2-(Trifluoromethoxy)ethanol, with the CAS number 362631-84-3, is an organic compound characterized by the presence of a trifluoromethoxy group (-OCF3) attached to an ethanol backbone. This compound typically appears as a colorless liquid and is known for its unique properties stemming from the trifluoromethoxy substituent, which imparts significant polarity and potential for hydrogen bonding due to the hydroxyl (-OH) group. The trifluoromethoxy group enhances the compound's stability and can influence its reactivity, making it useful in various chemical applications, including as a solvent or reagent in organic synthesis. Additionally, the presence of fluorine atoms contributes to its low volatility and high thermal stability. The compound's solubility in polar solvents and its relatively low toxicity make it a candidate for use in pharmaceuticals and agrochemicals. However, like many fluorinated compounds, it should be handled with care due to potential environmental and health impacts associated with fluorinated substances.

2-(Trifluoromethoxy)ethanol (CAS: 362631-84-3) is a colorless transparent liquid at room temperature and pressure, and has a certain solubility in water. 2-(Trifluoromethoxy)ethanol is a primary alcohol organic compound, mainly used as an organic synthesis intermediate and a raw material for pharmaceutical production, with the chemical transformation properties of the terminal hydroxyl group of the alkyl chain. This substance can be used to introduce trifluoromethoxy units into the target organic molecular structure. For example, there are literature reports that this substance can be used to synthesize substituted pyridone compounds for the treatment of neuromuscular diseases.

2-(Trifluoromethoxy)ethanol

362631-84-3: 2-(Trifluoromethoxy)ethanol, with the CAS number 362631-84-3, is an organic compound characterized by the presence of a trifluoromethoxy group (-OCF3) attached to an ethanol backbone. This compound typically appears as a colorless liquid and is known for its unique properties stemming from the trifluoromethoxy substituent, which imparts significant polarity and potential for hydrogen bonding due to the hydroxyl (-OH) group. The trifluoromethoxy group enhances the compound's stability and can influence its reactivity, making it useful in various chemical applications, including as a solvent or reagent in organic synthesis. Additionally, the presence of fluorine atoms contributes to its low volatility and high thermal stability. The compound's solubility in polar solvents and its relatively low toxicity make it a candidate for use in pharmaceuticals and agrochemicals. However, like many fluorinated compounds, it should be handled with care due to potential environmental and health impacts associated with fluorinated substances.

CAS 362631-84-3

2-(Trifluoromethoxy)ethanol

2-Hydroxyethyl trifluoromethyl ether

Ref: 54-PC5131

2-Trifluoromethoxy-ethanol

Ref: 10-F075940