2,2',4,4',6,6'-Hexamethylbiphenyl, with the CAS number 4482-03-5, is an organic compound belonging to the biphenyl family. It features two phenyl rings connected by a single bond, with six methyl groups attached to the biphenyl structure. This compound is characterized by its high degree of methyl substitution, which influences its physical and chemical properties. It is typically a colorless to pale yellow solid at room temperature and exhibits low solubility in water but is soluble in organic solvents such as benzene and toluene. The presence of multiple methyl groups enhances its hydrophobicity and can affect its melting and boiling points compared to biphenyl. Additionally, 2,2',4,4',6,6'-hexamethylbiphenyl is of interest in various chemical research applications, including studies on molecular interactions and as a potential model compound in the investigation of biphenyl derivatives. Its stability and relatively low reactivity make it suitable for use in various chemical syntheses and applications in materials science.

2,2',4,4',6,6'-hexamethylbiphenyl

4482-03-5: 2,4,6,2',4',6'-Hexamethylbiphenyl, Bimesityl, Biphenyl, 2,2',4,4',6,6'-hexamethyl-

2,2',4,4',6,6'-HEXAMETHYL-1,1'-BIPHENYL

2,2',4,4',6,6'-Hexamethyl-1,1'-biphenyl

2,2',4,4',6,6'-Hexamethyl-1,1'-biphenyl is a biphenyl compound that exists as a colorless liquid at room temperature. It has electronic interactions with other molecules and can undergo protonation. 2,2',4,4',6,6'-Hexamethyl-1,1'-biphenyl can be used to make sulfonanilides and carbon tetrachloride. This chemical also reacts with hydrogen chloride to produce 2-chloroethanol and chloroform. The molecule has an amide bond that is susceptible to hydrolysis by base or acid.

CAS 4482-03-5: 2,2',4,4',6,6'-hexamethylbiphenyl

2,2',4,4',6,6'-HEXAMETHYL-1,1'-BIPHENYL

Ref: 10-F542351

2,2',4,4',6,6'-Hexamethyl-1,1'-biphenyl

Ref: IN-DA003D7N

2,2',4,4',6,6'-Hexamethyl-1,1'-biphenyl

Ref: 3D-EAA48203