-dihydroxy-6-naphthalenesulf onic acid M S20-66 2-hydroxy-3, 6-naphthalenedisulf onic acid *1 *5 0.98M HC1/W acid A 238.5 281 330 *5 237 273 342 4.9 3.6 3.2 Dl 4209 2-hydroxy-6 , 8-naphthalenedisulf onic acid *5 237 287 338 4.8 3.8 3.5 Dl 4210 S2g 4211 l-amino-8-hydroxy-2 , 4-naphthalenedisulfonic acid *2 no 5.0 3.6 2.5 S02-66 S2ON-66 ref 231 266.5 315 4-amino-l-naphthalenesulfonic acid SN- 66 max loge 0.001M HC1/W *3 W 0.0001M NaOH + 0.5M NaCl/W 237 340 *4 Na salt in M system compound solv max loge ref no 1-fluoronaphthalene PE 279 3.8 F14 4212 2-f luoronaphthalene PE 270 3.8 F14 4213 1-chloronaphthalene PE 283 3.8 F14 4214 2-chloronaphthalene PE 276 3.8 F14 4215 1-bromonaphthalene PE 285 3.9 F14 4216 2-bromonaphthalene M 277 S2g 4217 1-iodonaphthalene PE 287 4.0 F14 4218 2-iodonaphthalene PE 279 3.9 F14 4219 1,1 '-binaphthyl A 228 282 294 4.6 4.1 4.1 F50 4220 l,2T-binaphthyl A 219 226 292 4.8 4.8 4.2 F50 4221 , f -binaphthyl A 212 254 305 4.7 5.0 3.3 F50 4222 C-66-66 , 2f -binaphthyl-1-ylacetic acid A 250 4.8 F49 4223 C-66-66-C dibenzo[a,g] f luorene A 255 285 349 4.8 4.1 4.3 FIl 4224 C2-66-66-C2 , 2f , , ' -tetramethyl-1 , f -binaphthyl A 228 284 319 5.1 4.0 3.1 F50 4225 N-66-66-N , 2f -diamino-1 , f -binaphthyl A 241 282 346 5.0 4.1 3.8 J25 4226 *1 285 4.1 J25 4227 A 218 280-90 5.1 4.0 05 4228 F-66 Cl-66 Br-66 1-66 fiC—fifi oo~oo 0-66-66 1f -hydroxy-1 , 2f -binaphthyl 02-66-66-02 , ' , , 7f -tetrahydroxy-1 , f -binaphthylA 232 303 5.0 4.0 B112 4229 A , 3f , , ' -tetraacetoxy-1 , f -binaphthyl 288 4.1 B112 4230 *1 IN HC1/W system compound solv ^max loge ref no 66-c:c 2-viny !naphthalene C 247 284 4.7 4.2 LOn 4231 66-0.'C-C 1-propeny !naphthalene H 293 4.0 P7g 4232 l-(3-hydroxy-l-butenyl) naphthalene A 228 296 4.7 4.0 B117 4233 2-(3-hydroxy-l-butenyl)naphthalene A 246 284 4.7 4.2 B117 4234 2-isopropeny !naphthalene A 238 283 296 4.7 4.1 4.1 F49 4235 1- (l-cyclopentenyl)naphthalene A 225 295 4.7 3.9 Big 4236 1- (l-cyclohexenyl)naphthalene A 225 281 4.5 3.9 F49 4237 234 320 348 4.4 3.9 3.7 B81 4238 66-9:0 C 66-0:0-0 C 0-66-0:0-0 phenalene; perinaphthindene 00-66-9:0-0 6-methoxyestra-l ,3,5 (10) ,6,8, 14-hexaen17-one A 259.5 302 330 4.7 J13 3.9 3' 4239 0-66-0:9-66-0 4c , 14-dihydrodibenzo [ de ,mn] naphthacene A 270 303 400 4.7 4.9 4.5 036 4240 66-0:0-0:0-66 l,4-di(l-naphthyl)-l,3-butadiene D 240 292 362 4.4 3.7 4.3 H67 4241 1- (1-naphthyl) -4- (2-naphthyl) -1 , 3-buta- D diene 238 276 364 4.6 4.4 4.6 H67 4242 , 4- (di-2-naphthyl) -1 , 3-butadiene D 240 282 356 4.5 4.6 