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Scoparone

产品号 Bio-0192 公司名称 InterBioScreen
CAS号 120-08-1 公司网站 http://www.ibscreen.com
分子式 C11H10O4 电 话 +7 49652 40091
分子量 206.1947 传 真 +7 49652 40092
纯 度 电子邮件 screen@ibscreen.chg.ru
保 存 Chembase数据库ID: 150666

产品价格信息

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产品别名

标题
Scoparone
IUPAC标准名
6,7-dimethoxy-2H-chromen-2-one
IUPAC传统名
6,7-dimethoxy-2H-chromen-2-one
别名
Scoparin
Escoparone

产品登记号

CAS号 120-08-1

产品性质

应用领域 Antifungal activity
生物来源 Found in several citrus oils, in Artemisia scoparia, Zanthoxylum setosum and other plants
生物活性机理 Cytochrome P450 inductor

产品详细信息

参考文献

  • Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 324A; 324C; 326C, (ir)
  • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 2, 1314C; 1318A, (nmr)
  • Head, F.S.H. et al., J.C.S., 1939, 1266, (synth)
  • Bohlmann, F. et al., Chem. Ber., 1957, 90, 1512, (synth)
  • Jain, B.D., Anal. Chim. Acta, 1967, 37, 1358, (detn, Nb, U)
  • Bursey, M.M. et al., Chem. Comm., 1967, 712, (ms)
  • McCabe, P.H. et al., J.C.S.(C), 1967, 145, (Prenyletin)
  • Dean, F.M. et al., Tet. Lett., 1967, 2147, (Prenyletin)
  • Khan, M.A.S. et al., Anal. Chim. Acta, 1968, 43, 153, (pmr)
  • Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhuser Verlag, Basel, 1972, nos. 1325-1327, (occur)
  • Sato, M. et al., Phytochemistry, 1972, 11, 657, (biosynth)
  • Gnther, H. et al., Org. Magn. Reson., 1975, 7, 339, (cmr, deriv)
  • Cussans, N.J. et al., Tetrahedron, 1975, 31, 2719, (cmr)
  • Murray, R.D.H. et al., The Natural Coumarins, J. Wiley, 1982, (occur, rev)
  • Kelkar, S.L. et al., Indian J. Chem., Sect. B, 1984, 23, 458, (synth)
  • Joseph-Nathan, P. et al., J. Het. Chem., 1984, 21, 1141, (pmr, deriv)
  • Abu-Eittah, R.H. et al., Can. J. Chem., 1985, 63, 1173, (uv)
  • Jackson, Y.A. et al., Heterocycles, 1995, 41, 1979, (synth)
  • Dubery, I.A. et al., Phytochemistry, 1999, 50, 983-989, (Scoparone, activity)
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, DRS800