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CAS No 548-43-6 , Ergoline-8-methanol,8,9-didehydro-6-methyl-

  • Name: Ergoline-8-methanol,8,9-didehydro-6-methyl-
  • Synonyms: Elymoclavine(6CI); Elymoclavin; NSC 109431; D-8,9-Didehydro-6-methylergoline-8-methanol;Ergoline-8-methanol,8,9-didehydro-6-methyl-;
  • CAS Registry Number:
  • Flash Point: 236.8°C
  • Boiling Point: 468°Cat760mmHg
  • Density: 1.247g/cm3
  • Refractive index: 1.676
  • Safety Statements: A poison by intraperitoneal and intravenous routes. Experimental teratogenic and reproductive effects. When heated to decomposition it emits acrid smoke and fumes. See also N,N-DIETHYLLYSERGAMIDE (LSD).
  • Flash Point: 236.8°C
  • EINECS: 208-948-9
  • Molecular Weight: 254.36
  • InChI: InChI=1/C16H18N2O/c1-18-8-10(9-19)5-13-12-3-2-4-14-16(12)11(7-17-14)6-15(13)18/h2-5,7,13,15,17,19H,6,8-9H2,1H3/t13-,15-/m1/s1
  • Molecular Formula: C16H18 N2 O
  • Molecular Structure:CAS No:548-43-6 Ergoline-8-methanol,8,9-didehydro-6-methyl-

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References of Ergoline-8-methanol,8,9-didehydro-6-methyl-
Title: Elymoclavine
CAS Registry Number: 548-43-6
CAS Name: 8,9-Didehydro-6-methylergoline-8-methanol
Molecular Formula: C16H18N2O
Molecular Weight: 254.33
Percent Composition: C 75.56%, H 7.13%, N 11.01%, O 6.29%
Literature References: An ergot alkaloid obtained from cultures of fungi parasitic on Elymus mollis Trin.: Abe et al., US 2835675 (1958). Found in fungi parasitic on Pennisetum typhoideum Rich.: Stoll et al., Helv. Chim. Acta 37, 1815 (1954). Structure and stereochemistry: Schreier, Helv. Chim. Acta 41, 1984 (1958). Biosyntheses utilizing Claviceps cultures: Naidoo et al., Chem. Commun. 1970, 472; Ogunlana et al., ibid. 775; Seiler et al., ibid. 1394; Cavender, Anderson, Biochim. Biophys. Acta 208, 345 (1970).
Properties: Monoclinic prisms from methanol, 248-252° (dec). [a]D20 -59° (c = 0.1 in ethanol) (Abe); [a]D20 -152° (c = 0.9 in pyridine) (Stoll). uv max: 227, 283, 293 nm (log e 4.31, 3.84, 3.76). Fairly sol in water with alkaline reaction. Sol in pyridine; very slightly sol in organic solvents.
Optical Rotation: [a]D20 -59° (c = 0.1 in ethanol) (Abe); [a]D20 -152° (c = 0.9 in pyridine) (Stoll)
Absorption maximum: uv max: 227, 283, 293 nm (log e 4.31, 3.84, 3.76)