Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Aldehydes >  8-Quinolinecarbaldehyde

8-Quinolinecarbaldehyde

Basic information Safety Supplier Related

8-Quinolinecarbaldehyde Basic information

Product Name:
8-Quinolinecarbaldehyde
Synonyms:
  • TIMTEC-BB SBB010129
  • RARECHEM AM LA 0004
  • RARECHEM AK ML 0564
  • QUINOLINE-8-CARBALDEHYDE
  • QUINOLINE-8-CARBOXALDEHYDE
  • 8-QUINOLINECARBALDEHYDE
  • 8-QUINOLINECARBOXALDEHYDE
  • ISOQUINOLINE-8-CARBOXALDEHYDE
CAS:
38707-70-9
MF:
C10H7NO
MW:
157.17
Product Categories:
  • Quinolines, Isoquinolines & Quinoxalines
  • quinoline
  • ALDEHYDE
  • Aldehydes
  • Quinolines, Isoquinolines & Quinoxalines
  • Quinoline Derivertives
Mol File:
38707-70-9.mol
More
Less

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
form 
powder to crystal
pka
3.45±0.17(Predicted)
color 
Light orange to Yellow to Green
Water Solubility 
Insoluble in water.
Sensitive 
Air Sensitive
BRN 
113039
InChI
InChI=1S/C10H7NO/c12-7-9-4-1-3-8-5-2-6-11-10(8)9/h1-7H
InChIKey
OVZQVGZERAFSPI-UHFFFAOYSA-N
SMILES
N1C2C(=CC=CC=2C=O)C=CC=1
CAS DataBase Reference
38707-70-9(CAS DataBase Reference)
More
Less

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

  • Language:English Provider:ALFA
More
Less

8-Quinolinecarbaldehyde Usage And Synthesis

Chemical Properties

Off-white solid

Uses

Quinoline-8-carboxaldehyde is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.

Synthesis

16032-35-2

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

8-QuinolinecarbaldehydeSupplier

New Energy Chemicals Gold
Tel
0515-82159099 13770142076
Email
info@njuchem.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com