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.

    1284/1290 (page 1264)
    12 IV. CH, 0; 08° C,,H,90;N,J C,,H,0; NS C,H, BrIP C,H, NP C,H,„OCLP C,H,OJP C,H ,0,;NC1 C,H,O0,NJ C.,H,,0;NCl C.H;0;NBr C,H,0;NJ C,FH,,04N;S, C,H, NSP C,H,,NJP C,H,0,NCl C.H,,O0N,8 C,H,,0,Br8 C,H;; O,NS, C.H,,ONCI1 C,H,,ONJ C.H,0:;NJ C,,H,,0;N,8 E 1264 8) Amid.d. 1-Propyl-4-Isopropylbenzol-ß-Sulfonsäure. Sm. 100—101° (@. 21, 21). — II, 160. 9) Amid d. 2-Propyl-l, 3,5-Trimethylbenzol-4-Sulfonsäure. Sm. 98 bis 99° (B. 28, 2461). Dipropylamid d. Benzolsulfonsäure. Sm. 51° (0. 1898 [2] 888). Chlormethylat d. Pilocarpin. 2-- PtC], (A. 204, 76), — III, 925. 1) Jodmethylat d. Pilocarpin (A. 204, 76). — III, 925. 1) Benzaldehydisoamylthionaminsäure. Sm. 113°. Anilinsalz (A. 274, 196). — III, 6. — IV, 1655. 1) Diäthyl-4-Dimethylamidophenylphosphinoxyd + H,0. : Sm. 65° (A. 260, 25). — IV, 1656. 1) Methyläther d. Methyldiäthyl-4-Oxyphenylphosphoniumchlorid. 2 -+ PtCl, (A. 293, 256). — IV, 1655. 2 1) 4-Methyläther d. Methyldiäthyl-4-Oxyphenylphosphoniumjodid. Sm. 91° (A. 293, 256). — IV, 1655. 1) Chlormethylat d. Anhydroecgoninäthylester. + AuCl, (B. 27, 2453). — III, 871. 1) Jodmethylat d. Anhydroecgoninäthylester. Sm. 177° (B. 27, 2450). — III, 871. 1) Nitrosochlorid d. 44®)-Terpenolacetat. 652, 2292). — III, 481. 2) Chlormethylat d. Mezcalin. 2+PtÜl, 1) Nitrosobromid d. 44®)-Terpenolacetat. — III, 481. 1) Jodmethylat d. Mezcalin. Sm. 174° (B. 31, 1195). 1) Amid d. ?- Aethyl-tert.-Butylbenzol-?-Disulfonsäure. Sm. 228 bis 229° (B. 27, 1613). | 2) Diäthylamid d. 1, 3-Dimethylbenzol-2,4-Disulfonsäure. (B. 23, 3116). — II, 143. ' 1) Diäthylester d. P- Chlor-y-Oximido-ß-Methylpentan-s -Diearbon- säure. Sm. 85--87° (0. 1898 [2] 660). 1) Diäthyl-4-Dimethylamidophenylphosphinsulfid. Sm. 148° (A. 260, 25). — IV, 1656. Sm. 199° (A. 260, 24). — IV, 1654. 1) Chlormethylat d. Hydroecgonidinäthylester. + AuC], (B. 30, 716). 2) Aethylalkoholat d. TLimonennitrosylehlorid. Sm. 114—115° (A. 245, 265). — III, 525. 1) Jodmethylat d. Hydroeegonidinäthylester. 1) Jodmethylat d. N-Methyl-Nor-d-Eegoninäthylester. (B. 26, 1489). — III, 863. 1) Chlormethylat d. 1-Methyltropinsäuredimethylester. (B. 28, 3286). — III, 794. ; 1) Jodmethylat d. i-Methyltropinsäuredimethylester + '/s H,O. Sm. 131—132° (B. 28, 3286). — III, 794. i 2) Jodmethylat d. d-Methyltropinsäuredimethylester. Sm. 121, 21222 (B. 28, 3286). — III, 794. 3 Pr 1 1) Dimethylester d. ö-Sulfondilamidovaleriansäure]. Sm. 81—82° (B. 27, 2015). 1) Diisoamylthetinbromid (J. 1878, 684). — I, 877. 1) 4,4-Diäthylsulfon - 2,2,6- Trimethylhexahydropyridin. (B. 31, 3149). 1) Chloräthylat d. 2-Methyl-3-[a-Oxyäthylj-1-Aethylhexahydro- pyridin. + 5HgCl, + H,0, 2 + PtCl, (4A. 304, 68). | 1) Jodmethylat d. e&- Diisobutylamido -$- Ketopropan. Sm. 288° (B. 29, 871). 2) a d. Aethyleonhydrin (J. 1863, 436). — IV, 35. 1) Jodmethylat d. 1-[88-Dioxyäthyljhexahydropyridindiäthyläther (J. d. Piperidoacetal). Sm. 121° (B. 27, 2017: 28, 1247). — IV, 22. 1) Laurinamidoximschwefligesäure (B. 26, 2845). (A. 168, 30; A. Spl. 1, 224; B. 8, 244). — Sm. 82° (B. 27, 445; 28, (B. 31, 1195). Sm. 81—82° (B. 28, 2292). Sm. 135° Sm. 156° (B. 30, 715). Sm. 190° + Au0l, Sm. 135° I, 308. & | LIBRARY \ 7 J