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.

    1276/1290 (page 1256)
    C,H,,0,N,;8, 2) 4-Amidoazobenzol-3,4’-Disulfonsäure. Ba-+ 71/,H,O (B. 15, 2187). — IV, 1370. | C,H,,0,NCl, 1) Acetylimid d. ««öö- Tetrachlor-ßy-Diacetoxylbutan-$y-Dicarbon- säure. Sm. 176—177° u. Zers. (A. 254, 104). — I, 1405. C,H,O,NS, 1) #-Amido-4-Oxybiphenyl-2,2’-Disulfonsäure. Ba 7®)H,0 (A. 261, 315). — II, 896. C,H,,0,N,Br 1) Aethylester d. f-Keto-«-[Brom-2,4-Dinitrophenyl]propan-«-Car- bonsäure (Ae. d. Bromdinitrophenylacetessigsäure). Sm. 96°. Na (Am. 12, 167). — II, 1659. C,H,,N,C1S 1) ?-Chlor-2-[@-Phenylhydrazonäthyljthiophen. Sm. 108° u. Zers. (B. 19, 694). — III, 762. C,H,,N,BrS 1) 5-Brom-2-[«-Phenyihydrazonäthyljthiophen. Sm. 122° u. Zers. (B. 19, 689). — III, 763. C,H,,N,JS 1) 5-Jod-2-[«-Phenylhydrazonäthyljthiophen. Sm. 134° u. Zers. (B. 19, 692). — III, 763. C,H,,N,SP 1) Phenylamid-Phenylimid d. Thiophosphorsäure (Sulfophosphazo- benzolanilid. Sm. 202° (B. 28, 1241). C,H,ONCI 1) 2-Chlor-5 oder 7-Oxy-4-Methyl-3-Aethylehinolin. Sm. 227° (B. 31, 2151). “2) 2-Chlor-4-Oxy-8-Methyl-3-Aethylchinolin. Sm. 225—225,5° (B. 21, 301). — IV, 335. 3) Chinolylacetonylchlorid. 2+-PtCl,, + AuCl, (C. 1899 [1] 117). -4) Isochinolylacetonylchlorid.. 2+ PtCl,, + AuCl, (A. 303, 118). C,H,ONBr 1) Aethyläther d. 6-Brom-l-Amido-2-Oxynaphtalin. Sm. 84° (0.1897 1] 239). 2) ei ehinolin. Sm. 126—127° (B. 31, 2373). ‚CsH,ONJ 1) 4-|P-Jod-?-Oxypropyljchinolin. Sm. 117—119° (B. 31, 2374). C,H,ON,;,S 1) 4-Keto-2-Phenylimido-3-Allyltetrahydrothiazol? Fl. (Soc. 71, 632). C,H,O0,NC1 1) Chlormethylat d. 2-Methylchinolin-3-Carbonsäure. Sm. 230° u. Zers. (A. 282, 127). — IV, 352. 2) Phenylimid d. y-Chlor-$-Methylpropan-fy-Dicarbonsäure (uns- Dimethylchlorsuceinanil). Sm. 163° (A. 295, 75). C,H,0,NCl, 1) Z£L-Triehlor-y-Oximido-s-Oxy-«-Phenyl-«o-Hexen (Benzylidenaceton- oximchloral). Sm. 113—114° (@. 28 [2] 86). ©,H,,0,NBr 1) Isobutyläther d. ?-Brom-2-Oxy-3-Ketopseudoindol (m-Bromisatin- | “isobutyläther) (5. 15, 2097). — II, 1606. 2) Bromäthylat d. Chinolin-4-Carbonsäure. Sm. 237° (A. 270, 358 Anm.). — IV, 347. C,H,0;NJ 1) Jodäthylat d. Chinolin-4-Carbonsäure + H,O. Sm. gegen 200° u. Zers. (207— 208° wasserfrei u. Zers.) (A. 270, 352; M. 15, 434). — IV, 346. C,H,0,NP 1) Phenylmonamid d. Phenylphosphinsäure. Sm. 125° (4. 293, 217). — IV, 1651. C,H,O,N,Br,1) Diäthyläther d. ?P-Dibrom-3-Oximido-2-Oxypseudoindol (D. d. Di- - bromisatoxim). Sm. 115—116° (B. 16, 1709). — II, 1612. C,H,0;N,S 1) ?-Diamidodiphenylsulfon. Sm. 168%. 2HCI, (2HCI,PtCl,) (2. 9, 80; | 14, 2184; A. 100, 212). — II, 814. 2) Diphenyldiamid d. Schwefelsäure (D. 24, 362). — II, 356. 3) 2-Amidophenylamid d. Benzolsulfonsäure. Sm. 168°. HCl (4. 221, 17; B. 16, 596). — IV, 561. 4) Phenylhydrazid d. Benzolsulfonsäure. Sm. 148—150° u. Zers. Na (4. 190, 132; B. 8, 1007, 10, 1531; 18, 894; 20, 1239). — IV, 738. C,H,O0,N,S, 1) 3-Amidophenylester d.3-Amidobenzol-l-Thiolsulfonsäure (3-Amido- phenyldisulfoxyd). 2HÜCl, 2HBr (A. 278, 255). — II, 818. C,H,O;NC1 1) Monomethyläther d. 4-Chlor-5,5-Dioxy-2-Keto-3-Methyl-l-Phe- nyl-2,5-Dihydropyrrol (Chloreitrakonanilmonomethyläther). Sm. 114° (A. 295, 62). 2) Chlormethylat d. Tarkonin. 2+PtCl,, 4+AuC], (A. 245, 321). — III, 918. 3) Chlormethylat d. Chininsäure. Sm. 215° (A. 276, 268). — IV, 362. C,H,,O,NBr 1) Bromeotarnin 4 H,O. Sın. bei 100°. (2HC1,PtCl,), HBr-+ H,O (Soe. 32, 531). — III, 917. 2) Aethylbromtarkoninsäure 4 2H,0. Sm. 223—225° u. Zers. Ba, Cu, (2HCI, PtCl,) (A. 212, 182). — III, 920.