4.9 H67 4243 , T -azonaphthalene A 214 266 400 4.9 4.3 4.2 B30 4244 , 2? -azonaphthalene A 216 264 381 4.8 4.3 4.2 B30 4245 C 66-N.'N-66 system compound solv ^max loge ref no 1,3 -dime thy If luoranthene A 242 290.5 352 368 4.7 4.5 4.0 4.0 S78 4881 , 3-dimethylf luoranthene A 241 293 350 366 4.7 4.4 3.9 4.0 S78 4882 C3-S3S 1, 2, 3-trimethylf luoranthene A 243 292.5 352 367 4.7 4.5 4.0 4.0 S78 4883 N-S3S 1-aminof luoranthene A 225 259 285 327 393 4.6 4.6 4.2 4.0 4.0 F49 4884 1- (ethoxycarbonylamino) f luoranthene A 248 288 331 360 4.6 4.5 4.0 3.9 F49 4885 1-methoxyf luoranthene A 246.5 285.5 372 4,7 4.4 4.0 S78 4886 3-methoxyf luoranthene A 240 296 363.5 4.7 4.6 4.1 S78 4887 7-methoxyf luoranthene A 222 246 290 352 363 4.6 4.3 3.7 4.1 4.1 S78 4888 8-methbxyf luoranthene A 236 295 344 361 4.6 4.6 3.7 3.8 S78 4889 f luoranthene-1-carbonhydrazide A 238 289 328 350 362 4.6 4.4 3.9 3.9 3.9 F49 4890 ethyl f luoranthene-1-carboxylate A 244-73 285-95 329 359-75 4.5 4.3 3.9 3.8 F49 4891 C2-S3S 0-S3S 63s-c:o N S3S-CiO system compound solv max loge ref no 635: c-c :o benzo [a] f luoren-11-ylidenesuccinic acid A 263 293 314 344 4.8 4.2 4.0 3.2 F49 4892 63s : N-N benzo [a] f luoren-11-one 2,4-dinitrophenylhydrazone D 256 415 3.7 3.4 F49 4893 benzo [a] f luoren-11-one semicarbazone A 242 308 352-67 4.6 4.1 3.9 F49 4894 S3SiN-O benzo [ a] f luoren-11-one oxime cH 260-8 286 298 318 360 4.6 4.5 4.5 3.6 3.5 F49 4895 635:0 benzo [a] f luoren-11-one A 268 372 4.8 3.5 03 4896 benzo [b] f luoren-11-one A 284 339 415 4.9 3.6 3.0 03 4897 benzo [ c ] f luoren-7-one A 291 336 425 4.7 3.3 3.0 03 4898 c2-635: o , 6-trimethylenebenzo [b] f luoren-11-one A 292 352 435 4.8 3.7 3.4 F49 4899 o:63s:o f luoranthene-2 , 3-quinone D 261 4.7 F49 4900 64 triphenylene A 257 5.2 F49 4901 chrysene A 220 267 319 360 4.6 5.1 4.2 3.0 C58 4902 benzo [c]phenanthrene A 218 281 315 350 4.7 4.9 4.1 2.6 C58 4903 pyrene A 241 272 333.5 4.9 4.6 4.7 C51 4904 benz[ a] anthracene A 220 286 340 384 4.7 5.1 3.9 2.9 M23 4905 system C-S4 compound solv max loge ref no naphthacene A 278 416 444 474 5.1 3.6 4.0 4.1 F49 4906 1-methylchrysene A 269 323 362 5.1 4.2 2.9 F49 4907 2-methylchrysene A 269 321 361 5.2 4.0 2.4 F49 4908 3-methylchrysene A 269 321 362 5.1 4.1 2.9 F49 4909 4-methylchrysene A 271 327 366 5.1 4.0 2.8 F49 4910 5-methylchrysene A 266 325 367 5.1 4.0 2.9 F49 4911 6-methylchrysene A 269 324 362 5.2 4.1 3.0 F49 4912 1-methy Ibenzo [ c ] phenanthrene A 222 287 320 362 4.5 4.7 4.0 2.5 F49 4913 2-methylbenzo [ c ] phenanthrene A 283 357 375 4.9 2.7 2.7 B17 4914 3-methylbenzo[c] phenanthrene A 283 356 373.5 4.9 2.5 2.3 B17 4915 4-me thy Ibenzo [ c ] phenanthrene A 285.5 357.5 374.5 4.8 2.5 2.2 B17 4916 5-methylbenzo [c]phenanthrene A 220 283.5 356.5 374.5 4.6 4.9 2.6 2.4 F49 4917 6-methy Ibenzo [ c ] phenanthrene A 283.5 359 377 4.8 2.6 2.4 B17 4918 compound system solv max logc ref no 1-me thy lpy rene A 242 274 343 5.0 4.8 4.7 F49 4919 -me thy lpy rene A 243 274 336 5.0 4.6 4.7 F49 4920 4-me thy lpy rene A 241 274 336 4.9 4.7 4.6 F49 4921 1-methylbenz [a] anthracene A 287.5 341 387.5 4.9 3.9 3.2 J19 4922 2-methylbenz [a] anthracene A 226 291 342.5 388 4.6 4.9 3.9 3.2 BIl 4923 -me thy Ib en z [a] anthracene A 224-30 289 343.5 385.5 4.5 4.9 3.8 2.7 BIl 4924 4-methy Ibenz [a] anthracene A 293 344.5 388 5.0 3.9 3.0 BIl 4925 5-me thy Ibenz [ a] anthracene A 224 291 340.5 388 4.6 5.0 3.9 3.1 BIl 4926 6-me thy Ibenz [a] anthracene A 224 288.5 342 385 4.6 5.0 3.8 3.2 J19 4927 -me thy Ibenz [ a ] anthracene A 222.5 291.5 354.5 389.5 4.5 5.0 3.9 3.1 J19 4928 8-methylbenz [ a] anthracene A 225.5 289 346 386 4.5 4.9 3.9 3.1 J19 4929 -me thy Ib en z [ a] anthracene A 224 289 343.5 385 4.5 4.9 3.8 2.5 BIl 4930 system C2-S4 compound solv max loge ref no 10-methylbenz[ a] anthracene A 224-50 288.5 340.5 387.5 4.5 5.0 3.8 3.2 BIl 4931 11-methylbenz [a] anthracene A 232 290 346 386.5 4.6 4.0 3.9 3.1 J19 4932 12-me thy lbenz[ a] anthracene A 223 290.5 351.5 4.4 4.9 3.9 J19 4933 5-methylnaphthacene A 277 449 480.5 5.4 3.9 4.0 C36 4934 , 5-dimethylchrysene A 274 330 345 5.1 4.3 4.3 J21 4935 , 6-dimethylchrysene A 220 274 322.5 333 374.5 4.6 5.0 4.1 4.1 2.8 J21 4936 , 5-methylenechrysene A 269 301 326.5 360 5.0 4.1 4.1 2.9 J21 4937 (l-methylbenzo[c]phenanthr-4-yl) acetic acid A 224 290 326 4.6 4.8 4.0 F49 4938 , 8-dimethylbenzo [ c] phenanthrene A 221 286 321 4.6 4.9 4.0 F49 4939 , 7-tr imethylenebenzo [ c ] phenanthrene A 287 301 321 383 4.8 4.2 4.0 3.1 C58 4940 , 7-dimethylpyrene A 246 277 338 378 5.0 4*7 4.7 3.0 F49 4941 , 2-tetramethylenepyrene A 247 280 346 378 4.9 4.6 4.6 3.2 K47n 4942 system C3-S4 compound solv max loge ref no , 12-dimethylbenz [a] anthracene A 278 287 341 387 4.9 4.9 3.9 3.1 C14 4943 3-isopropyl-7-methy Ibenz [a] anthracene A 294 353 390 5.0 3.9 2.6 J20 4944 7, 8-dime thy Ibenz [a] anthracene A 294.5 358 392.5 4.9 4.0 3.2 J19 4945 , 11-dime thy Ibenz [a] anthracene A 295 356 391.5 5.0 4.0 3.1 J19 4946 , 12-dimethylbenz [ a] anthracene A 296.5 364 4.9 4.9 J19 4947 8, 11-dimethy