4-Butyl-4'-bromobiphenyl is an organic compound characterized by its biphenyl structure, where a butyl group and a bromine atom are substituted on the phenyl rings. This compound typically exhibits a white to pale yellow crystalline appearance. It has a relatively high melting point, indicative of strong intermolecular interactions, likely due to the presence of the bromine atom, which can engage in halogen bonding. The butyl group contributes to its hydrophobic character, influencing its solubility in organic solvents while rendering it less soluble in water. 4-Butyl-4'-bromobiphenyl is often utilized in organic synthesis and materials science, particularly in the development of liquid crystals and as a potential intermediate in the synthesis of other chemical compounds. Its bromine substituent can also participate in various chemical reactions, such as nucleophilic substitutions. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks. Overall, this compound exemplifies the diverse functionalities that can arise from simple structural modifications in organic chemistry.

4-Butyl-4'-bromobiphenyl

63619-54-5: 4-Butyl-4'-bromobiphenyl is an organic compound characterized by its biphenyl structure, where a butyl group and a bromine atom are substituted on the phenyl rings. This compound typically exhibits a white to pale yellow crystalline appearance. It has a relatively high melting point, indicative of strong intermolecular interactions, likely due to the presence of the bromine atom, which can engage in halogen bonding. The butyl group contributes to its hydrophobic character, influencing its solubility in organic solvents while rendering it less soluble in water. 4-Butyl-4'-bromobiphenyl is often utilized in organic synthesis and materials science, particularly in the development of liquid crystals and as a potential intermediate in the synthesis of other chemical compounds. Its bromine substituent can also participate in various chemical reactions, such as nucleophilic substitutions. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks. Overall, this compound exemplifies the diverse functionalities that can arise from simple structural modifications in organic chemistry.

CAS 63619-54-5

4-Butyl-4'-bromobiphenyl

4-Bromo-4'-butyl-1,1'-biphenyl

Ref: 54-OR1007662

4-Bromo-4′-butyl-1,1′-biphenyl

Ref: 10-F232310

1,1'-BIPHENYL, 4-BROMO-4'-BUTYL-

Ref: IN-DA00EB89