5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester
5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester
CAS: 42542-01-8
Molecular Formula: C18H26O5
5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester - Names and Identifiers
5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester - Physico-chemical Properties
| Molecular Formula | C18H26O5 |
| Molar Mass | 322.4 |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD23135396 |
5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester - Introduction
5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester, also known as 5-heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl] methyl ester. The following is a description of the properties, uses, preparation and safety information of this compound:
Nature:
-Appearance: Liquid
-Molecular formula: C16H24O4
-Molecular weight: 280.36g/mol
-Melting Point: Unknown
-Boiling Point: Unknown
-Density: Unknown
-Solubility: Soluble in polar organic solvents such as alcohols and ethers
Use:
-5-heptenoic acid, 7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl) oxy]-1-cyclopenten-1-yl] methyl ester can be used as an intermediate in organic synthesis.
-It may also be biologically active and has potential for further research.
Preparation Method:
-Preparation of 5-heptenoic acid, 7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl) oxy]-1-cyclopenten-1-yl] The specific preparation method of methyl ester may vary due to research needs.
-Generally, the preparation can be carried out by organic synthesis methods, using corresponding raw materials and reaction conditions.
Safety Information:
The safety of 5-heptenoic acid, 7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl) oxy]-1-cyclopenten-1-yl] methyl ester has not been fully studied and reported.
-Appropriate laboratory practices and personal protective measures must be taken when using and handling the compound.
-It may be irritating and harmful to the skin, eyes and respiratory tract, so it is necessary to use protective gloves, goggles and respiratory protective equipment during operation.
-When used, comply with appropriate chemical waste disposal methods. Please refer to the relevant safety literature and materials for more detailed safety information.
Nature:
-Appearance: Liquid
-Molecular formula: C16H24O4
-Molecular weight: 280.36g/mol
-Melting Point: Unknown
-Boiling Point: Unknown
-Density: Unknown
-Solubility: Soluble in polar organic solvents such as alcohols and ethers
Use:
-5-heptenoic acid, 7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl) oxy]-1-cyclopenten-1-yl] methyl ester can be used as an intermediate in organic synthesis.
-It may also be biologically active and has potential for further research.
Preparation Method:
-Preparation of 5-heptenoic acid, 7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl) oxy]-1-cyclopenten-1-yl] The specific preparation method of methyl ester may vary due to research needs.
-Generally, the preparation can be carried out by organic synthesis methods, using corresponding raw materials and reaction conditions.
Safety Information:
The safety of 5-heptenoic acid, 7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl) oxy]-1-cyclopenten-1-yl] methyl ester has not been fully studied and reported.
-Appropriate laboratory practices and personal protective measures must be taken when using and handling the compound.
-It may be irritating and harmful to the skin, eyes and respiratory tract, so it is necessary to use protective gloves, goggles and respiratory protective equipment during operation.
-When used, comply with appropriate chemical waste disposal methods. Please refer to the relevant safety literature and materials for more detailed safety information.
Last Update：2024-04-10 22:29:15
![5-Heptenoic acid,7-[5-oxo-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1-cyclopenten-1-yl]-,methyl ester](http://res.chembk.com/assets/str/2d/4/42/42542-01-8.png)
Supplier List
View History