Phenol, 2-ethenyl-6-methyl- (CAS 135295-09-9) is an organic compound characterized by a phenolic structure with a vinyl group and a methyl substituent. This compound features a hydroxyl (-OH) group attached to a benzene ring, which contributes to its acidic properties and reactivity. The presence of the ethenyl group introduces unsaturation, making it more reactive in various chemical reactions, such as polymerization and electrophilic substitution. The methyl group at the 6-position influences the compound's steric and electronic properties, potentially affecting its reactivity and interactions with other molecules. Phenolic compounds are known for their antioxidant properties and can participate in hydrogen bonding, which may affect their solubility in different solvents. Additionally, the compound may exhibit biological activity, making it of interest in fields such as pharmaceuticals and materials science. Overall, the unique structure of 2-ethenyl-6-methyl-phenol contributes to its diverse chemical behavior and potential applications.

Phenol, 2-ethenyl-6-methyl-

135295-09-9: Phenol, 2-ethenyl-6-methyl- (CAS 135295-09-9) is an organic compound characterized by a phenolic structure with a vinyl group and a methyl substituent. This compound features a hydroxyl (-OH) group attached to a benzene ring, which contributes to its acidic properties and reactivity. The presence of the ethenyl group introduces unsaturation, making it more reactive in various chemical reactions, such as polymerization and electrophilic substitution. The methyl group at the 6-position influences the compound's steric and electronic properties, potentially affecting its reactivity and interactions with other molecules. Phenolic compounds are known for their antioxidant properties and can participate in hydrogen bonding, which may affect their solubility in different solvents. Additionally, the compound may exhibit biological activity, making it of interest in fields such as pharmaceuticals and materials science. Overall, the unique structure of 2-ethenyl-6-methyl-phenol contributes to its diverse chemical behavior and potential applications.