
CAS Name: (3S-trans)-6-Propyl-3-piperidinol
Additional Names: 5-hydroxy-2-propylpiperidine; 5-hydroxyconiine
Percent Composition: C 67.08%, H 11.96%, N 9.78%, O 11.17%
Literature References: In Conium maculatum L., Umbelliferae (hemlock). Extraction procedure: Ladenburg et al., Ber. 24, 1671 (1891); Braun, Ber. 38, 3108 (1905); Löffler, Ber. 42, 116 (1909). Structure: E. Späth et al., Ber. 66, 591 (1933). Stereochemistry: R. K. Hill, J. Am. Chem. Soc. 80, 1611 (1958); K. Tadano et al., J. Carbohydr. Chem. 4, 129 (1985).
CAS Name: 5,8,13,13a-Tetrahydro-2,9,10-trimethoxy-6H-dibenzo[a,g]quinolizin-3-ol
Additional Names: 2,9,10-trimethoxyberbin-3-ol; 3-hydroxy-2,9,10-trimethoxyberbine; tetrahydrojatrorrhizine
P...
Literature References: In Corydalis cava (L.) Schweigg Körte (C. tuberosa D.C.) and other varieties of Corydalis, Fumariaceae. Synthesis of dl-corypalmine: Govindachari et al., Ber. 92, 1654 (1959).
CAS Name: (6aS)-5,6,6a,7-Tetrahydro-2,10-dimethoxy-6-methyl-4H-dibenzo[de,g]quinoline-1,11-diol
Additional Names: 2,10-dimethoxy-6aa-aporphine-1,11-diol; 1,11-dihydroxy-2,10-dimethoxyaporphine<...
Literature References: In Corydalis cava (L.) Schweigg Körte (C. tuberosa DC), in Dicentra formosa (Andr.) Walp., Fumariaceae. Isoln: Späth, Berger, Ber. 64, 2038 (1931); Manske, Can. J. Res. 10, 521 (1934). Synthesis of (±)-form: Tomita, Kikkawa, JP 58 6466 (1958 to Shionogi), C.A. 54, 1584i (1960); T. Kametani, M. Ihara, J. Chem. Soc. Perkin Trans. 1 1980, 629. Biosynthesis studies: Blaschke, Biochem. Physiol. Alkaloide, Int. Symp., 4th, K. Mothes, Ed. (Akad.-Verlag, Berlin, 1972) pp 283-286. Biomimetric total synthesis: T. Kametani et al., Heterocycles 5, 175 (1976).
CAS Name: (14R)-4,6,7,14-Tetrahydro-5,14-dimethylbis[1,3]benzodioxolo[4,5-c:5',6'-g]azecin-13(5H)-one
Additional Names: 7,13-dimethyl-2,3:9,10-bis(methylenedioxy)-7,13a-secoberbin-13a-one
Pe...
Literature References: In Corydalis cava (L.) Schweigg Korte (C. tuberosa DC.), Fumariaceae: Gadamer et al., Arch. Pharm. 240, 81 (1902). Structure: von Bruchhausen, ibid. 263, 570 (1925). Corycavamine and corycavine originally depicted as the keto and enol tautomers, resp.
CAS Name: 5,8,13,13a-Tetrahydro-2,9,10-trimethoxy-13-methyl-6H-dibenzo[a,g]quinolizin-3-ol
Additional Names: 2,9,10-trimethoxy-13-methyl-13a-berbin-3-ol; 3-hydroxy-13-methyl-2,9,10-trimethoxybe...
Literature References: In Corydalis cava (L.) Schweigg Korte (C. tuberosa DC.); Fumariaceae: Freund, Josephi, Ann. 277, 1 (1893); in C. platycarpa Makino, Fumariaceae: Manske, Can. J. Res. 21B, 13 (1943). Structure: Späth, Dobrowsky, Ber. 58, 1274 (1925).
CAS Name: 2,2'-(2,6-Piperidinediyl)bis[1-phenylethanone]
Additional Names: isolobelanine
Percent Composition: C 78.47%, H 7.21%, N 4.36%, O 9.96%
Literature References: In herb of Lobelia inflata L., Lobeliaceae. Isoln from crude lobelanidine nitrate: Wieland et al., Ann. 473, 118 (1929). Synthesis: Schöpf, Lehmann, ibid. 518, 1 (1935). Cis- and trans-isomers: Ebnöther, Helv. Chim. Acta 41, 386 (1958).
CAS Name: 6-(b-D-Glucopyranosyloxy)-7-hydroxy-2H-1-benzopyran-2-one
Additional Names: 6,7-dihydroxycoumarin 6-glucoside; esculoside; bicolorin; enallachrome; polychrome
Trademarks: Escosyl
CAS Name: N-Methyl-2,5-dihydropyrrole
Percent Composition: C 72.24%, H 10.91%, N 16.85%
Literature References: In leaves of Nicotiana tabacum L. and Atropa belladonna L. By reducing N-methylpyrrole with zinc granules in dil acetic or hydrochloric acid.
CAS Name: (9S)-6,7,8,9-Tetrahydro-4-methoxy-8,9-dimethyl-1,3-dioxolo[4,5-h]isoquinoline
Additional Names: N-methylanhalonine
Percent Composition: C 66.36%, H 7.28%, N 5.95%, O 20.40%
Literature References: In Lophophora williamsii (Lemaire) Coult., Cactaceae. Extraction procedure: Kauder, Arch. Pharm. 237, 191 (1899). Structure: Späth, Gangl, Monatsh. Chem. 44, 104, 106 (1923). Synthesis: Späth, Kesztler, Ber. 68, 1667 (1935).
CAS Name: (6aS)-5,6,6a,7-Tetrahydro-2-methoxy-6-methyl-4H-benzo[de][1,3]benzodioxolo[5,6-g]quinolin-1-ol
Additional Names: 2-methoxy-9,10-(methylenedioxy)-6aa-aporphin-1-ol; 1-hydroxy-2-methoxy...
Literature References: In Nandina domestica Thunb., Berberidaceae. Isoln: Kitasato, Shishido, Ann. 527, 176 (1937). Syntheses: Govindachari et al., Indian J. Chem. 7, 841 (1969); Kessar et al., ibid. 8, 468 (1970); Kametani et al., J. Chem. Soc. C 1971, 2446, 2712; eidem, Chem. Pharm. Bull. 21, 766 (1973); Horii et al., ibid. 22, 583 (1974); Hoshino et al., ibid. 23, 2048 (1975).
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