6(2H)-Benzofuranone, 4-ethoxyhexahydro-3a-hydroxy-, (3aS,4S,7aS)- - Names and Identifiers
Name | 6(2H)-Benzofuranone,4-ethoxyhexahydro-3a-hydroxy-,(3aR,4S,7aR)-rel-(-)-(9CI)
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Synonyms | 5-O-Ethylcleroindicin D 6(2H)-Benzofuranone, 4-ethoxyhexahydro-3a-hydroxy-, (3aS,4S,7aS)- 6(2H)-Benzofuranone,4-ethoxyhexahydro-3a-hydroxy-,(3aR,4S,7aR)-rel-(-)-(9CI)
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CAS | 488138-32-5
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6(2H)-Benzofuranone, 4-ethoxyhexahydro-3a-hydroxy-, (3aS,4S,7aS)- - Physico-chemical Properties
Molecular Formula | C10H16O4
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Molar Mass | 200.23 |
Density | 1.21±0.1 g/cm3(Predicted) |
Boling Point | 337.4±42.0 °C(Predicted) |
pKa | 13.39±0.40(Predicted) |
Storage Condition | 2-8℃ |
6(2H)-Benzofuranone, 4-ethoxyhexahydro-3a-hydroxy-, (3aS,4S,7aS)- - Introduction
6(2H)-Benzofuranone, (3aR,4S,7aR)-rel-(-)-(9CI) is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 6(2H)-Benzofuranone, (3aR,4S,7aR)-rel-(-)-(9CI) is a colorless to light yellow solid.
-Solubility: Soluble in ethanol and dichloromethane.
Use:
- 6(2H)-Benzofuranone, (3aR,4S,7aR)-rel-(-)-(9CI) has antibacterial and anti-inflammatory effects, it can be used in drug research and development.
Method:
- 6(2H)-Benzofuranone, (3aR,4S,7aR)-rel-(-)-(9CI) can be prepared in many ways, it depends on the target synthesis strategy and reaction conditions. One possible preparation method involves carrying out a ring-closing reaction and a functional group change on an appropriate starting compound.
Safety Information:
- 6(2H)-Benzofuranone, (3aR,4S,7aR)-rel-(-)-(9CI) safety, information on toxicity and its effects on the human body may be very limited. When using this compound, standard laboratory safety operating procedures should be followed and evaluated according to the safety data provided by the chemical supplier or relevant literature. In addition, for newly synthesized compounds, a comprehensive toxicology and safety assessment must be carried out to ensure their safety during use.
Last Update:2024-04-09 20:52:54