[1,1′-Biphenyl]-3,4-diol, also known as 3,4-dihydroxybiphenyl, is an organic compound characterized by the presence of two phenyl rings connected by a single bond, with hydroxyl (-OH) groups attached to the 3rd and 4th positions of one of the rings. This compound typically appears as a white to light yellow solid and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water due to its hydrophobic biphenyl structure. It exhibits properties typical of phenolic compounds, including the ability to participate in hydrogen bonding and act as an antioxidant. The presence of hydroxyl groups contributes to its reactivity, allowing it to undergo various chemical transformations, such as oxidation and substitution reactions. Additionally, [1,1′-Biphenyl]-3,4-diol has potential applications in organic synthesis and materials science, particularly in the development of dyes, pharmaceuticals, and polymers. Safety data indicates that, like many phenolic compounds, it should be handled with care due to potential toxicity and irritant properties.

[1,1′-Biphenyl]-3,4-diol

92-05-7: [1,1′-Biphenyl]-3,4-diol, also known as 3,4-dihydroxybiphenyl, is an organic compound characterized by the presence of two phenyl rings connected by a single bond, with hydroxyl (-OH) groups attached to the 3rd and 4th positions of one of the rings. This compound typically appears as a white to light yellow solid and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water due to its hydrophobic biphenyl structure. It exhibits properties typical of phenolic compounds, including the ability to participate in hydrogen bonding and act as an antioxidant. The presence of hydroxyl groups contributes to its reactivity, allowing it to undergo various chemical transformations, such as oxidation and substitution reactions. Additionally, [1,1′-Biphenyl]-3,4-diol has potential applications in organic synthesis and materials science, particularly in the development of dyes, pharmaceuticals, and polymers. Safety data indicates that, like many phenolic compounds, it should be handled with care due to potential toxicity and irritant properties.

4-phenylbenzene-1,2-diol

CAS 92-05-7

[1,1′-Biphenyl]-3,4-diol

4-phenylbenzene-1,2-diol

Ref: IN-DA003AW2

[1,1′-biphenyl]-3,4-diol

Ref: 10-F653470