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ChemicalBook >> CAS DataBase List >>6-Quinolinecarbaldehyde

6-Quinolinecarbaldehyde

CAS No.
4113-04-6
Chemical Name:
6-Quinolinecarbaldehyde
Synonyms
QUINOLINE-6-CARBALDEHYDE;6-QUINOLINECARBOXALDEHYDE;inecarbaL;AKOS AUF01714;6-Formylquinoline;AKOS BBS-00005338;6-quinolineMethanal;RARECHEM AK ML 0559;6-QUINOLINECARBALDEHYDE;QUINOLINE-6-CARBOXALDEHYDE
CBNumber:
CB5408618
Molecular Formula:
C10H7NO
Molecular Weight:
157.17
MDL Number:
MFCD00805836
MOL File:
4113-04-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 03:40:26
Product description Number Pack Size Price
6-Quinolinecarboxaldehyde >98.0%(GC)(T) Q0097 1g $110
6-Quinolinecarboxaldehyde >98.0%(GC)(T) Q0097 5g $387
6-Quinolinecarbaldehyde     ≥95% (HPLC) ≥95%(HPLC) 234822 1g $215
6-Quinolinecarbaldehyde     ≥95% (HPLC) ≥95%(HPLC) 234822 5g $360
6-Quinolinecarbaldehyde     ≥95% (HPLC) ≥95%(HPLC) 234822 25g $1217
More product size

6-Quinolinecarbaldehyde Properties

Melting point 74-75°C
Boiling point 314.3±15.0 °C(Predicted)
Density 1.223±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form powder to crystal
pka 4.13±0.10(Predicted)
color White to Yellow to Green
InChI 1S/C10H7NO/c12-7-8-3-4-10-9(6-8)2-1-5-11-10/h1-7H
InChIKey VUAOIXANWIFYCU-UHFFFAOYSA-N
SMILES O=Cc1ccc2ncccc2c1
CAS DataBase Reference 4113-04-6(CAS DataBase Reference)
UNSPSC Code 12352200
NACRES NA.21

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P501-P270-P264-P301+P312+P330
Hazard Codes  Xi
Risk Statements  36/37/38-36/38-36
Safety Statements  26-37/39-36
WGK Germany  WGK 3
HazardClass  IRRITANT
HS Code  29339900
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
NFPA 704
1
2 0

6-Quinolinecarbaldehyde price More Price(65)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical Q0097 6-Quinolinecarboxaldehyde >98.0%(GC)(T) 4113-04-6 1g $110 2026-04-30 Buy
TCI Chemical Q0097 6-Quinolinecarboxaldehyde >98.0%(GC)(T) 4113-04-6 5g $387 2026-04-30 Buy
Usbiological 234822 6-Quinolinecarbaldehyde     ≥95% (HPLC) ≥95%(HPLC) 4113-04-6 1g $215 2026-06-03 Buy
Usbiological 234822 6-Quinolinecarbaldehyde     ≥95% (HPLC) ≥95%(HPLC) 4113-04-6 5g $360 2026-06-03 Buy
Usbiological 234822 6-Quinolinecarbaldehyde     ≥95% (HPLC) ≥95%(HPLC) 4113-04-6 25g $1217 2026-06-03 Buy
Product number Packaging Price Buy
Q0097 1g $110 Buy
Q0097 5g $387 Buy
234822 1g $215 Buy
234822 5g $360 Buy
234822 25g $1217 Buy

6-Quinolinecarbaldehyde Chemical Properties,Uses,Production

Chemical Properties

white to light yellow powde

Synthesis

6-Quinolinylmethanol

100516-88-9

6-Quinolinecarbaldehyde

4113-04-6

General procedure for the synthesis of quinoline-6-carbaldehyde from 6-hydroxymethylquinoline: method adapted from Meyers et al. (Meyers, A. G.; Zhong, B.; Movassaghi, M.; Kung, D. W.; Lanman, B. A.; Kwon, S. Tetrahedron Lett. 2000, 41, 1359-1362). Dess-Martin periodinane (2.57 g, 6.05 mmol) was added to a 0.28 M solution of 6-hydroxymethylquinoline (0.459 g, 2.88 mmol) in water-saturated dichloromethane (10 mL). The reaction mixture was stirred for 10 min and then dichloromethane (3 x 1 mL) was added in batches over 15 min. Subsequently, the reaction mixture was diluted with ether (10 mL) and 80% saturated aqueous sodium bicarbonate solution (10 mL) of sodium thiosulfate (7.87 g, 31.7 mmol) was added. The mixture was stirred rapidly for 45 minutes. The organic and aqueous layers were separated and the aqueous layer was extracted with ether (2 x 20 mL). The combined organic layers were washed sequentially with saturated aqueous sodium bicarbonate solution (30 mL), water (2 x 30 mL) and saturated sodium chloride solution (2 x 30 mL). The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography (30-60% ethyl acetate/hexane) to give 0.383 g (85%) of quinoline-6-carbaldehyde (S4a) as a white solid with a melting point of 76.2-76.5 °C. 1H NMR (400 MHz, CDCl3): δ 7.53 (dd, 1H, J = 4.4, 8.4 Hz), 8.18-8.23 (m, 2H ), 8.33 (dd, 1H, J = 2.0, 8.4 Hz), 8.36 (s, 1H), 9.05 (dd, 1H, J = 2.0, 4.4 Hz), 10.20 (s, 1H).13C NMR (100 MHz, CDCl3): δ 122.4, 126.8, 127.8, 130.9, 133.8, 134.4 , 137.6, 151.0, 153.3, 191.6. HRMS-FAB (m/z): calculated value of 157.0528 for [MH]+ C10H7NO; measured value of 157.0521.

References

[1] Patent: WO2004/7491, 2004, A1. Location in patent: Page 56
[2] Journal of the American Chemical Society, 2008, vol. 130, # 20, p. 6404 - 6410
[3] Patent: WO2009/75778, 2009, A2. Location in patent: Page/Page column 49; 50-51
[4] Patent: US2005/54670, 2005, A1. Location in patent: Page/Page column 27

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View Lastest Price from 6-Quinolinecarbaldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
6-Quinolinecarbaldehyde pictures 2025-12-01 6-Quinolinecarbaldehyde
4113-04-6
1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd

6-Quinolinecarbaldehyde Spectrum

RARECHEM AK ML 0559 6-QUINOLINECARBALDEHYDE AKOS BBS-00005338 AKOS AUF01714 QUINOLINE-6-CARBOXALDEHYDE Quinoline-6-carboxaldehyde 97% 6-Quinolinecarbaldehyde ,97% 6-quinolineMethanal 6-Formylquinoline, 6-Formyl-1-azanaphthalene inecarbaL 6-Formylquinoline 6-Quinolinecarbaldehyde ISO 9001:2015 REACH 6-QUINOLINECARBOXALDEHYDE QUINOLINE-6-CARBALDEHYDE 4113-04-6 808379 808-37-9 4112-04-6 4113-4-6 Quinolines, Isoquinolines & Quinoxalines aldehyde Quinoline Derivertives pharmacetical Aldehydes Quinolines, Isoquinolines & Quinoxalines
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