CAS 1250113-83-7

1-(2,4,6-trifluorophenyl)alcohol

Description:

1-(2,4,6-Trifluorophenyl)alcohol is an organic compound characterized by the presence of a trifluorinated phenyl group attached to a hydroxyl (-OH) functional group. This compound features a phenolic structure, where the trifluoromethyl groups significantly influence its chemical properties, including increased acidity and potential for hydrogen bonding. The trifluoromethyl substituents enhance the compound's lipophilicity and can affect its reactivity and interaction with biological systems. Typically, such compounds exhibit unique solubility characteristics, often being soluble in organic solvents while having limited solubility in water due to the hydrophobic nature of the fluorinated groups. The presence of fluorine atoms can also impart stability against oxidation and degradation, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. Additionally, the compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the fluorine atoms, which can influence its behavior in chemical reactions and interactions with other molecules.

1-(2,4,6-trifluorophenyl)ethan-1-ol

CAS: 1250113-83-7

Formula: C₈H₇F₃O

Purity: 97%

Color and Shape: Liquid

Molecular weight: 176.1358

Ref: IN-DA01A1LL

1-(2,4,6-Trifluorophenyl)ethanol

CAS: 1250113-83-7

1-(2,4,6-Trifluorophenyl)ethanol

Purity: 97%

Molecular weight: 176.14g/mol

Ref: 54-PC103677

1-(2,4,6-Trifluorophenyl)ethanol

CAS: 1250113-83-7

Formula: C₈H₇F₃O

Purity: 97%

Molecular weight: 176.138

Ref: 10-F544738

1-(2,4,6-Trifluorophenyl)ethanol

CAS: 1250113-83-7

1-(2,4,6-Trifluorophenyl)ethanol is a monomer that can be used in the production of polymers with high thermal stability. It is obtained by copolymerizing ethylene and styrene, which contain fluorine atoms. 1-(2,4,6-Trifluorophenyl)ethanol exhibits a transition temperature of -10°C to 10°C and has been shown to have a large degree of polymerization. The acetaldehyde produced during the dehydration reaction is converted into acetic acid by dilution with water. The cross-coupling reaction between 1-(2,4,6-trifluorophenyl)ethanol and other molecules is possible due to the presence of fluorine atoms on the molecule's structure. This monomer also has a square shape that makes it easy to use for polymerization reactions because it does not form coils or rings.

Formula: C₈H₇F₃O

Purity: Min. 95%

Molecular weight: 176.14 g/mol

Ref: 3D-AAC11383