Home > Name List By other > (6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de, g]quinoline-11-ol

CAS No 475-67-2 , (6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,
g]quinoline-11-ol

  • Name: (6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,
    g]quinoline-11-ol
  • Synonyms: L-(+)-Isocorydine; Artabotrin; Luteanin; Isocorydine (+); Luteanine; d-Isocorydine;(6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,
    g]quinoline-11-ol; Uzokoridin;Artabotrine;
  • CAS Registry Number:
  • Melting Point: 216-220 °C(lit.)
  • Flash Point: 259.9°C
  • Boiling Point: 506.1°Cat760mmHg
  • Density: 1.222g/cm3
  • Refractive index: 1.603
  • Safety Statements:
    WGK Germany 3
    RTECS CE1057950
  • Flash Point: 259.9°C
  • Molecular Weight: 341.40092
  • InchiKey: QELDJEKNFOQJOY-ZDUSSCGKSA-N
  • InChI: InChI=1S/C20H23NO4/c1-21-8-7-12-10-15(24-3)20(25-4)18-16(12)13(21)9-11-
    5-6-14(23-2)19(22)17(11)18/h5-6,10,13,22H,7-9H2,1-4H3/t13-/m0/s1
  • Molecular Formula: C20H23NO4
  • Molecular Structure:CAS No:475-67-2 (6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,<br />g]quinoline-11-ol

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475-67-2 Isocorydine

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475-67-2 ISOCORYDINE HYDROCHLORIDE FROM STEPHANIA BRACHYANDRA

  • ISOCORYDINE HYDROCHLORIDE FROM STEPHANIA BRACHYANDRA
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475-67-2 (+)-ISOCORYDINE

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References of (6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,
g]quinoline-11-ol
Title: Isocorydine
CAS Registry Number: 475-67-2
CAS Name: (6aS)-5,6,6a,7-Tetrahydro-1,2,10-trimethoxy-6-methyl-4H-dibenzo[de,g]quinolin-11-ol
Synonyms: 1,2,10-trimethoxy-6aa-aporphin-11-ol; 11-hydroxy-1,2,10-trimethoxyaporphine; artabotrine; luteanine
Molecular Formula: C20H23NO4
Molecular Weight: 341.40
Percent Composition: C 70.36%, H 6.79%, N 4.10%, O 18.75%
Literature References: From tubers of Corydalis cava (L.) Schweigg. & Korte (C. tuberosa DC., Fumariaceae); Artabotrys suaveolens Blume, Anonaceae; Papaver oreophilum Rupr.; Phoebe clemensii Allen (Lauraceae) and others. Isoln: Gadamer, Arch. Pharm. 249, 669 (1911); Johns, Lamberton, Aust. J. Chem. 20, 1277 (1967); Pfeifer, Mann, Pharmazie 23, 82 (1968). Structure: Sp?th, Berger, Ber. 64, 2038 (1931); Gulland et al., J. Chem. Soc. 1931, 2885; Barger, Sargent, ibid. 1939, 991. Identity with artabotrine: Schlittler, Huber, Helv. Chim. Acta 35, 111 (1952); with luteanine: Manske, Can. J. Res. 21B, 13 (1943). Total synthesis: Kametani et al., Tetrahedron 27, 5367 (1971). Pharmacology: Berezhinskaya et al., Farmakol. Toksikol. (Moscow) 31, 44 (1968), C.A. 68, 94521z (1968).
Properties: Plates from ethanol or acetone, mp 185°. [a]D20 +195° (chloroform). Sol in ether, chloroform, alcohol, acetone, alkali hydroxide. Practically insol in water, alkali carbonates.
Melting point: mp 185°
Optical Rotation: [a]D20 +195° (chloroform)