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Home > Encyclopedia > 5-Bromo-8-quinolinamine

5-Bromo-8-quinolinamine

5-Bromo-8-quinolinamine structure

5-Bromo-8-quinolinamine 

structure

5-Bromo-8-quinolinamine Basic Attributes

223.07

223.07

DTXSID60346658

2933499090

Characteristics

38.9

2.6

1.6±0.1 g/cm3

109-110 °C

353.3°C at 760 mmHg

167.5±23.7 °C

1.732

Safety Information

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501

H302

5-Bromo-8-quinolinamine Use and Manufacturing

4.1.16 Quinolin-8-amine (0.20 g, 1.38 μMol) was dissolved in acetonitrile (20 mL), and N-bromosuccinimide (0.26 g, 1.43 μMol) was added to the solution. The mixture was stirred at room temperature for 30 minutes. Water was addedto the mixture. The organic layer was extracted with ethyl acetate, dried over anhydrous sodium sulfate, and concentratedunder reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate = 90/10-> 70/30) to obtain compound 117-1 (0.15 g, 50percent).1H NMR (300 MHz, DMSO-d6, δ): 8.76 (d, J = 3.3 Hz, 1H), 8.42 (d, J = 8.1 Hz, 1H), 7.56 (d, J = 8.4 Hz, 1H), 7.48 (dd, J = 8.4, 4.2 Hz, 1H), 6.80 (d, J = 8.1 Hz, 1H), 5.04 (br, 2H).To a solution of 8-aminoquinoline (1 g, 4.8 mmol) in CH3CN (30 mL) were added NBS (1.28 g, 7.2 mmol). The reaction mixture was stirred at RT for 2 hour. The residue was treated with water and extracted with EA. The extracts were concentrated and the residue purifiled by silica gel chromatography to afford 5-bromo-8-quinolylamine (760 mg).Add 1 magnetic stirrer, In a 500 ml three-necked flask, 10 g (34.8 mmol) of intermediate D and 9.6 g (38.28 mmol) of

Computed Properties

Molecular Weight:223.07
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Exact Mass:221.97926
Monoisotopic Mass:221.97926
Topological Polar Surface Area:38.9
Heavy Atom Count:12
Complexity:163
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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