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CAS No 92-61-5 , 7-hydroxy-6-methoxychromen-2-one Search by region : Switzerland

  • Name: 7-hydroxy-6-methoxychromen-2-one
  • Synonyms: Murrayetin;Gelseminic acid; Escopoletin; Scopoletine;7-hydroxy-6-methoxychromen-2-one; 7-Hydroxy-6-methoxycoumarin; 6-Methylesculetin; Scopoletol; Chrysatropic acid;
  • CAS Registry Number:
  • Melting Point: 200-207 ºC
  • Flash Point: 172.4ºC
  • Boiling Point: 413.5ºC at 760 mmHg
  • Density: 1.377 g/cm3
  • Refractive index: 1.609
  • Safety Statements: R36/37/38
  • Hazard Symbols: Xi: Irritant;
  • Flash Point: 172.4ºC
  • EINECS: 202-171-9
  • Molecular Weight: 192.16812
  • InchiKey: RODXRVNMMDRFIK-UHFFFAOYSA-N
  • InChI: InChI=1S/C10H8O4/c1-13-9-4-6-2-3-10(12)14-8(6)5-7(9)11/h2-5,11H,1H3
  • Risk Statements: S26;S37/39
  • Molecular Formula: C10H8O4
  • Molecular Structure:CAS No:92-61-5 7-hydroxy-6-methoxychromen-2-one

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92-61-5 S-2000 SCOPOLETIN

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References of 7-hydroxy-6-methoxychromen-2-one
Title: Scopoletin
CAS Registry Number: 92-61-5
CAS Name: 7-Hydroxy-6-methoxy-2H-1-benzopyran-2-one
Synonyms: 7-hydroxy-6-methoxycoumarin; 6-methoxyumbelliferone; b-methylesculetin; chrysatropic acid; gelseminic acid
Molecular Formula: C10H8O4
Molecular Weight: 192.17
Percent Composition: C 62.50%, H 4.20%, O 33.30%
Literature References: The aglucone of scopolin. Occurs in root of Scopolia japonica Maxim., Scopolia carniolica Jacq., Atropa belladonna L., Solanaceae, Convolvulus scammonia L., Convolvulaceae. Isoln: Eykman, Ber. 17 III, 442 (1884). Synthesis: Crosby, J. Org. Chem. 26, 1215 (1961); Desai, Desai, J. Indian Chem. Soc. 40, 456 (1963).
Properties: Needles or prisms from chloroform or acetic acid, mp 204°. uv max: 230, 254, 260, 298, 346 nm (log e 4.11, 3.68, 3.63, 3.68, 4.07), Ballantyne et al., Tetrahedron 27, 871 (1971). Slightly sol in water or cold alcohol; sol in hot alcohol or hot glacial acetic acid; moderately sol in chloroform. Practically insol in benzene. Its alcoholic soln has a blue fluorescence. Reduces Fehling's soln.
Melting point: mp 204°
Absorption maximum: uv max: 230, 254, 260, 298, 346 nm (log e 4.11, 3.68, 3.63, 3.68, 4.07), Ballantyne et al., Tetrahedron 27, 871 (1971)