Weight | 157.172 g/mol |
---|---|
Formula | C10H7NO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 1 |
4-Quinolinecarboxaldehyde (4363-93-3)
quinoline-4-carbaldehyde
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- Design of 3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde as a reagent for ultrasensitive determination of primary amines by capillary electrophoresis using laser fluorescence detection (Analytical Chemistry, 1991)
- Sensitive determination of biogenic amines by capillary electrophoresis with a new fluorogenic reagent 3-(4-fluorobenzoyl)-2-quinolinecarboxaldehyde (Talanta, 2008)
- Separation of free amino acids and catecholamines in human plasma and rabbit vitreous samples using a new fluorogenic reagent 3-(4-bromobenzoyl)-2-quinolinecarboxaldehyde with CE-LIF detection. (Electrophoresis, 2009)
- Determination of amino acids and catecholamines derivatized with 3-(4-chlorobenzoyl)-2-quinolinecarboxaldehyde in PC12 and HEK293 cells by capillary electrophoresis with laser-induced fluorescence detection (Analytical and Bioanalytical Chemistry, 2011)
- Synthesis of Novel (Acyloxy)(quinolin4yl)acetamides by a ThreeComponent Reaction between an Isocyanide, Quinoline4carbaldehyde, and Arenecarboxylic Acids (Helvetica Chimica Acta, 2014)
- Vibrational spectra of quinoline-4-carbaldehyde: Combined experimental and theoretical studies (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2013)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - quinoline-4-carbaldehyde
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SMILESC1=CC=C2C(=C1)C(=CC=N2)C=O
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InChIKeyMGCGJBXTNWUHQE-UHFFFAOYSA-N
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