CAS 92093-23-7

1-(4-bromophenyl)ethane-1,2-diol

Description:

1-(4-Bromophenyl)ethane-1,2-diol, with the CAS number 92093-23-7, is an organic compound characterized by the presence of a bromophenyl group attached to an ethane backbone that features two hydroxyl (-OH) groups. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It exhibits properties common to diols, such as the ability to form hydrogen bonds, which can influence its solubility in water and organic solvents. The presence of the bromine atom introduces notable reactivity, making it a potential candidate for further chemical transformations, including nucleophilic substitutions or coupling reactions. Additionally, the compound may exhibit biological activity, which could be of interest in medicinal chemistry or material science. Its physical and chemical properties, such as melting point, boiling point, and reactivity, would be influenced by the bromine substituent and the hydroxyl groups, making it a versatile compound in various chemical applications.

1-(4-Bromophenyl)ethane-1,2-diol

CAS: 92093-23-7

Formula: C₈H₉BrO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 217.0599

Ref: IN-DA00IH0N

1-(4-Bromophenyl)ethane-1,2-diol

CAS: 92093-23-7

1-(4-Bromophenyl)ethane-1,2-diol

Purity: 98%

Molecular weight: 217.06g/mol

Ref: 54-OR1033810

1-(4-Bromophenyl)ethane-1,2-diol

CAS: 92093-23-7

Formula: C₈H₉BrO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 217.062

Ref: 10-F238253

1-(4-Bromophenyl)ethane-1,2-diol

Controlled Product

CAS: 92093-23-7

Applications 1-(4-Bromophenyl)ethane-1,2-diol is used as a reactant in the regioselective palladium-catalyzed O,S rearrangement of cyclic thiocarbonates.
References Mahy, William, et al.: Euro. J. of Org. Chem., 2017(43), 6441-6444 (2017)

Formula: C₈H₉BrO₂

Color and Shape: Neat

Molecular weight: 217.06

Ref: TR-B803470