580-17-6 | 3-Aminoquinoline

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$15.00	$10.00
1g	95%	in stock	$26.00	$18.00
5g	97%	in stock	$58.00	$41.00
25g	97%	in stock	$187.00	$131.00
100g	97%	in stock	$628.00	$440.00
500g	97%	in stock	$2,314.00	$1,620.00

Description

• Catalog Number: AB49040
• Chemical Name: 3-Aminoquinoline
• CAS Number: 580-17-6
• Molecular Formula: C9H8N2
• Molecular Weight: 144.1732
• MDL Number: MFCD00006772
• SMILES: Nc1cnc2c(c1)cccc2
• NSC Number: 7934

Computed Properties

• Complexity: 136
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.6

Literature

• Photoacoustic and luminescence characterization of nitrogen heterocyclic aromatic UV-MALDI matrices in solution.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20120601

• Sodium cation affinities of commonly used MALDI matrices determined by guided ion beam tandem mass spectrometry.

  Journal of the American Society for Mass Spectrometry 20120401

• Detailed structural analysis of lipids directly on tissue specimens using a MALDI-SpiralTOF-Reflectron TOF mass spectrometer.

  PloS one 20120101

• The effect of N-methylation on photophysical properties of 3-aminoquinoline.

  Journal of fluorescence 20110901

• The mechanism of boron mobility in wheat and canola phloem.

  Plant physiology 20100601

• 3-Aminoquinoline acting as matrix and derivatizing agent for MALDI MS analysis of oligosaccharides.

  Analytical chemistry 20100501

• Evaluation of Fructooligosaccharides and Inulins as Potentially Health Benefiting Food Ingredients by HPAEC-PED and MALDI-TOF MS.

  International journal of analytical chemistry 20090101

• Gene expression signatures and small-molecule compounds link a protein kinase to Plasmodium falciparum motility.

  Nature chemical biology 20080601

• Comparison of mass spectra of peptides in different matrices using matrix-assisted laser desorption/ionization and a multi-turn time-of-flight mass spectrometer, MULTUM-IMG.

  Rapid communications in mass spectrometry : RCM 20080501

• The role of the ring nitrogen and the amino group in the solvent dependence of the excited-state dynamics of 3-aminoquinoline.

  The Journal of chemical physics 20060807

• Prediction of genotoxicity of chemical compounds by statistical learning methods.

  Chemical research in toxicology 20050601

• Water-soluble benzoheterocycle triosmium clusters as potential inhibitors of telomerase enzyme.

  Journal of inorganic biochemistry 20050201

• A technique for obtaining matrix-assisted laser desorption/ionization time-of-flight mass spectra of poorly soluble and insoluble aromatic polyamides.

  Analytical chemistry 20040401

• Analysis of a bioactive beta-(1 --> 3) polysaccharide (Curdlan) using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

  Rapid communications in mass spectrometry : RCM 20030101

• Characterization of an insoluble polyimide oligomer by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

  Rapid communications in mass spectrometry : RCM 20020101

• Synthesis of 2-substituted trifluoromethylquinolines for the evaluation of leishmanicidal activity.

  Chemical & pharmaceutical bulletin 20010401