886362-15-8

Basic information

• Product Name: 4-AMINO-1-N-BOC-5,7-DICHLORO-1,2,3,4-TETRAHYDROQUINOLINE
• Synonyms: 1(2H)-Quinolinecarboxylic acid, 4-amino-5,7-dichloro-3,4-dihydro-, 1,1-dimethylethyl ester;4-Amino-5,7-dichloro-3,4-dihydro-1(2H)-quinolinecarboxylic acid 1,1-dimethylethyl ester
• CAS NO: 886362-15-8
• Molecular Formula: C14H18Cl2N2O2
• Molecular Weight: 317.214
• Mol File: 886362-15-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 398.8 °C at 760 mmHg
• Flash Point: 195 °C
• Appearance: /
• Density: 1.289 g/cm³
• Vapor Pressure: 1.44E-06mmHg at 25°C
• Refractive Index: 1.565
• CAS DataBase Reference: 4-AMINO-1-N-BOC-5,7-DICHLORO-1,2,3,4-TETRAHYDROQUINOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINO-1-N-BOC-5,7-DICHLORO-1,2,3,4-TETRAHYDROQUINOLINE(886362-15-8)
• EPA Substance Registry System: 4-AMINO-1-N-BOC-5,7-DICHLORO-1,2,3,4-TETRAHYDROQUINOLINE(886362-15-8)

Safety Data

• Hazardous Substances Data: 886362-15-8(Hazardous Substances Data)

Usage

General Description

4-AMINO-1-N-BOC-5,7-DICHLORO-1,2,3,4-TETRAHYDROQUINOLINE is a chemical compound that belongs to the class of tetrahydroquinoline derivatives. It contains an amino group, a BOC (tert-butoxycarbonyl) protecting group, and two chlorine atoms attached to the 5th and 7th positions of the quinoline ring. 4-AMINO-1-N-BOC-5,7-DICHLORO-1,2,3,4-TETRAHYDROQUINOLINE has potential applications in pharmaceutical research and development, particularly in the synthesis of bioactive molecules and drug candidates. The presence of the BOC protecting group allows for selective reactions and manipulations of the amino group, while the chloro substituents can influence the compound's reactivity and biological activity. Further research and studies may elucidate the full potential and uses of 4-AMINO-1-N-BOC-5,7-DICHLORO-1,2,3,4-TETRAHYDROQUINOLINE in various fields of chemistry and drug discovery.

InChI:InChI=1/C14H18Cl2N2O2/c1-14(2,3)20-13(19)18-5-4-10(17)12-9(16)6-8(15)7-11(12)18/h6-7,10H,4-5,17H2,1-3H3