64812-88-0 - Names and Identifiers
Name | 5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester,[3R-(Z)]-
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Synonyms | (Z)-Methyl 7-((3R)-5-oxo-3-((tetrahydro-2H-pyran-2-yl)oxy)cyclopent-1-en-1-yl)hept-5-enoate 5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester,[3R-(Z)]- 5-Heptenoic acid, 7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-, Methyl ester, [3R-(Z)]- 5-Heptenoic acid, 7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-, methyl ester, [3R-(Z)]- 5-Heptenoic acid, 7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-, methyl ester, [3R-(Z)]- (9CI)
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CAS | 64812-88-0
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64812-88-0 - Physico-chemical Properties
Molecular Formula | C18H26O5
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Molar Mass | 322.4 |
Density | 1.12±0.1 g/cm3(Predicted) |
Boling Point | 463.3±45.0 °C(Predicted) |
Storage Condition | 2-8°C |
64812-88-0 - Introduction
5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester,[3R-(Z)]-(also known as 5-heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl] is an organic compound, its chemical structure contains two carbon chains, cyclopentene and heptene. The following is a description of the properties, uses, preparation methods and safety information of the compound:
Nature:
-Appearance: colorless liquid
-Molecular formula: C15H24O4
-Molecular weight: 268.35g/mol
-Melting point: No data
-Boiling Point: No data
-Density: No data
-Solubility: No data
-Stability: Stable under normal temperature and pressure, but avoid high temperature and strong oxidants.
Use:
- 5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester,[3R-(Z)]-is a chemical intermediate that can be used to synthesize other organic compounds.
-May be used in the field of medicine, such as the synthesis of certain drug precursors.
Preparation Method:
5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester,[3R-(Z)]-can be prepared by chemical synthesis, and the specific steps may include the following steps:
1. Prepare the starting materials: heptenoic acid, pyran and methanol.
2. first, heptenoic acid is partially oxidized by acid catalysis to form heptanone.
3. A cyclopentanol compound is generated by a ring-closing reaction with pyran.
4. finally, the cyclopentanol compound is esterified with methanol to obtain the target product 5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester,[3R-(Z)]-.
Safety Information:
-Since no detailed safety data is available, the specific safety information for this compound is limited to evaluation.
-Follow safe operating procedures for organic compounds, including wearing appropriate protective equipment and avoiding contact with skin and eyes.
-During operation, it should be used in a well-ventilated environment and protective measures should be taken to avoid inhalation or intake.
-If accidental exposure or inhalation occurs, seek medical help immediately and provide detailed information about the compound to the doctor.
Last Update:2024-04-09 21:04:16