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CAS No 548-42-5 , Ergoline,8,9-didehydro-6,8-dimethyl- Search by region : Germany

  • Name: Ergoline,8,9-didehydro-6,8-dimethyl-
  • Synonyms: Agroclavine(6CI);8,9-Didehydro-6,8-dimethylergoline;Ergoline,8,9-didehydro-6,8-dimethyl-; Indolo[4,3-fg]quinoline, ergoline deriv.; NSC 93132; (-)-Agroclavine; Agroclavin;
  • CAS Registry Number:
  • Flash Point: 209.3°C
  • Boiling Point: 422.5°Cat760mmHg
  • Density: 1.161g/cm3
  • Refractive index: 1.653
  • Safety Statements: Poison by intraperitoneal route. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.
  • Flash Point: 209.3°C
  • EINECS: 208-947-3
  • Molecular Weight: 238.36
  • InChI: InChI=1/C16H18N2/c1-10-6-13-12-4-3-5-14-16(12)11(8-17-14)7-15(13)18(2)9-10/h3-6,8,13,15,17H,7,9H2,1-2H3
  • Molecular Formula: C16H18 N2
  • Molecular Structure:CAS No:548-42-5 Ergoline,8,9-didehydro-6,8-dimethyl-

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548-42-5 Agroclavine

  • Agroclavine
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References of Ergoline,8,9-didehydro-6,8-dimethyl-
Title: Agroclavine
CAS Registry Number: 548-42-5
CAS Name: 8,9-Didehydro-6,8-dimethylergoline
Molecular Formula: C16H18N2
Molecular Weight: 238.33
Percent Composition: C 80.63%, H 7.61%, N 11.75%
Literature References: A non-peptide ergot alkaloid obtained from cultures of fungi parasitic on Elymus mollis Trin.: Abe et al., JP 49 178336 (1949 to Takeda), C.A. 45, 6352c (1951); Annu. Rep. Takeda Res. Lab. 10, 145, 167, 171 (1951); JP 54 7498 (1954), C.A. 50, 6000b (1956); US 2835675 (1958). Found in fungi parasitic on Pennisetum typhoideum Rich.: Stoll et al., Helv. Chim. Acta 37, 1815 (1954). Structure and stereochemistry: Schreier, ibid. 41, 1984 (1958). Biosynthesis: Floss et al., J. Am. Chem. Soc. 90, 6500 (1968). Synthesis: Plieninger et al., Ann. 743, 95 (1971). Metabolism: Ramstad, Lloydia 31, 327 (1968).
Properties: Rods from ether, dec 198-203°; needles from acetone, dec 205-206°. [a]D20 -155° (c = 0.9 in chloroform); [a]D20 -182° (c = 0.5 in pyridine). uv max: 225, 284, 293 nm (e 4.47, 3.88, 3.81). Freely sol in alc, chloroform, pyridine; sol in benzene, ether; very slightly sol in water.
Optical Rotation: [a]D20 -155° (c = 0.9 in chloroform); [a]D20 -182° (c = 0.5 in pyridine)
Absorption maximum: uv max: 225, 284, 293 nm (e 4.47, 3.88, 3.81)