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8-Quinolinecarbaldehyde

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8-Quinolinecarbaldehyde manufacturers

8-Quinolinecarbaldehyde Basic information
Product Name:8-Quinolinecarbaldehyde
Synonyms:TIMTEC-BB SBB010129;RARECHEM AM LA 0004;RARECHEM AK ML 0564;QUINOLINE-8-CARBOXALDEHYDE;8-QUINOLINECARBALDEHYDE;8-QUINOLINECARBOXALDEHYDE;ISOQUINOLINE-8-CARBOXALDEHYDE;ISOQUINOLINE-8-CARBALDEHYDE
CAS:38707-70-9
MF:C10H7NO
MW:157.17
EINECS:
Product Categories:Quinolines, Isoquinolines & Quinoxalines;quinoline;ALDEHYDE;Aldehydes;Quinolines, Isoquinolines & Quinoxalines;Quinoline Derivertives
Mol File:38707-70-9.mol
8-Quinolinecarbaldehyde Structure
8-Quinolinecarbaldehyde Chemical Properties
Melting point 95-96°C
Boiling point 314.3±15.0 °C(Predicted)
density 1.223±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka3.45±0.17(Predicted)
form powder to crystal
color Light orange to Yellow to Green
Water Solubility Insoluble in water.
Sensitive Air Sensitive
BRN 113039
InChIInChI=1S/C10H7NO/c12-7-9-4-1-3-8-5-2-6-11-10(8)9/h1-7H
InChIKeyOVZQVGZERAFSPI-UHFFFAOYSA-N
SMILESN1C2C(=CC=CC=2C=O)C=CC=1
CAS DataBase Reference38707-70-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-36/38-43
Safety Statements 26-37/39-36/37
HazardClass IRRITANT
HS Code 29334900
MSDS Information
ProviderLanguage
ALFA English
8-Quinolinecarbaldehyde Usage And Synthesis
Chemical PropertiesOff-white solid
UsesQuinoline-8-carboxaldehyde is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.
Synthesis
8-Quinolinemethanol

16032-35-2

8-Quinolinecarbaldehyde

38707-70-9

General method: 8-quinoline methanol was dissolved in anhydrous DMSO (10 v/v), 1 equivalent of polymer bromide was added, and the reaction mixture was stirred at room temperature for the indicated time (see Table 1). Upon completion of the reaction, the mixture was filtered and the polymer bed was washed with DMSO. The DMSO layers were combined and the reaction was quenched with an ice-water mixture and subsequently extracted with ether. The ether layer was washed sequentially with water and brine, dried over anhydrous sodium sulfate and concentrated to give pure 8-quinolinecarboxaldehyde. All products were structurally confirmed by nuclear magnetic resonance (NMR) and mass spectrometry (MS).

References[1] Tetrahedron Letters, 2011, vol. 52, # 51, p. 6971 - 6973
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 10, p. 3480 - 3484
[3] Angewandte Chemie - International Edition, 2016, vol. 55, # 31, p. 9084 - 9087
[4] Angew. Chem., 2016, vol. 128, # 31, p. 9230 - 9233,4
Tag:8-Quinolinecarbaldehyde(38707-70-9) Related Product Information
Quinoline Yellow Isoquinoline 8-Hydroxyquinoline 2-Quinolinecarboxaldehyde Quinhydrone 6-Hydroxy-2(1H)-3,4-dihydroquinolinone Quinclorac Formaldehyde Ethoxyquin quinoline-2-carboxiMidaMide hydrochloride 8-Quinolineboronic acid Quinoline sulphate 8-acetylquinoline 8-Hydroxyquinoline-2-carboxaldehyde Isoquinoline-1-carbaldehyde Isoquinoline-8-carbaldehyde 2-Oxo-1,2-dihydro-quinoline-3-carbaldehyde 8-Quinolinecarboxylic acid