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Gibberellic acid

Catalog No. Bio-0832 Name InterBioScreen
CAS Number 77-06-5 Website http://www.ibscreen.com
M. F. C19H22O6 Telephone +7 49652 40091
M. W. 346.37438 Fax
Purity Email screen@ibscreen.chg.ru
Storage Chembase ID: 119594

SYNONYMS

IUPAC name
(1R,2R,5S,8S,9S,10R,11R,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-13-ene-9-carboxylic acid
IUPAC Traditional name
(1R,2R,5S,8S,9S,10R,11R,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-13-ene-9-carboxylic acid
Synonyms
Gibrofit
Gibberellin A3
Gibrescol
GA3
Berelex
Activol

DATABASE IDS

CAS Number 77-06-5

PROPERTIES

Application(s) Plant growth regulator
Application(s) Used in malting of barley
Application(s) Used as an experimental research mutagen
Biological Source Produced by Gibberella fujikuroi and present in higher plants
Mechanism of Action Plant growth factor.
Mechanism of Action Stimulates the cells of germinating seeds to produce mRNA molecules that code for hydrolytic enzymes

DETAILS

REFERENCES

  • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 1, 1145B, (nmr)
  • Aldrich Library of FT-IR Spectra, 1st edn., 1985, 1, 703A, (ir)
  • Cross, B.E. et al., Chem. Comm., 1965, 535, (biosynth)
  • McCapra, F. et al., J.C.S.(C), 1966, 1577, (cryst struct)
  • Schreiber, K. et al., Phytochemistry, 1966, 5, 1221, (isol)
  • Verbiscar, A.J. et al., Phytochemistry, 1967, 7, 807, (biosynth)
  • Yamaguchi, I. et al., Agric. Biol. Chem., 1970, 34, 1439, (deriv)
  • Yokota, T. et al., Agric. Biol. Chem., 1971, 35, 583, (isol)
  • Dawson, R.M. et al., Phytochemistry, 1975, 14, 2593, (biosynth)
  • Hook, J.M. et al., J.A.C.S., 1980, 102, 6628, (synth)
  • Corey, E.J. et al., J.A.C.S., 1982, 104, 6129, (synth)
  • Kutschabsky, L. et al., J.C.S. Perkin 1, 1983, 1653, (cryst struct)
  • Schwartz, E. et al., Pharmazie, 1983, 38, 716, (pharmacol)
  • Al-Ekabi, H.K. et al., Can. J. Chem., 1984, 62, 1996, (ms)
  • Hook, J.N. et al., J.O.C., 1984, 49, 3250, (synth)
  • Lewer, P. et al., Phytochemistry, 1984, 23, 2803, (biosynth)
  • Danheiser, R.L., Strategies Tactics Org. Synth., 1984, 21; CA, 102, 6856, (book)
  • Synform, 1984, 2, 197, (rev)
  • Hossain, M.B. et al., Acta Cryst. C, 1988, 44, 1022, (cryst struct)
  • Pesticide Manual, 9th edn., 1991, No. 6910
  • Bhaskar, K.V. et al., Tet. Lett., 1991, 32, 6203, (GA85, GA86)
  • Agrochemicals Handbook, 3rd edn., Royal Society of Chemistry, 1992, A797
  • Sheng, C. et al., Biosci., Biotechnol., Biochem., 1992, 56, 564, (isol, GA85)
  • Blake, P.S. et al., Phytochemistry, 1993, 32, 781, (GA87)
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, GEM000