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Umbelliferone

Catalog No. Bio-0198 Name InterBioScreen
CAS Number 93-35-6 Website http://www.ibscreen.com
M. F. C9H6O3 Telephone +7 49652 40091
M. W. 162.14214 Fax
Purity Email screen@ibscreen.chg.ru
Storage Chembase ID: 67538

SYNONYMS

IUPAC name
7-hydroxy-2H-chromen-2-one
IUPAC Traditional name
7-hydroxy-2H-chromen-2-one
Synonyms
Umbelliferone
Skimmetin
Hydrangin
7-hydroxycoumarin

DATABASE IDS

CAS Number 93-35-6

PROPERTIES

Application(s) Antifungal agent
Application(s) Sunscreen agent
Biological Source Occurs widely in plants including Angelica, Artemisia, Coronilla, Ferula and Ruta spp. Phytoalexin of infected sweet potato

DETAILS

REFERENCES

  • Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 323A; 323C; 325B, (ir)
  • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 2, 1312C; 1313C; 1315C, (nmr)
  • Sethna, S. et al., Org. React. (N.Y.), 1953, 7, 20, (synth)
  • Sen, K. et al., J.O.C., 1959, 24, 316, (synth, uv)
  • Barnes, C.J. et al., Aust. J. Chem., 1964, 17, 975, (ms)
  • das Gupta, A.K. et al., J.C.S.(C), 1969, 29, (synth)
  • Hata, K. et al., Chem. Pharm. Bull., 1971, 19, 640, (isol)
  • Lassak, E.V. et al., Aust. J. Chem., 1972, 25, 2491, (derivs)
  • Karrer, W. et al., Konstitution und Vorkommen der Organischen Pflanzenstoffe, 2nd edn., Birkhuser Verlag, Basel, 1972, nos. 1320; 132; 1321, (occur)
  • Gonzlez, A.G. et al., An. Quim., 1973, 69, 1013, (pmr)
  • Huitnik, G.M. et al., Talanta, 1974, 21, 1193, (detn, Ca, Cu)
  • Gnther, H. et al., Org. Magn. Reson., 1975, 7, 339, (cmr, deriv)
  • Brown, D. et al., Phytochemistry, 1975, 14, 1083, (isol)
  • Cussans, N.J. et al., Tetrahedron, 1975, 31, 2719, (cmr)
  • Holzbecher, Z. et al., Handbook of Organic Reagents in Inorganic Analysis, Horwood, Chichester, 1976, (ind)
  • Murray, R.D.H., Prog. Chem. Org. Nat. Prod., 1978, 35, 200, (rev)
  • Hardt, T.J., Diss. Abstr. Int., B, 1982, 43, 1445, (pharmacol)
  • Ritschel, W.A. et al., Arzneim.-Forsch., 1983, 33, 836, (metab)
  • Joseph-Nathan, P. et al., J. Het. Chem., 1984, 21, 1141, (pmr, deriv)
  • Ueno, K., Acta Cryst. C, 1985, 41, 1786, (cryst struct)
  • Abu-Eittah, R.H. et al., Can. J. Chem., 1985, 63, 1173, (uv)
  • Talapatra, B. et al., Indian J. Chem., Sect. B, 1986, 25, 1122, (synth)
  • Ulubelen, A. et al., J. Nat. Prod., 1986, 49, 692, (Ac)
  • Gray, A.I. et al., Phytochemistry, 1987, 26, 257, (deriv)
  • Ishii, H. et al., Chem. Pharm. Bull., 1991, 39, 3100, (synth, deriv)