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COMMON NAME | : | |
SYMBOL | : | |
FORMULA | : | C6H8O2 MOL.WT (average) : 112.127 |
BIOLOGICAL ACTIVITY |
PHYSICAL AND CHEMICAL PROPERTIES |
MELTING POINT | : | |
BOILING POINT | : | Z-form Bp0.35 60![]() |
REFRACTIVE INDEX | : | |
OPTICAL ROTATION | : | |
DENSITY | : | |
SOLUBILITY | : |
SPECTRAL DATA |
UV SPECTRA | : | |
IR SPECTRA | : | u (CHCl3) 1740, 1700 cm-1(Ref. 0014) |
NMR SPECTRA | : | 1H NMR(CDCl3): d 2.70(m, 4H), 6.15(ddt, 1H), 6.87(dt, 1H), 9.57(d, 1H), 9.83(s, 1H)(Ref. 0014) |
MASS SPECTRA | : | m/e 113(M++1), 95, 85(Ref. 0014) |
OTHER SPECTRA | : | |
CHROMATOGRAM DATA |
SOURCE |
CHEMICAL SYNTHESIS |
METABOLISM |
GENETIC INFORMATION |
NOTE |
REFERENCES |
AUTHOR | : | Hudlicky,T., Luna,H., Barbieri,G., and Kwart,L.D. |
TITLE | : | Enantioselective Synthesis through Microbial Oxidation of Arenes. 1. Efficient Preparation of Terpen and Prostanoid Synthons |
JOURNAL | : | J. Am. Chem. Soc. |
VOL | : | 110 PAGE : 4735 -4741 (1988) |
AUTHOR | : | Dictionary of Organic Compounds Sixth Edition, pp3523 (1996), Champan and Hall, London |
TITLE | : | |
JOURNAL | : | |
VOL | : | PAGE : - () |