|
| COMMON NAME | : | 13-cis-retinal |
| SYMBOL | : | |
| FORMULA | : | C20H28O MOL.WT (average) : 284.436 |
| BIOLOGICAL ACTIVITY |
| PHYSICAL AND CHEMICAL PROPERTIES |
| MELTING POINT | : | 77 C(Ref. 0013) |
| BOILING POINT | : | |
| REFRACTIVE INDEX | : | |
| OPTICAL ROTATION | : | |
| DENSITY | : | |
| SOLUBILITY | : | |
| SPECTRAL DATA |
| UV SPECTRA | : | lmax=375,257nm (E:1250,336 respecticely in ethanol)(Ref. 0013) |
| IR SPECTRA | : | |
| NMR SPECTRA | : | 1H-NMR(d,CDCl3,220MHz):1.04(6H,1-Me),~1.47(2H,J= n.o,2-CH2),~1.63(2H,J=n.o,3-CH2),1.73(3H,5-Me),~2.0(2H,J=n.o,4-Me),2.03(3H,9-Me),2.15(3H,13-Me),5.85(1H,J=8.0Hz,14-H),6.18(1H,J=~16.0Hz,8-H),6.24(1H,J=11.0Hz,10-H),6.36(1H,J=~16.0Hz,7-H),7.04(1H,J=11.0,15.0Hz,11-H),7.30 (1H,J=15.0Hz,12-H),10.21(1H,J=8.0Hz,CHO)(Ref. 0003) 13C-NMR(d,CDCl3,22.63MHz):13.0,19.3,21.1,21.7,29.0,29.0,33.2,34.3,39.7,126.5,127.7,129.4,129.6,130.3,133.4,137.0,137.6,141.3,154.2,174.0(CO)(Ref. 0004) |
| MASS SPECTRA | : | |
| OTHER SPECTRA | : | |
| CHROMATOGRAM DATA |
| SOURCE |
| CHEMICAL SYNTHESIS |
| METABOLISM |
| GENETIC INFORMATION |
| NOTE |
| REFERENCES |
| AUTHOR | : | Schwieter, U., Englert, G., Rigassi, N., and Vetter, W. |
| TITLE | : | Physical organic methods in carotenoid research PubMed ID:5377333 |
| JOURNAL | : | Pure Appl Chem. |
| VOL | : | 20 PAGE : 365-420 (1969) |
| AUTHOR | : | Englert, G. |
| TITLE | : | A 13C-NMR. Study of cis-trans isomeric vitamins A, carotenoids and related compounds PubMed ID:1194053 |
| JOURNAL | : | Helv Chim Acta. |
| VOL | : | 58 PAGE : 2367-2390 (1975) |
| AUTHOR | : | Tsukita kiyoshi, Yoshizawa Tohru, Matsumoto Hiroyuki(1975) Vitamin to Hokouso (eds Nihon Seikagakukai) Chapter.14 Vitamin A pp.549 Tokyo Kagaku Dojin |
| TITLE | : | |
| JOURNAL | : | |
| VOL | : | PAGE : - () |
| AUTHOR | : | Seikagaku Hand Book (eds. Nihon Seikagakukai) pp.1274-1277. Tokyo Kagaku Dojin |
| TITLE | : | |
| JOURNAL | : | |
| VOL | : | PAGE : - () |