Ibenz [a] anthracene A 292.5 352 386.5 4.9 3.9 3.1 J19 4948 l,12-methylenebenz[a]anthracene A 256.5 289 350.5 387 4.6 4.7 3.9 3.5 J19 4949 cholanthrene A 220 284 296 358 4.6 4.8 4.9 3.9 F49 4950 8, 9-trimethylenebenz[ a] anthracene A 225 293 352 4.6 4.0 3.8 F49 4951 , 10-trimethylenebenz [a] anthracene A 224 288 345 386 4.6 5.0 3.9 3.2 F49 4952 , 6-dimethylnaphthacene A 278 433 454 5.3 3.8 3.9 F26 4953 1,7, 8-trimethylchrysene 274 315 329 367 5.1 4.2 4.2 2.7 R43 4954 7-methyl-l , 12-methylenebenz [a] anthracene B A 292 357.5 4.7 3.9 J20 4955 system C4-S4 compound solv max loge ref no 3-methylcholanthrene A 220 284 297 359 4.5 4.8 4.9 3.7 F25 4956 ll~methylcholanthrene A 286 297.5 360 4.8 4.9 4.0 J20 4957 1,2,7, 8-tetramethylchrysene 275 335 369 5.1 4.1 2.9 D7n 4958 , , 2a , , , 4a , , 6-octahydrocoronene Hp 247 281 349 383 4.8 4.7 4.7 3.5 F49 4959 , 11-dimethylcholanthrene A 287 298 360.5 4.9 5.0 3.9 J20 4960 ,11-dimethylcholanthrene A 288 298.5 360 4.8 4.8 3.8 J20 4961 , 10 : ,4-di (trimethylene)pyrene A 248 281.5 351.5 383 4.9 4.8 4.5 3.5 C36 4962 ^6-64 1,2,5,6,9, 10-hexahydrocoronene A 273 302 344 5.0 4.4 3.2 F49 4963 N-S4 1-aminopyrene A 242 284.5 ^362.5 4.6 4.4 4.2 J25 4964 241.5 274 339 4.9 4.6 4.6 J25 4965 *1 *1 2N HCl/50% A 2-aminopyrene A 266 338.5 ^4OO 4.8 4.5 3.2 J25 4966 5-aminobenz [ a] anthracene A 292.5 365 4.5 3.9 J20 4967 *1 289.5 344 4.9 3.8 J20 4968 system compound 7-aminobenz[ a] anthracene *2 no 4.5 4.6 3.9 J20 4969 H 259.5 302.5 383 405 4.5 4.7 3.9 4.0 J20 4970 *1 289.5 351.5 370 4.8 3.9 3.7 J20 4971 A 267 395 4.9 3.9 J25 4972 *1 289.5 347 387 4.9 3.8 3.0 J25 4973 7-acetamidobenz [a] anthracene A 291 351 388 5.0 3.9 3.1 B8 4974 6-hydroxychrysene A 225 272 322-32 373 4.6 5.0 4.0 3.5 F49 4975 1-hydroxypyrene A 241 278 348 386 4.8 4.5 4.3 4.0 J25 4976 *2 245 287 ^408 4.6 4.4 4.3 J25 4977 *3 250 337 384 4.8 4.7 3.4 F49 4978 *4 273 344 ^408 4.3 4.5 3.5 F49 4979 4.6 4.6 4.1 F49 4980 *5 2N HCl/50% A 2N NaOH/50% A ref 259.5 302.5 405 2-hydroxypyrene *1 *5 max loge A 8-aminobenz [a] anthracene 0~64 solv 0.5N NaOH/50% A *3 0.01N HCl/50% A *4 275 315.5 436.5 IN KOH/50% A system O2-S4 *1 IN NaOH/50% A compound solv max loge ref no 4-hydroxypyrene A 241 281 343 378 4.7 4.3 4.2 3.5 F49 4981 5-hydroxybenz [a] anthracene A 288 338 407 4.7 3.9 3.3 J20 4982 *1 296 368.5 432.5 4.6 4.0 3.5 J25 4983 1-methoxypyrene A 241 278 346 382 4.8 4.6 4.4 4.0 J25 4984 4-methoxypyrene cH 244 280 346 373 4.8 4.5 4.4 3.5 F49 4985 5-methoxybenz [a] anthracene A 285 334.5 395 4.8 