4-Quinolinecarboxaldehyde
- Product Name
- 4-Quinolinecarboxaldehyde
- CAS No.
- 4363-93-3
- Chemical Name
- 4-Quinolinecarboxaldehyde
- Synonyms
- QUINOLINE-4-CARBALDEHYDE;4-fomylquinoline;4-FORMYLQUINOLINE;AKOS BBS-00005334;CINCHONINALDEHYDE;TIMTEC-BB SBB004008;RARECHEM AQ NN 0218;4-Quinolinealdehyde;QUINOLINE-4-ALDEHYDE;4-QUINOLINECARBALDEHYDE
- CBNumber
- CB4773795
- Molecular Formula
- C10H7NO
- Formula Weight
- 157.17
- MOL File
- 4363-93-3.mol
4-Quinolinecarboxaldehyde Property
- Melting point:
- 45-52 °C (lit.)
- Boiling point:
- 131-133°C 5mm
- Density
- 1.1599 (rough estimate)
- refractive index
- 1.5000 (estimate)
- Flash point:
- >230 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- pka
- 2.95±0.13(Predicted)
- form
- Crystalline Powder, Chunks, or Solid
- color
- Off-white to yellow-brown
- Water Solubility
- Slightly soluble in water.
- Sensitive
- Air Sensitive
- BRN
- 113072
- InChI
- InChI=1S/C10H7NO/c12-7-8-5-6-11-10-4-2-1-3-9(8)10/h1-7H
- InChIKey
- MGCGJBXTNWUHQE-UHFFFAOYSA-N
- SMILES
- N1C2C(=CC=CC=2)C(C=O)=CC=1
- CAS DataBase Reference
- 4363-93-3(CAS DataBase Reference)
Safety
- Hazard Codes
- Xi
- Risk Statements
- 37/38-36/37/38
- Safety Statements
- 24/25-36-26-36/37/39
- WGK Germany
- 3
- F
- 10
- HazardClass
- IRRITANT
- HS Code
- 29334900
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
N-Bromosuccinimide Price
- Product number
- 176966
- Product name
- 4-Quinolinecarboxaldehyde
- Purity
- 97%
- Packaging
- 2.5g
- Price
- $75.3
- Updated
- 2025/07/31
- Product number
- 176966
- Product name
- 4-Quinolinecarboxaldehyde
- Purity
- 97%
- Packaging
- 10g
- Price
- $246
- Updated
- 2025/07/31
- Product number
- Q0061
- Product name
- 4-Quinolinecarboxaldehyde
- Purity
- >97.0%(GC)(T)
- Packaging
- 1g
- Price
- $38
- Updated
- 2025/07/31
- Product number
- Q0061
- Product name
- 4-Quinolinecarboxaldehyde
- Purity
- >97.0%(GC)(T)
- Packaging
- 5g
- Price
- $103
- Updated
- 2025/07/31
- Product number
- Q0061
- Product name
- 4-Quinolinecarboxaldehyde
- Purity
- >97.0%(GC)(T)
- Packaging
- 25g
- Price
- $348
- Updated
- 2025/07/31
4-Quinolinecarboxaldehyde Chemical Properties,Usage,Production
Chemical Properties
yellow to yellow-brown crystalline powder
Occurrence
The common presence of 4-quinolinecarboxaldehyde in honey from Galicia (northwest of Spain). As opposed to other quinoline carboxylic acid derivatives, the 4- quinolinecarboxaldehyde species has not been correlated with the anti-diabetic properties of honey; nevertheless, it appears to be active against intestinal bacteria.
Uses
4-Quinolinecarboxaldehyde was used in the synthesis of lepidylamines. It also shows antimicrobial activity toward human intestinal bacteria such as Clostridium perfringens.
Synthesis Reference(s)
The Journal of Organic Chemistry, 35, p. 841, 1970 DOI: 10.1021/jo00828a074
Synthesis
491-35-0
4363-93-3
The general procedure for the synthesis of 4-quinolinecarboxaldehyde from 4-methylquinoline was as follows: 5.0 g (35 mmol) of 4-methylquinoline and 5.0 g (45 mmol) of selenium dioxide were dissolved in toluene under argon protection and heated to reflux for 24 hours. After completion of the reaction, the reaction mixture was diluted with dichloromethane, washed sequentially with saturated saline and dried with anhydrous magnesium sulfate. After concentration under reduced pressure, the reaction was purified by silica gel column chromatography using a solvent mixture of hexane and ethyl acetate (4:1, v/v) as eluent to give 4.0 g (73% yield) of the target product 4-quinolinecarboxaldehyde as a solid. Nuclear magnetic resonance hydrogen spectroscopy (1H NMR) data: δ 10.54 (s, 1H), 9.22 (d, J = 4.3 Hz, 1H), 9.04 (d, J = 8.6 Hz, 1H), 8.24 (d, J = 8.2 Hz, 1H), 7.84 (t, J = 7.6 Hz, 1H), 7.81 (d, J = 4.3 Hz, 1H), 7.76 (t , J = 8.0 Hz, 1H). Nuclear magnetic resonance carbon (13C NMR) data: δ 193.1, 150.7, 149.5, 137.0, 130.4, 130.3, 129.6, 126.0, 124.7, 124.1. mass spectrometry (electrospray ionization) data: m/z 158.0 (100%) ([M + H]+), 130.2.
References
[1] Tamara Rodríguez-Cabo. “Time-of-flight accurate mass spectrometry identification of quinoline alkaloids in honey.” Analytical and Bioanalytical Chemistry 407 20 (2015): 6159–6170.
4-Quinolinecarboxaldehyde Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 4-Quinolinecarboxaldehyde manufacturers
- Product
- 4-Quinolinecarboxaldehyde 4363-93-3
- Price
- US $0.00-0.00/KG
- Min. Order
- 1KG
- Purity
- 98.0%
- Supply Ability
- 10000KGS
- Release date
- 2025-06-03
- Product
- 4-Quinolinecarbaldehyde 4363-93-3
- Price
- US $15.00-10.00/KG
- Min. Order
- 1KG
- Purity
- 99%+ HPLC
- Supply Ability
- Monthly supply of 1 ton
- Release date
- 2021-07-08
- Product
- 4-Quinolinecarboxaldehyde 4363-93-3
- Price
- US $1.00/kg
- Min. Order
- 1kg
- Purity
- 98%
- Supply Ability
- 100KG
- Release date
- 2018-12-22