Tert-butyl 2,2-dimethylquinoline-1(2H)-carboxylate is an organic compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom in the ring. This substance features a tert-butyl group and a carboxylate functional group, contributing to its solubility and reactivity. The presence of the dimethyl substituents on the quinoline ring influences its steric and electronic properties, potentially affecting its interactions in chemical reactions. Typically, compounds like this may exhibit moderate to high lipophilicity due to the bulky tert-butyl group, which can enhance their ability to penetrate biological membranes. Additionally, the carboxylate moiety may participate in hydrogen bonding and ionic interactions, making it relevant in various chemical and biological applications. The compound's unique structure may also confer specific optical or electronic properties, which could be exploited in fields such as materials science or medicinal chemistry. Overall, tert-butyl 2,2-dimethylquinoline-1(2H)-carboxylate represents a versatile building block in organic synthesis and drug development.

tert-butyl 2,2-dimethylquinoline-1(2H)-carboxylate

179898-89-6: Tert-butyl 2,2-dimethylquinoline-1(2H)-carboxylate is an organic compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom in the ring. This substance features a tert-butyl group and a carboxylate functional group, contributing to its solubility and reactivity. The presence of the dimethyl substituents on the quinoline ring influences its steric and electronic properties, potentially affecting its interactions in chemical reactions. Typically, compounds like this may exhibit moderate to high lipophilicity due to the bulky tert-butyl group, which can enhance their ability to penetrate biological membranes. Additionally, the carboxylate moiety may participate in hydrogen bonding and ionic interactions, making it relevant in various chemical and biological applications. The compound's unique structure may also confer specific optical or electronic properties, which could be exploited in fields such as materials science or medicinal chemistry. Overall, tert-butyl 2,2-dimethylquinoline-1(2H)-carboxylate represents a versatile building block in organic synthesis and drug development.

CAS 179898-89-6

tert-butyl 2,2-dimethylquinoline-1(2H)-carboxylate

tert-butyl 2,2-dimethyl-1,2-dihydroquinoline-1-carboxylate

Ref: IN-DA0027CE

tert-Butyl 2,2-dimethyl-1,2-dihydroquinoline-1-carboxylate

Ref: 3D-EHA89889