Volume 1

Lexikon der Kohlenstoff-Verbindungen / von M.M. Richter.

  • Max Richter
Date:
1900
Catalogue details

Licence: Public Domain Mark

Credit: Lexikon der Kohlenstoff-Verbindungen / von M.M. Richter. Source: Wellcome Collection.

    1283/1290 (page 1263)
    CoHis O,N,P, C,H,,ONS e C,H,,ONCI C,H ,ONJ C,,H,,0,NC1l C,H,O,NBr C,H .ONT C.H,;0;N,S, C.H,O0,N,;S ma — 12 IV. 1) Verbindung (aus Phenylhydrazin u. P,0,). Sm. 242—248° u. Zers. (A. 272, 213). — IV, 662. 1) Säure (aus Albumin) (A. 101, 193). — IV, 1583. 1) Aethyläther d. 2,4, 6-Trimethylphenylimidomerkaptooxymethan. ‚Sm. 88° (B. 15, 1015). — II, 555. 2) Diäthyläther d. 2-Methylphenylimidomerkaptooxymethan. Fl. (A. 207, 163). — II, 464. . 3) Diäthyläther d. 3-Methylphenylimidomerkaptooxymethan. Fl. (4. 207, 163). — II, 479. | 4) Diäthyläther d. 4-Methylphenylimidomerkaptooxymethan. Sd. oberh. 250° (B. 13, 1577; A. 207, 163). — II, 496. ? 5) Isoamylester d. Phenylamidothiolameisensäure. [2] 32, 249). 1) Jodmethylat d. 5-Keto-2,3-Dimethyl-1-Phenyltetrahydropyrazol. Zers. bei 310° (B. 26, 106). — IV, 489. 2) Jodmethylat d. Cytisin + 2H,0. Sm. 270° (B. 24, 677). — III, 879. 1) y-Phenylsulfonamido-f-Ketohexan. Sm. 97,8° (B. 28, 2043). 1) Aethyläther d. 5-Chlor-3,6-Di[Dimethylamido]-2-Oxy-l, 4-Benzo- ehinon. Sm. 90—91° (J. pr. [2] 43, 264). — III, 348. 1) Aethylester d. ?P-Chlor-4-Isopropyl-1-Propylbenzolsulfonsäure. Sm. 42—43° (@. 19, 503). — II, 153. 1) Verbindung (aus Leuein u. Benzolsulfonsäurechlorid). Sm. 86° (B. 23, 319%). — II, 115. 1) Phosphorigsaures 2-Nitrophenylhydrazin. Sm. 160° (B. 27, 2551). 1) 2-Methylphenylimid d. Piperidylthiophosphinsäure (Thiophos- phazo-o-Toluolpiperidid). Sm. 236° (B. 28, 1244). — IV, 12. 2) 4-Methylphenylimid.d. Piperidylphosphinsäure (Thiophosphazo- p-Toluolpiperidid). Sm. 257° (B. 28, 1246). — IV, 12. 1) Chlormethylat d. 8-Oxy-1-Methyl-1,2,3,4-Tetrahydrochinolin-8- Methyläther. 2 + PtCl, (B. 19, 1044). — IV, 199. 1) Aethyläther d: 2-Brom-5-Amido-3-Oxy-4-Isopropyl-1-Methyl- benzol. ‘Fl. 'HOC1 (@. 19, 335). — II, 774. 1) Jodmethylat d. 2-Oxy-1,3,3- Trimethyl-2,3-Dihydroindol. Sm. 165° u. Zers. (@. 27 [1] 476). — IV, 235. 2) Jodmethylat d. 6-Oxy-l1-Methyl-1,2,3,4-Tetrahydrochinolin-6- Methyläther + H,0. Sm. 223—224°. (2HCl, PtC1,) (M. 6, 779). — IV, 198. 3) Jodmethylat d. 8-Oxy-l1-Methyl-1,2,3,4- Tetrahydrochinolin-8- Methyläther. Sm. 175° (B. 19, 1043). — IV, 199. | l) Aethylester d. Dimethylphenylehlorammoniumessigsäure. 2-4 PtCl,) (B. 12, 2206). — II, 439. 2) Benzoat d. Trimethyl-$-Oxyäthylammoniumchlorid. 2 + PtCl],, — AuCl, (B. 27 [2] 738). — II, 1176. l) n-Brom-«-Acetylamidocampher. Sm. 167—168° (Soc. 69, 317), — III, 496. 1) Jodmethylat d. 2,4, 6-Trimethylpyridin-3-Carbonsäureäthylester. Sm. 128° (A. 225, 133). — IV, 150. 1) Diacetylderivat d. Dipropylenpseudohydrazodicarbonthioamid. Sm. 242° (B. 29, 862). l) Dextrosehydrazid d. Benzolsulfonsäure. Sm. 154—155°(B.28, 161). 1) Amid d. ?-Aethyl-tert.-Butylbenzol-?-Sulfonsäure. Sm. 98° (B. 27, 1613). 2) Amid d. 5-Pseudobutyl-1,3-Dimethylbena2ol-?-Sulfonsäure. 141—142° (B. 27, .1606). 3) Amid d. 1,3-Dipropylbenzol-?-Sulfonsäure. — II, 159, 4) Amid d. 1,4-Dipropylbenzol-2-Sulfonsäure. (@. 21, 26; Am. 5, 162). — II, 159. 5) Amid d. 1,2-Diisopropylbenzol-?-Sulfonsäure. 3144). — II, 160. 6) Amid d. 1,3-Diisopropylbenzol-?-Sulfonsäure. 3143). — II, 160. | 7) Amid d. 1-Propyl-4-Isopropylbenzol-«o-Sulfonsäure. .(@. 21, 17), — II, 160, Sm. 67° (J. pr. Sm. Sm. 195° (B. 24, 770). Sm. 106—107° (103% Sm..102° (B. 23, Sm. 145° (B. 23, Sm. 93—94°