(3aR,4R,5R,6aS)-4-((S,E)-3-Hydroxyoct-1-en-1-yl)-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoate - Names and Identifiers
Name | 2H-Cyclopenta[b]furan-2-one,5-(benzoyloxy)hexahydro-4-[(1E,3S)-3-hydroxy-1-octen-1-yl]-,(3aR,4R,5R,6aS)-
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Synonyms | 2H-Cyclopenta[b]furan-2-one,5-(benzoyloxy)hexahydro-4-[(1E,3... (3AR,4R,5R,6aS)-4-((S,E)-3-Hydroxyoct-1-en-1-yl)-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl ben (3AR,4R,5R,6aS)-4-((S,E)-3-Hydroxyoct-1-en-1-yl)-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoa (3aR,4R,5R,6aS)-4-((S,E)-3-Hydroxyoct-1-en-1-yl)-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoate 2H-Cyclopenta[b]furan-2-one, 5-(benzoyloxy)hexahydro-4-[(1E,3S)-3-hydroxy-1-octenyl]-, (3aR,4R,5R,6aS)- 2H-Cyclopenta[b]furan-2-one,5-(benzoyloxy)hexahydro-4-[(1E,3S)-3-hydroxy-1-octen-1-yl]-,(3aR,4R,5R,6aS)- 2H-Cyclopenta[b]furan-2-one,5-(benzoyloxy)hexahydro-4-[(1E,3S)-3-hydroxy-1-octen-1-yl]-, (3aR,4R,5R,6aS)- 2H-Cyclopenta[b]furan-2-one,5-(benzoyloxy)hexahydro-4-[(1E,3S)-3- hydroxy -1-octen-1-yl]-, (3aR,4R,5R,6aS)-
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CAS | 40834-88-6
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(3aR,4R,5R,6aS)-4-((S,E)-3-Hydroxyoct-1-en-1-yl)-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoate - Physico-chemical Properties
Molecular Formula | C22H28O5
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Molar Mass | 372.45 |
Storage Condition | 2-8°C |
Sensitive | IRRITANT |
MDL | MFCD23115474 |
(3aR,4R,5R,6aS)-4-((S,E)-3-Hydroxyoct-1-en-1-yl)-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl benzoate - Introduction
Name: 2H-Cyclopenta [B] furan-2-one,5-(benzoyloxy)hexahydro-4-[(1E,3S)-3-hydroxy-1-octen-1-yl]-,(3aR,4R,5R,6aS)-
Nature:
-Appearance: This compound is a colorless to slightly yellow solid.
-Molecular formula: C27H38O4
-Molecular weight: 422.595g/mol
-Melting point: about 74-76°C
-Boiling point: about 508.6°C
-Solubility: It is miscible in organic solvents, such as ethanol, dimethyl sulfoxide and dichloromethane.
Use:
The compound has a wide range of uses, including but not limited to the following:
-Drug: It is a biologically active molecule that can be used in drug synthesis or drug research.
-Chemical synthesis: It can be used as an intermediate for the synthesis of organic compounds.
-Insect-borne fungicides: Studies have shown that this compound has a certain bactericidal effect on insects.
Preparation Method:
The process for preparing this compound is complex and involves a multi-step reaction. A common method of preparation is as follows:
First, 6-benzyloxycyclopentene is formed between cyclopentene and benzoyl chloride through a chemical reaction.
Then, under the corresponding conditions, 6-benzyloxycyclopentene and 1-octene are reacted to obtain the corresponding (1E,3S)-3-hydroxy-1-octen-1-yl compound.
Next, the (1E,3S)-3-hydroxy-1-octen-1-yl compound and benzoic acid are reacted to produce an acid cycloaddition product of 5-(benzoyloxy) hexahydro-4-[(1E,3S)-3-hydroxy-1-octen-1-yl] cyclopentene.
Finally, 2H-Cyclopenta [B] furan-2-one,5-(benzoyloxy)hexahydro-4-[(1E,3S)-3-hydroxy-1-octen-1-yl]-,(3aR,4R,5R,6aS)-were synthesized from the acid cycloaddition product by a high-temperature reaction-.
Safety Information:
At present, the safety and toxicity of this compound have not been studied in detail. Therefore, it is necessary to follow laboratory safety regulations when using or handling, and take appropriate personal protective measures, such as wearing gloves, wearing laboratory clothes and using chemical exhaust hood. At the same time, it is recommended to operate under the guidance of professionals in related fields, and to deal with the compound in strict accordance with relevant laws and regulations.
Last Update:2024-04-09 21:01:54