CAS 7028-41-3

[1,1′-Biphenyl]-3,5-diol

Description:

[1,1′-Biphenyl]-3,5-diol, with the CAS number 7028-41-3, is an organic compound characterized by its biphenyl structure substituted with hydroxyl groups at the 3 and 5 positions. This compound typically appears as a white to off-white solid and is soluble in organic solvents, but its solubility in water is limited due to its hydrophobic biphenyl backbone. The presence of hydroxyl groups contributes to its potential as a phenolic compound, which can participate in hydrogen bonding and exhibit antioxidant properties. It may also serve as an intermediate in organic synthesis or as a building block in the development of pharmaceuticals and agrochemicals. The compound's chemical stability and reactivity can be influenced by the positioning of the hydroxyl groups, affecting its interaction with other chemical species. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₂H₁₀O₂

InChI: InChI=1S/C12H10O2/c13-11-6-10(7-12(14)8-11)9-4-2-1-3-5-9/h1-8,13-14H

InChI key: InChIKey=UAVUNEWOYVVSEF-UHFFFAOYSA-N

SMILES: OC=1C=C(C=C(O)C1)C2=CC=CC=C2

Synonyms:

• 3,5-Dihydroxybiphenyl
• 3,5-Biphenyldiol
• Resorcinol, 5-phenyl-
• 1,3-Benzenediol, 5-phenyl-
• [1,1′-Biphenyl]-3,5-diol

5-Phenylbenzene-1,3-diol

Controlled Product

CAS: 7028-41-3

Applications 5-phenylbenzene-1,3-diol (cas# 7028-41-3) is a useful research chemical.

Formula: C₁₂H₁₀O₂

Color and Shape: Neat

Molecular weight: 186.21

Ref: TR-P322323

[1,1'-Biphenyl]-3,5-diol

CAS: 7028-41-3

1,1'-Biphenyl-3,5-diol is a fluorescent molecule that belongs to the class of antibiotics. It is used as an alkylating agent and has been shown to be effective in cloning and high yield production of proteins in plants. 1,1'-Biphenyl-3,5-diol has also been shown to have antibiotic properties. It specifically inhibits phytoalexin biosynthesis in plants such as rosaceae, which are susceptible to this type of antibiotic. This drug may be useful in fighting bacteria that have developed resistance to other antibiotics. The 1,1'-biphenyl-3,5-diol molecule reacts with DNA by alkylation at the N7 position of guanine (G) and N4 position of adenine (A). In vitro studies show that this drug is a potent inhibitor of bacterial growth in the presence of oxygen and can inhibit DNA gyrase and topoisomer

Formula: C₁₂H₁₀O₂

Purity: Min. 95%

Molecular weight: 186.21 g/mol

Ref: 3D-HAA02841