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Altholactone
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商品详情
客户评价
| 密度 | 1.3±0.1 g/cm3 |
|---|---|
| 沸点 | 490.4±45.0 °C at 760 mmHg |
| 分子式 | C13H12O4 |
| 分子量 | 232.232 |
| 闪点 | 196.1±22.2 °C |
| 精确质量 | 232.073563 |
| PSA | 55.76000 |
| LogP | 1.00 |
| 蒸汽压 | 0.0±1.3 mmHg at 25°C |
| 折射率 | 1.598 |
| 储存条件 | ?20°C |
| 符号 |
GHS06 |
|---|---|
| 信号词 |
Danger |
| 危害声明 |
H301 |
| 警示性声明 |
P301 + P310 |
| 危害码 (欧洲) |
T |
| 风险声明 (欧洲) |
25 |
| 安全声明 (欧洲) |
45 |
| 危险品运输编码 | UN 2811 6.1 / PGIII |
|
Stereoselective total synthesis of bioactive styryllactones (+)-goniofufurone, (+)7-epi-goniofufurone, (+)-goniopypyrone, (+)-goniotriol, (+)-altholactone, and (-)-etharvensin. J. Org. Chem. 73(1) , 2-11, (2008)
Stereoselective total synthesis of biologically active styryllactones 7-epi-goniofufurone, goniofufurone, goniopypyrone, goniotriol, altholactone, and etharvensin was achieved in high overall yields f…
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The cytotoxicity of naturally occurring styryl lactones. Phytomedicine 13(3) , 181-6, (2006)
We extracted and isolated three natural styryl lactones from Goniothalamus griffithii Hook f. Thoms and investigated their cytotoxicity on a panel of three hepatocyte cell lines, HepG2, drug resistant…
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Asymmetric synthesis of (+)-altholactone: a styryllactone isolated from various Goniothalamus species. Chemistry 14(9) , 2842-9, (2008)
The asymmetric total synthesis of (+)-altholactone (1), a member of the styryllactone family of natural products displaying cytotoxic and antitumor activities, is described. Key steps include a RAMP-h…
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2-phenyl-3-hydroxy-6,7-dihydro-furano-pyrone |
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(2R,3R,3aS,7aS)-3-Hydroxy-2-phenyl-2,3,3a,7a-tetrahydro-5H-furo[3,2-b]pyran-5-one |
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goniothalenol |
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