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Home > Encyclopedia > 6-Quinolinecarboxylic acid

6-Quinolinecarboxylic acid

6-Quinolinecarboxylic acid structure

6-Quinolinecarboxylic acid 

structure

Description

beige to brown crystalline powder

6-Quinolinecarboxylic acid Basic Attributes

173.17

173.17

233-761-4

DTXSID7065047

29334900

Characteristics

50.2

1.3

Beige to brown Crystalline Powder

1.2427 (rough estimate)

291 °C

303.81°C (rough estimate)

164.7±20.9 °C

1.5200 (estimate)

0.90 M

Store in a cool, dry place. Keep container closed when not in use.

1.85E-05mmHg at 25°C

Safety Information

IRRITANT

36/37/38

37/39-26

Xi

Irritant

Stable under normal temperatures and pressures.

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

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 6 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

6-Quinolinecarboxylic acid Use and Manufacturing

Methods of Manufacturing

To a solution of 6-methylquinoline (100.0 mg, 0.70 mmol) in HStep 1.Step 1:To a mixture of 4-aminobenzoic acid (175 g, 1.28 mol), 4-nitrophenol (88.75 g, 0.64 mol) and sulphuric acid (1.2 lit.), glycerol (234.8 g, 2.55 mol) was added dropwise at 135°C. After 48h, the reaction mixture was cooled to 0°C and the pH adjusted to 3-5 with 10percent sodium hydroxide solution. The resulting precipitate was collected by filtration and washed with water and dried under vacuum to afford the title compound as a black solid (125 g, 56percent).[252] Intermediates Intermediate 1: Quinolin-6-ylmethanamine: Stepl : Quinoline-6-carboxylic acid: To a mixture of 4-aminobenzoic acid: (175 g, 1.28 mol), 4-nitrophenol (88.75 g, 0.64 mol) and sulphuric acid (1.2 lit.), glycerol (234.8 g, 2.55 mol) was added drop wise at 135°C. After 48h, the reaction mixture was cooled to 0°C and the pH adjusted to 3-5 with 10percent sodium hydroxide solution. The resulting precipitate was collected by filtration and washed with water and dried under vacuum to afford the title compound as a black solid (125 g, 56percent).Step 1:

6-Quinolinecarboxylic acid: ACTIVE

Computed Properties

Molecular Weight:173.17
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:173.047678466
Monoisotopic Mass:173.047678466
Topological Polar Surface Area:50.2
Heavy Atom Count:13
Complexity:205
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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