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.

    1282/1290 (page 1262)
    C,H,;0,N,C1 1) ?-Chlor-?-Dinitro-5-Pseudobutyl-l, 3-Dimethylbenaol, (0. 1897 [1] 783). ar C,H,,0,N;Br 1) ?-Brom-?-Dinitro-5- Pseudobutyl-1, 3-Dimethylbenzol. Sm. 730 f 3 (0. 1897 [1] 783). I C,H,,0,N,J 1) ?-Jod-?-Dinitro-5-Pseudobutyl-1,3- Ditmetbripehanı Sr 105 (©. 1897 [1] 783). ER C.,H,,;0,NS 1) 1,2-Diäthylester d. Benzol-1,2-Diearbonsäure-3- Sulfonsäureamid. A Sm. 101,5—102° (Am. 13, 198). — II 1824. * C,H ,O0,N;,S 2 Alloxandimethylanilindisulfit En AH, O (A. 248, 148), - — II, 328. be C,H,,;N,JS 1) Methyläther d. 2-Merkapto-l- [4-Methylphenyl]imidazol-3- -Jod- methylat. Sm. 162° (B. 25, 2364). — IV, 508. ee C.,H,ONCL, 1) $$$-Trichlor-«- Oxy-«-[?P-Diäthylamidophenylläthan. Fl. HCl v (5. 19, 368). — II, 1064. u. C,H ,„ONBr ]) 1-[5-Brom-2- Oxybenzyl] hexahydropyridin. Sm. 63—64 (A. 302, > US Sg 2) Methylphenylamid d. «-Bromisovaleriansäure. Sd. 160—163%, h (B. 31, 3240). u Be 3) 2-Methylphenylamid d. «-Bromisovaleriansäure. Sm..125° (B.8L, U 3237). a | 4) 3-Methylphenylamid d. «-Bromisovaleriansäure. Sm. 135° (B. 31, 3237). TE 5) 4-Methylphenylamid d. «-Bromisovaleriansäure. Sm. 124° (B. 31, I BRBUN.: ie Mi 6) Benzylamid d. «-Bromisovaleriansäure. Sm. 98° (B. 31, 3236). 7) Aethylphenylamid d. «-Brombuttersäure. Fl. (B. 30, 3180). 48) Aethylphenylamid d. «-Bromisobuttersäure, Sm. 8080, 50 (B. 30, x 3180). Sm. E32 9) 2,4-Dimethylphenylamid d. «-Brombuttersäure. Sm. 145° (B. 3l, “ 3 3237). 10) 2,4- Dimethylphenylamid &; «-Bromisobuttersäure. Sm. 103P(B: 31, 3237). 11) ?-Brom-4-Isobutylphenylamid d. Essigsäure. Sm. 1530 ie 21, f 2941). — IL, 557. er C,H,ON,S 1) s- Valerylphenylthioharnstoff. Sm. 98— 990 (Soe. 67, 1041). | 2) = RU SE 2-Methylphenylthioharnstoff. Sm. 136— -1370 (Sr. Br 9,7863). # Ei 3) S- rer 4- Methylphenylthioharnstoff. Sm. 134—135° (Soe. 0 69, 864). 4) u -Benzoylimido- a - Diäthylamido - « - Merkaptomethan (Benzoyl- a, pseudodiäthylthioharnstoff). Sm. 100—101° (Soc. 69, 1603). - > 5) Phenylamid d. 2,4-Dimethyltetrahydrooxazol-3- Thiocarbonsäure A (Dimethyloxazolidylphenylthioharnstoff‘) Sm. 145° (B. 30, 2257). C,H,ON,S 1) Nithialin. Zers. bei 200° (A. 96, 115). — IV, 578. C,H, 0; NCl 1) Chlormethylat-6, 7- Methylanäther d. 6,7- Dioxy-2- Methyl-1,2, 3 ‚d- j Tetrahydroisochinolin. 2 + PtCl, (B. 24, 2736). — IV, 202. we C,H,,0,NJ 1) Jodmethylat-6, 7-Methylenäther d. 6, 7-Dioxy-2- Methyl- 1,2,3,4- = Tetrahydroisochinolin. Sm. 2972280 (B. 24, 2735). — IV, 202. 2) Jodmethylat d. Homohydroeinchoninsäure + H,O (M. 5, 649. — IV, 215. BR C,H,,0;N,S Aethylester d. a-[2,4- Dimethylphenyljthioharnstoff-$-Carbon- _ säure. Sm. 152,5—158° (Soc. 69, 329). ‚a C.H,O;N;8S, 1) Diäthylester d. 1,3- Phenylendi[amidothioameisensäure], Sm. 116° Br (B. 20, 230). — IV, 576. . 2) Diäthylester d.1 ‚4-Phenylendi[amidothioameisensäure). Sm. 1 sa (B. 20,230). — IV,'592, a C3H50,N.B.) Verbindung (aus Acetylphenyldithiourazol). Sm. 195— 208° (B. 28, 957). C,H, 0;NBr 1) Aethyläther d. 6-Brom-2-Nitro-3-Oxy-4- Isopropyl-1-Methyl- benzol. Sm. 67—69° (G. 19, 64). — II, 773. 2) Brompropylat d. Chininsäure. Sm. 1920 (A. 276, 276). I 362. C,H, 0;N,S 1) 23,5-Dimethylbenzimidazol + Acetonsulfit (BD. 21, 1909). —_ IV, 880. C,H,O,NC1 1) Verbindung (aus d. 3,5-Dioxy-l- Methylbenzoxazoldiäthyläther) Sm. 82. B bis 85%; Sd. 201— 2020 (M. 18, 377). C,H,.0,NBr 1) Acetat d, n-Brom-e-Oximidocampher (Soc. 69, — III, 15