13669-42-6 | 3-Quinolinecarboxaldehyde

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$6.00	$4.00
1g	98%	in stock	$13.00	$9.00
5g	98%	in stock	$31.00	$22.00
10g	98%	in stock	$59.00	$41.00
25g	98%	in stock	$95.00	$67.00
100g	98%	in stock	$379.00	$265.00

Description

• Catalog Number: AA49340
• Chemical Name: 3-Quinolinecarboxaldehyde
• CAS Number: 13669-42-6
• Molecular Formula: C10H7NO
• Molecular Weight: 157.1687
• MDL Number: MFCD00006768
• SMILES: O=Cc1cnc2c(c1)cccc2

Computed Properties

• Complexity: 169
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 2

Upstream Synthesis Route

3-Quinolinecarboxaldehyde is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. It serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals due to its ability to undergo multiple types of chemical reactions. In organic synthesis, 3-Quinolinecarboxaldehyde is often employed as a precursor for the synthesis of heterocyclic compounds, which are essential in medicinal chemistry and material sciences. Its aldehyde functional group enables the formation of new carbon-carbon bonds through various coupling reactions, such as Wittig olefination, Grignard reaction, and Heck coupling, leading to the creation of complex molecular structures. Additionally, 3-Quinolinecarboxaldehyde's aromatic nature allows it to participate in electrophilic aromatic substitution reactions, providing access to a wide range of substituted quinoline derivatives. Overall, the unique reactivity and functional groups present in 3-Quinolinecarboxaldehyde make it a valuable tool in chemical synthesis for the creation of diverse and structurally complex compounds.

Literature

• Theoretical and experimental studies on the vibrational spectra of 3-quinolinecarboxaldehyde.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120501

• Determination of Imazaquin and its metabolite by liquid chromatography-quadrupole-time of flight tandem mass.

  Bulletin of environmental contamination and toxicology 20100801

• Identification of agonists and antagonists of the human melanocortin-4 receptor from piperazinebenzylamines.

  Bioorganic & medicinal chemistry letters 20050201

• Application of 3-quinolinoyl picket porphyrins to the electroreduction of dioxygen to water: mimicking the active site of cytochrome c oxidase.

  Chembiochem : a European journal of chemical biology 20010202