Tert-butyl 4-amino-5,7-dichloro-3,4-dihydro-2H-quinoline-1-carboxylate is a chemical compound characterized by its complex structure, which includes a quinoline core, amino and carboxylate functional groups, and tert-butyl substituent. This compound features dichlorination at the 5 and 7 positions of the quinoline ring, which can influence its biological activity and solubility. The presence of the tert-butyl group enhances lipophilicity, potentially affecting its pharmacokinetic properties. The amino group may participate in hydrogen bonding, influencing its interactions with biological targets. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, owing to the structural motifs that are often associated with bioactive compounds. Its CAS number, 886362-15-8, allows for precise identification in chemical databases. As with many quinoline derivatives, it may exhibit a range of biological activities, including antimicrobial or anticancer properties, making it a subject of research in various fields, including pharmacology and organic synthesis.

tert-butyl 4-amino-5,7-dichloro-3,4-dihydro-2H-quinoline-1-carboxylate

886362-15-8: Tert-butyl 4-amino-5,7-dichloro-3,4-dihydro-2H-quinoline-1-carboxylate is a chemical compound characterized by its complex structure, which includes a quinoline core, amino and carboxylate functional groups, and tert-butyl substituent. This compound features dichlorination at the 5 and 7 positions of the quinoline ring, which can influence its biological activity and solubility. The presence of the tert-butyl group enhances lipophilicity, potentially affecting its pharmacokinetic properties. The amino group may participate in hydrogen bonding, influencing its interactions with biological targets. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, owing to the structural motifs that are often associated with bioactive compounds. Its CAS number, 886362-15-8, allows for precise identification in chemical databases. As with many quinoline derivatives, it may exhibit a range of biological activities, including antimicrobial or anticancer properties, making it a subject of research in various fields, including pharmacology and organic synthesis.

CAS 886362-15-8

tert-butyl 4-amino-5,7-dichloro-3,4-dihydro-2H-quinoline-1-carboxylate

4-Amino-1-N-Boc-5,7-dichloro-1,2,3,4-tetrahydroquinoline

Ref: IN-DA008AN2

4-Amino-1-N-Boc-5,7-dichloro-1,2,3,4-tetrahydroquinoline

Ref: 10-F041236