373-45-5
2-[2-(2-Fluoroethoxy)ethoxy]ethanol
CAS: 373-45-5
Molecular Formula: C6H13FO3
373-45-5 - Names and Identifiers
| Name | 2-[2-(2-Fluoroethoxy)ethoxy]ethanol |
| Synonyms | 2-[2-(2-Fluoroethoxy)ethoxy]ethanol 2-(2-(2-Fluoroethoxy)ethoxy)ethan-1-ol |
| CAS | 373-45-5 |
373-45-5 - Physico-chemical Properties
| Molecular Formula | C6H13FO3 |
| Molar Mass | 152.16 |
373-45-5 - Upstream Downstream Industry
373-45-5 - Introduction
2-[2-(2-Fluoroethoxy)ethoxy]ethanol is an organic compound with the chemical formula C6H13FO3 and a molecular weight of 152.16g/mol. It is a colorless liquid with a sweet taste at room temperature. The following is a description of the properties, uses, preparation methods and safety information of the compound:
Nature:
-Appearance: colorless liquid
-Solubility: Soluble in water and organic solvents
-Melting point:-89 ° C
-Boiling point: 228-229 ° C
-Density: 1.041 g/mL
-Refractive Index: 1.422
Use:
- 2-[2-(2-Fluoroethoxy)ethoxy]ethanol has certain solvent properties and is often used as a solvent or medium for dissolving other organic compounds.
-It can also be used in organic synthesis reactions as a reaction solvent or additive.
Method:
The preparation of -2-[2-(2-Fluoroethoxy)ethoxy]ethanol can usually be carried out by the following steps:
1. Add 2-fluoroethanol into anhydrous hydrofluoric acid and react at low temperature to generate 2-fluoroacetic acid.
2. 2-fluoroacetic acid and ethylene glycol are reacted under appropriate conditions to generate 2-[2-(2-Fluoroethoxy)ethoxy]ethanol.
Safety Information:
- 2-[2-(2-Fluoroethoxy)ethoxy]ethanol is irritating to the skin and eyes, and care should be taken to avoid contact with the skin and eyes during use.
-When using this compound, wear protective gloves and safety glasses, and make sure to operate in a well-ventilated place.
-When storing and handling the compound, follow safe operating practices and keep away from fire and heat.
-Seek immediate medical attention if the compound is accidentally ingested or inhaled.
Nature:
-Appearance: colorless liquid
-Solubility: Soluble in water and organic solvents
-Melting point:-89 ° C
-Boiling point: 228-229 ° C
-Density: 1.041 g/mL
-Refractive Index: 1.422
Use:
- 2-[2-(2-Fluoroethoxy)ethoxy]ethanol has certain solvent properties and is often used as a solvent or medium for dissolving other organic compounds.
-It can also be used in organic synthesis reactions as a reaction solvent or additive.
Method:
The preparation of -2-[2-(2-Fluoroethoxy)ethoxy]ethanol can usually be carried out by the following steps:
1. Add 2-fluoroethanol into anhydrous hydrofluoric acid and react at low temperature to generate 2-fluoroacetic acid.
2. 2-fluoroacetic acid and ethylene glycol are reacted under appropriate conditions to generate 2-[2-(2-Fluoroethoxy)ethoxy]ethanol.
Safety Information:
- 2-[2-(2-Fluoroethoxy)ethoxy]ethanol is irritating to the skin and eyes, and care should be taken to avoid contact with the skin and eyes during use.
-When using this compound, wear protective gloves and safety glasses, and make sure to operate in a well-ventilated place.
-When storing and handling the compound, follow safe operating practices and keep away from fire and heat.
-Seek immediate medical attention if the compound is accidentally ingested or inhaled.
Last Update：2024-04-10 22:29:15
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373-45-5
2,2'-BIBENZOTHIAZOLE
Methyl2-(2-((3-chloro-5-(trifluoromethyl)-2-pyridinyl)sulfanyl)acetyl)-6-oxohexahydro-4-pyridazinecarboxylate
(Fluorosulfonyl)(trifluoromethanesulfonyl)imide
(2R,5S)-5-(4-Amino-5-fluoro-2-oxo-1(2H)-pyrimidinyl)-1,3-oxathiolane-2-carboxylic acid, (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester
DL-2,4,5-Trifluoro-Phe-OH
2-bromo-3-methyl-N-(2,4,6-trimethylphenyl)butanamide
Ethanone, 1,1'-[2,4-bis(4-methoxyphenyl)-1,3-cyclobutanediyl]bis[2-diazo-, (1α,2α,3β,4β)- (9CI)
5-[(5-bromo-2-furyl)methylene]-2-[(4-bromophenyl)imino]-1,3-thiazolidin-4-one
2,4-Imidazolidinedione,5-[(methylthio)methyl]-
2,2'-BIBENZOTHIAZOLE
Methyl2-(2-((3-chloro-5-(trifluoromethyl)-2-pyridinyl)sulfanyl)acetyl)-6-oxohexahydro-4-pyridazinecarboxylate
(Fluorosulfonyl)(trifluoromethanesulfonyl)imide
(2R,5S)-5-(4-Amino-5-fluoro-2-oxo-1(2H)-pyrimidinyl)-1,3-oxathiolane-2-carboxylic acid, (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester
DL-2,4,5-Trifluoro-Phe-OH
2-bromo-3-methyl-N-(2,4,6-trimethylphenyl)butanamide
Ethanone, 1,1'-[2,4-bis(4-methoxyphenyl)-1,3-cyclobutanediyl]bis[2-diazo-, (1α,2α,3β,4β)- (9CI)
5-[(5-bromo-2-furyl)methylene]-2-[(4-bromophenyl)imino]-1,3-thiazolidin-4-one
2,4-Imidazolidinedione,5-[(methylthio)methyl]-
Raw Materials for 373-45-5
Ethanol, 2-[2-(2-hydroxyethoxy)ethoxy]-, 1-(4-Methylbenzenesulfonate)
Triethylene glycol monobenzyl ether
Triethylene glycol
Triethylene glycol monobenzyl ether
Triethylene glycol