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.

    1280/1290 (page 1260)
    C,,H,,0,N,Br 3) Acetylderivat d. Verb. C,,H,,0,N,Br (aus 6-Bromopiansäureamid). Sm. 242° (B. 31, 927). C,H,0,N;8% 1) 4-Amido-4- Hydrazidobiphenyl- 2,2'-Disulfonsäure.. Ba 4H,0 (A. 261, 319). — IV, 1169. A. 215, 235). — IV, 1412. C.H,N,C1Si 1) Verbindung (aus Anilin u. Silieiumchloroform) (C. 1896 [1] 803). C,H,‚,ONC1 1) Chlormethylat d. 6-Oxychinolin-6-Aethyläther+H,0. Zers. oberh. 200° (J. pr. [2] 56, 443). 2) Chlormethylat d. 8-Oxychinolin-8-Aethyläther 4 2H,0. Sm. 107° (J. pr. [2] 54, 14). — IV, 274. C,H, ONBr ]1)1- [2-Brombenzoyl]hexahydropyridin. Fl. (B. 21, 2251). — IV, 2. 2) 1-4-Brombenzoyljhexahydropyridin. Sm. 95° (B. 21, 2249). — IV, 13. > 3) P- -Brompropylamid d. B- -Phenylakrylsäure. Sm. 79—80° (B. 24, 3226). — IL, 1407. 4) y-Brompropylamid d. #-Phenylakrylsäure. Sm. 74° (B. 24, 3226). — II 1407. ‚5) ?-Brom-1,2,3,4-Tetrahydro-5-Naphtylamid d. Essigsäure. Sm. 1519,(3521 1895). — II, 587. C,H.,ONJ 12)J odmethylat d. 4-Oxy-2- Methylcehinolin-4-Methyläther. Sm. 201° (B. 22, 76; 30, 925). — IV, 311. 2) J odmethylat d. 6- Oxychinolin- 6-Aethyläther 4 H,0. Zers. bei 195—197° (J. pr. [2] 56, 442). 3) Jodmethylat d. 8- Oxychinolin-8-Aethyläther. Sm. 200° (J. pr. [2] t 54, 14). — va 274. x 4) Jodmethylat d. 7-Oxyisochinolin-7-Aethyläther. Sm. 193— 194° (A. 286, 15). — IV, 303. Hi. odäthylat d. 7-Oxyisochinolin-7- Methyläther. Sm. 178—179° (A. 286, 14). — IV, 308. C,H.,ON,Br, 1) Dibrommethyleytisin. HCl, (@HCI, PtCl), HBr (0. 1897 [2] 555). C,H,,ON,Br, 1) 2,4, 6,2',4',6-Hexabromazoxybenzol. Sm. 215° u. Zers. (B. 31, 564). hydroimidazol. Sm. 165° (B. 24, 3282). — II, 544. hydroimidazol. Sm. 175° (B. 24, 3284). — II, 472. 3) 2-Thiocarbonyl-5-Keto-4,4- Dimethyl- 1-[4- -Methylphenyl] tetra- hydroimidazol. Sm. 85° (£. 24, 32584). — II, 500. 4,5-Dihydroimidazol. Sd. 222—225°. Hcı, (2HCI, PtCl,), Pikrat (B. 24, 3295). — II, 404. 5) Dimethyläther d. 2. Merkapto-5-Oxy-4-Methyl-l- Phenylimidazol. Sm.:90°. HCl, (2HÜI, PtCl,), Pikrat (B. 24, 3290). — II, 404. 6) 2- Aethylimido- 4-Keto-5-Methyl-3- Phenyltetrahydrothiazol (Methyläthylphenylthiohydantoin).. Sm. 101° (DB. 31, 137). 7) 2-[2-Methylphenyl]imido-4-Keto- 5-Aethyltetrahydrothiazol. Sm. 95— 96,5%. HCI1 (Soc. 71, 636). 8) Amid d. 5-Keto-2-Methyl-1-Phenyltetrahydropyrrol-2#Thiocar- bonsäure. Sm.-193° u. Zers. (B. 22, 2368). — II, 419. C,H,,0;NC1 1) Chlormethylat d. 4,6-Dioxy-2-Methylchinolin-6-Methyläther. Sm. 251°. (2 + PtCl, + 4H,0) (B. 21, 1653). — IV, 312. C.,H,,0,NCl, 1) Acetat d. P6-Trichlor-«-Oxy-«-|?-Dimethylamidophenylläthan. Sm. 84—85° (B. 18, 1518). — II, 1064. C,H,,0,NBr 1) Brommethylhydrohydrastinin. Sm. 187° (B. 24, 2739). — IV, 203. 2) Acetat d. «-Oximido-«-|?-Brom-3,4-Dimethylphenylläthan. Sm. 109—110° (Soc. 63, 81). — III, 151. C.H,,0,;NJ 1) Jodmethylat d. 4,6-Dioxy-2-Methylehinolin-6-Methyläther (DB. 21, 1652). — IV, 312. 2) Jodmethylat d. ?-Dioxychinolindimethyläther. Sm. 210— 212° (DB. 20, 1826). — IV, 288. C,H,,0,NBr 1) Bromhydrocotarnin. Sm. 76—78°. (2HC1, PtCl,), HBr (Soc. 32, 531). — III, 908. 2) Aethyläther d. 2-Brom-4-Diacetylamido-l-Oxybenzol. Sm. 90° (B. 30, 480).