Furan, 2,5-diethyl-
2,5-diethylfuran
CAS: 10504-06-0
Molecular Formula: C8H12O
Furan, 2,5-diethyl- - Names and Identifiers
| Name | 2,5-diethylfuran |
| Synonyms | 2,5-diethylfuran Furan, 2,5-diethyl- |
| CAS | 10504-06-0 |
Furan, 2,5-diethyl- - Physico-chemical Properties
| Molecular Formula | C8H12O |
| Molar Mass | 124.18 |
Furan, 2,5-diethyl- - Introduction
2,5-Diethylfuran (2,5-diethylfuran) is an organic compound with the chemical formula C9H14O. Its nature is as follows:
1. appearance: 2,5-diethyl furan is a colorless liquid, similar to the pungent odor.
2. Density: Its density is 0.804 g/mL.
3. Boiling point and melting point: 2,5-diethylfuran has a boiling point of about 125-127°C and a melting point of about -57°C.
4. Solubility: The compound is easily soluble in a variety of solvents, such as alcohols, ethers and aromatic hydrocarbons.
5. Stability: 2,5-diethyl furan is stable, but may cause dangerous combustion reactions when encountering oxidants.
The compound has a wide range of uses, including but not limited to the following:
1. Organic synthesis: 2,5-diethylfuran can be used as a solvent and intermediate in organic synthesis, and can be used to synthesize biologically active compounds and drugs.
2. Fragrances and flavors: Due to its special smell, 2,5-diethylfuran can also be used to prepare perfumes, fragrances and flavors.
3. Coating and solvent: The compound can also be used as a component of coating and solvent.
The preparation method of 2,5-diethylfuran can be carried out by the following steps:
1. First, ethyl chloride and sodium hydroxide are reacted to generate ethanol.
2. Ethanol reacts with cuprous chloride to produce Diethylcuprate.
3. The Diethylcuprate is then reacted with chloroacetic acid to produce Diethylfuran-2,5-dicarboxylate.
4. Finally, through acid catalysis or hydrolysis reaction, Diethylfuran-2,5-dicarboxylate is converted into 2,5-diethylfuran.
Note the following safety information when using 2,5-diethyl furan:
1. The compound has a pungent odor and should be kept away from fire and high temperature to prevent burning and explosion.
2. Avoid contact with strong oxidants to avoid dangerous reactions.
3. Wear appropriate personal protective equipment such as gloves and safety glasses during use.
4. Pay attention to comply with the relevant safety regulations during use and storage to ensure personal safety and environmental protection.
1. appearance: 2,5-diethyl furan is a colorless liquid, similar to the pungent odor.
2. Density: Its density is 0.804 g/mL.
3. Boiling point and melting point: 2,5-diethylfuran has a boiling point of about 125-127°C and a melting point of about -57°C.
4. Solubility: The compound is easily soluble in a variety of solvents, such as alcohols, ethers and aromatic hydrocarbons.
5. Stability: 2,5-diethyl furan is stable, but may cause dangerous combustion reactions when encountering oxidants.
The compound has a wide range of uses, including but not limited to the following:
1. Organic synthesis: 2,5-diethylfuran can be used as a solvent and intermediate in organic synthesis, and can be used to synthesize biologically active compounds and drugs.
2. Fragrances and flavors: Due to its special smell, 2,5-diethylfuran can also be used to prepare perfumes, fragrances and flavors.
3. Coating and solvent: The compound can also be used as a component of coating and solvent.
The preparation method of 2,5-diethylfuran can be carried out by the following steps:
1. First, ethyl chloride and sodium hydroxide are reacted to generate ethanol.
2. Ethanol reacts with cuprous chloride to produce Diethylcuprate.
3. The Diethylcuprate is then reacted with chloroacetic acid to produce Diethylfuran-2,5-dicarboxylate.
4. Finally, through acid catalysis or hydrolysis reaction, Diethylfuran-2,5-dicarboxylate is converted into 2,5-diethylfuran.
Note the following safety information when using 2,5-diethyl furan:
1. The compound has a pungent odor and should be kept away from fire and high temperature to prevent burning and explosion.
2. Avoid contact with strong oxidants to avoid dangerous reactions.
3. Wear appropriate personal protective equipment such as gloves and safety glasses during use.
4. Pay attention to comply with the relevant safety regulations during use and storage to ensure personal safety and environmental protection.
Last Update：2024-04-10 22:43:14
