1,2-Benzenediol, 5-(2-propen-1-yl)-3-[4-(2-propen-1-yl)phenoxy]-
obovatol
CAS: 83864-78-2
Molecular Formula: C18H18O3
1,2-Benzenediol, 5-(2-propen-1-yl)-3-[4-(2-propen-1-yl)phenoxy]- - Names and Identifiers
| Name | obovatol |
| Synonyms | obovatol 5-(2-Propenyl)-3-[4-(2-propenyl)phenoxy]-1,2-benzenediol 1,2-Benzenediol, 5-(2-propen-1-yl)-3-[4-(2-propen-1-yl)phenoxy]- |
| CAS | 83864-78-2 |
1,2-Benzenediol, 5-(2-propen-1-yl)-3-[4-(2-propen-1-yl)phenoxy]- - Physico-chemical Properties
| Molecular Formula | C18H18O3 |
| Molar Mass | 282.33 |
| Density | 1.149±0.06 g/cm3(Predicted) |
| Boling Point | 413.6±45.0 °C(Predicted) |
| pKa | 9.30±0.15(Predicted) |
| Storage Condition | 2-8℃ |
1,2-Benzenediol, 5-(2-propen-1-yl)-3-[4-(2-propen-1-yl)phenoxy]- - Introduction
obovatol is a natural compound extracted from a plant called southeastern maurocypress with the chemical formula C20H16O2.
Regarding the nature of obovatol, it is a yellow crystalline solid with a special woody aroma. Its melting point is 147-150 degrees Celsius, and its solubility is low.
obovatol has many biological activities, with antioxidant and anti-inflammatory effects. It has also been reported to inhibit cell proliferation and anti-tumor activity, so it is widely used in biomedical research.
The method of preparing obovatol is generally by extracting it from the bark and wood of southeastern cedar plants. Specific methods include leaching, separation, purification and other steps.
As for the safety information of obovatol, little is known about its toxicity and safety. Therefore, care should be taken when using obovatol, follow laboratory safety practices and avoid exposure to potentially harmful substances. At the same time, should follow the relevant laws and regulations and ethical guidelines for legitimate research and application.
Regarding the nature of obovatol, it is a yellow crystalline solid with a special woody aroma. Its melting point is 147-150 degrees Celsius, and its solubility is low.
obovatol has many biological activities, with antioxidant and anti-inflammatory effects. It has also been reported to inhibit cell proliferation and anti-tumor activity, so it is widely used in biomedical research.
The method of preparing obovatol is generally by extracting it from the bark and wood of southeastern cedar plants. Specific methods include leaching, separation, purification and other steps.
As for the safety information of obovatol, little is known about its toxicity and safety. Therefore, care should be taken when using obovatol, follow laboratory safety practices and avoid exposure to potentially harmful substances. At the same time, should follow the relevant laws and regulations and ethical guidelines for legitimate research and application.
Last Update：2024-04-09 21:54:55
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CAS: 83864-78-2
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Mobile: 18021002903
QQ: 3008007409
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CAS: 83864-78-2
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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