3.9 3.3 J20 4986 7-methoxybenz [a] anthracene A 280 291 336 353 371 4.9 5.0 3.8 3.9 3.8 J25 4987 12-methoxybenz [a] anthracene A 288 352 389 4.9 3.9 3.2 B8 4988 7-acetoxybenz [a] anthracene A 279 290 333 350 387 4.9 5.0 3.9 4.0 2.9 B8 4989 12~acetoxybenz[ a] anthracene A 277 287 334 344 389 4.9 4.9 3.8 3.9 3.2 B8 4990 , 12-dimethoxybenz [a] anthracene A 281 293 362.5 4.9 4.9 3.8 B8 4991 system compound solv max loge ref no , 12-diacetoxybenz [a] anthracene A 279 289 339 355.5 368 391 4.9 4.9 3.9 3.9 3.9 3.2 B8 4992 5-methoxy-10-methylbenz [a] anthracene A 278 290 343 360 402 4.7 4.8 3.9 3.9 3.4 J20 4993 8-methoxy-7-methylbenz [a] anthracene A 287.5 298 V367 4.7 4.7 3.9 F49 4994 12-methoxy-7-methylbenz [a] anthracene A 282 293 361 4.9 4.9 4.0 J25 4995 l-acetoxy-4-methylbenzo [ c ] phenanthrene A 221 277 286 4.6 4.6 4.8 D25 4996 2-acetoxy-4-methylbenzo [ c ] phenanthrene A 220 278 286 317 4.6 4.7 4.8 4.1 D25 4997 7-acetoxy-12-methylbenz[ a] anthracene A 282 293 359 4.9 4.9 4.0 B8 4998 OC2-S4 9-methoxy-3-methylcholanthrene A 294 348 401 4.9 3.8 3.6 J25 4999 S-S4 7-thiocyanatobenz [a] anthracene D 296.5 362.5 4.9 3.9 J22 5000 12-thiocyanatobenz [a] anthracene D 302 379.5 405 4.9 4.2 4.2 J22 5001 chrysene-6-sulfonic acid D 5.0 4.1 4.1 F49 5002 4.7 4.7 4.2 J22 5003 OC-S4 SC-S4 7-methyl-12-thiocyanatobenz [a] anthracene D 276 V321 V333 275 311 415.5 system compound solv max loge ref no 1-chloropyrene H 242 275 343 5.0 4.7 4.8 F39n 5004 9-chlorobenz [a] anthracene cH 292 331 347 385 5.1 3.9 3.9 2.9 F49 5005 9-chloro-7-methylbenz [ a ] anthracene A 295 356 5.1 3.9 F49 5006 10-chloro-7-methylbenz[ a] anthracene A 224 294 349 392 4.5 5.0 3.9 3.2 F49 5007 ClC3-S4 9-chloro-5-methylcholanthrene A 296 362 398 4.9 3.8 3.6 J25 5008 Br-S4 7-bromobenz[ a] anthracene A 292.5 355.5 391 5.2 4.0 4.0 B8 5009 BrC-S4 7-bromo-12-methylbenz [a] anthracene A 296 364 4.9 4.0 B8 5010 BrC2-S4 8-bromo-7 ,12-dimethylbenz [a] anthracene A 300 372 4.9 4.0 J25 5011 6-isopropenylchrysene A 222 269.5 310 323.5 363 4.5 5.1 4.1 4.1 2.9 J23 5012 C-S4-CiC-C , 8-dihydrobenzo [a] pyrene A 247 254 280 292 347 364 4.6 4.6 4.4 4.5 4.5 4.6 K47n 5013 C-S4-CiC-C 7-methyl-9 ,10-dihydrobenzo [a]pyrene A 281 345 378 399 4.8 4.5 3.0 2.9 F49 5014 S4-CiN 1-cyanopyrene A 244 279 351 382 4.8 4.7 4.7 4.0 F39n 5015 Cl-S4 ClC-S4 V^c system C-S4-CiN C3-S4-CiN S4-CiO C-S4-CiO «t° C-S4Hp: o compound solv max loge ref no 7-cyanobenz [ a ] anthracene A 295 375 396 4.8 3.9 3.8 B8 5016 7-cyano-12-methylbenz [a] anthracene A 296 378 4.8 