Download E-books Handbook of Ultraviolet and Visible Absorption Spectra of Organic Compounds PDF

By Kenzo Hirayama

This revised and enlarged model has been compiled to include tabulation in keeping with absorption maxima.

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2 three. four B97 1414 N-phenylmorpholine cH 248 284. five S2g 1415 me thy identity ipheny lamine A 245 291 three. nine four. 1 J5 1416 triphenylamine A 228 297 three. nine four. three J5 1417 4-amino-l , 2-dihydro-2 , 2-dimethyl-6(N-methylanilino) -1 , three , 5-triazine hydrochloride W 247 M43q 1418 four , 6-diamino-l , 2-dihydro-l , 2-diphenyl1,3, 5-triazine hydrochloride W 251 M43q 1419 N-ethyl-N-phenylurea A 235-7 three. five S30 1420 N , N f -diethyl-N-phenylurea A 239-41 270-3 three. 6 three. zero S30 1421 N , N , N! -tr iethy 1-N T -plienylurea A 252-4 3,9 S30 1422 N,N'-diethyl-N,N! -diphenylurea; diethylcarbanilide; centralite A 247 three. nine S30 1423 N , N-diphenylur ea A 242 four. 1 S30 1424 N, N-diethy 1-N ? ,N'-diphenylurea A 245-6 four. 1 S30 1425 tetraphenylurea A 266-7 four. three S30 1426 N-ethylformanilide A 232-4 three. nine S30 1427 N , N-dipheny If ormamide A 240 four. 2 S30 1428 N-butylacetanilide A 225 three. 7 B62u 1429 N, N-dipheny lace tamide M 266 four. 2 L20 1430 N,N! -diethyloxalanilide A 230-1 four. 1 S30 1431 N , N T -diphenyloxalanilide A 238-9 four. three S30 1432 ethyl N-ethyl-N-phenylcarbamate; ethylpheny trap than A 231 three. 7 S30 1433 ethyl N, N-dipheny lcarbamate; diphenylurethan A 238 four. 1 S30 1434 procedure compound solv. max. approach N2-6 compound max. loge ref. no. N,N-diphenylcarbamic anhydride A 236-7 four. four S30 1435 N,N,N-trimethylanilinium iodide A 259 2. 6 B97 1436 N-ethyl-N-nitrosoaniline A 270-3 three. eight S30 1437 N-nitrosodiphenylamine A 295-6 three. eight S30 1438 N,NT-diphenylhydrazine; hydrazobenzene A 285 four. zero L6u 1439 M 228 315 S2g 1440 tetraphenylhydrazine A 258-9 292-3 four. 2 four. three S30 1441 N-acetyl-NT-phenylhydrazine ; N f -phenylacetohydrazide M 234 280 four. zero three. zero S2g 1442 1-phenylsemicarbazide M 234 283 four. 1 three. zero S2g 1443 2-phenylsemicarbazide A 242 four. zero M67 1444 2-phenylthiosemicarbazide A 255 three. nine M67 1445 2-phenylselenosemicarbazide A 271 three. nine M67 1446 o-phenylenediamine A 237 293 three. nine three. 6 M56 1447 nine. zero 206 233 289 four. 6 three. eight three. five D35 1448 A 230 293 four. zero 2,5 S50 1449 nine. zero 210 289 four. 6 three. three D35 1450 *1 243 2. 1 S2g 1451 A 244 312 three. nine three. 2 A26 1452 *2 253 2. zero A26 1453 E 253 329 four. 2 three. five A26 1454 *2 255 2. three A26 1455 m-phenylenediamine p-phenylenediamine N-methyl-p-phenylenediamine *1 solv. dihydrochloride in M *2 5N/3 HC1/W system compound solv. max. loge ref. no. A 288 four. 2 A26 1456 *1 285 four. 1 S2g 1457 *2 287 four. 1 S2g 1458 *3 280 four. 1 A26 1459 o-aminoacetanilide A 290 three. five G23r 1460 m-aminoacetanilide A 295 three. four G23r 1461 p-aminoacetanilide A 259 four. 2 G23r 1462 N,N-dimethyl-p-phenylenediamine E 258 329 four. 2 three. five A26 1463 *4 254 2. four A26 1464 S2g 1465 N-phenyl-p-phenylenediamine N,N-diphenyl-p-phenylenediamine M ^245 302 bis [p-(dimethylamino)phenyl]amine A 321 four. 7 B155 1466 p-bis [bis (2-cyanoethyl)amino] benzene A 262 309 four. 2 three. three B123 1467 o-diacetamidobenzene A 278 three. zero G23r 1468 m-diacetamidobenzene A 233 285 293 four.

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