4.0 B8 5017 8-cyano-7-methylbenz[ a] anthracene A 226 240 288 300 380 400 4.5 4.5 4.8 4.9 3.9 3.8 F49 5018 10-cyano-7-methylbenz [a] anthracene A 288 298 366 4.9 5.0 3.9 F49 5019 9-cyano-3-methylcholanthrene A 262 308 368 4.6 4.9 3.8 J25 5020 ll-cyano-3-methylcholanthrene A 249 310.5 356 425 4.5 5.0 3.9 3.7 J25 5021 1-pyrenecarboxaldehyde Hp 233 287 363 372 391 4.6 4.6 4.4 4.4 4.4 J25 5022 benz [a] anthracene-7-carboxaldehyde A 249 303 403.5 4.6 4.7 3.9 J25 5023 12-methylbenz[a]anthracene-7-carboxaldehyde A 294.5 386 4.7 4.0 B8 5024 6-acetylchrysene A 225 270 335 4.6 4.8 4.1 J23 5025 3- (l-carbonylpyrene)propionic acid A 233 242 281 352 4.6 4.6 4.4 4.3 J25 5026 7,8,9, 10-tetrahydro-7-oxobenzo [a] pyrene A 277 327 343 415 4.8 4.3 4.6 3.2 F49 5027 compound system solv max loge ref no C2- 64-c: o 3-methyl-l~oxocholanthrene A 234 308 386 4.6 4.7 4.0 J25 5028 n-o N- (benz [a] anthracene-5-carbonyl) glycine 8.3 292 343.5 4.7 3.9 J20 5029 N-(benz[a]anthracene-7~carbonyl)glycine 8.0 290 352 4.9 3.8 J20 5030 5-chrysenecarboxylic acid *1 220 270 311 350 4.5 5.0 4.1 3.0 J25 5031 benzo[c]phenanthrene-6-carboxylic acid A 221 285 368 385 4.6 4.8 2.9 2.9 F49 5032 1-pyrenecarboxylic acid C 283 352 385 4.5 4.5 4.1 F39u 5033 2-pyrenecarboxylic acid C 265 339 395 4.9 4.6 3.3 F39u 5034 benz [a] anthracene-7-carboxylic acid A 291 349 387 4.9 3.9 3.1 B8 5035 7-cholanthrenecarboxylic acid H 265 285 297.5 362.5 4.7 4.7 4.8 3.9 F49 5036 *2 264 271 287 296 362 4.6 4.6 4.7 4.7 3.9 J25 5037 *3 266 286 298 363 4.6 4.8 4.8 3.9 J25 5038 A 296 351 390 4.8 3.8 3.5 B8 5039 T C2-64-C.'0 : °f benz[a]anthr~7-ylglyoxalic acid *:>r-n *1 0.05N HC1/A *2 0.01N HC1/A *3 0.5N NaOH/50% A system *r compound solv max loge ref no 6-nitrochrysene A 260 363-71 4.7 3.9 F49 5040 7-nitrobenz [a] anthracene A 288 350 387.5 4.7 3.8 3.5 B8 5041 5-isocyanatobenz [a] anthracene H 286.5 297 346 4.9 4.9 4.9 J20 5042 7-isocyanatobenz [a] anthracene H 294 361 380.5 5.0 4.0 4.0 J20 5043 64-6 12-phenylbenz [a] anthracene A 290 345 389 5.1 4.0 3.4 C60 5044 C-S4-S-C 8H-dibenzo[def ,qr]chrysene A 296 349 378 399 5.1 4.9 3.9 4.0 C49 5045 S""~64~~6 , 12-diphenylbenz [a] anthracene A 294.5 357 4.8 4.1 B8 5046 X* 5,6, 11-triphenylnaphthacene B 295 445 473 505 5.0 3.6 3.9 4.1 B12 5047 5,6, 11-tri (p-tolyl)naphthacene B 296 445 473 506 5.1 3.8 4.1 4.1 B12 5048 'I*- 5-phenoxy-6 , 11 , 12-triphenylnaphthacene B 299 460 490 525 5.0 3.8 4.1 4.1 B12 5049 X4 5,6,11, 12-tetraphenylnaphthacene ; rubrene B 303 465 495 530 5.1 3.8 4.1 4.1 B12 5050 ?>