CAS 5470-96-2

2-Quinolinecarboxaldehyde

Description:

2-Quinolinecarboxaldehyde, with the CAS number 5470-96-2, is an organic compound that features a quinoline ring structure with an aldehyde functional group at the second position. This compound is characterized by its aromatic nature, which contributes to its stability and reactivity. It typically appears as a yellow to brown liquid or solid, depending on the specific conditions and purity. The presence of the aldehyde group makes it a versatile intermediate in organic synthesis, allowing for various chemical reactions, including condensation and oxidation. 2-Quinolinecarboxaldehyde is also known for its potential biological activities, which may include antimicrobial and antitumor properties, making it of interest in medicinal chemistry. Its solubility in organic solvents and limited solubility in water further define its chemical behavior. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested. Overall, 2-Quinolinecarboxaldehyde is a significant compound in both synthetic and medicinal chemistry contexts.

Formula: C₁₀H₇NO

InChI: InChI=1S/C10H7NO/c12-7-9-6-5-8-3-1-2-4-10(8)11-9/h1-7H

InChI key: InChIKey=WPYJKGWLDJECQD-UHFFFAOYSA-N

SMILES: C(=O)C1=NC2=C(C=C1)C=CC=C2

Synonyms:

• 2-Formylquinoline
• 2-Quinolinecarbaldehyde
• 2-Quinolylaldehyde
• 2-Quinolylcarbaldehyde
• NSC 27026
• Quinaldaldehyde
• Quinaldehyde
• Quinoline-2-Carbaldehyde
• Quinoline-2-carboxaldehyde
• Timtec-Bb Sbb004007
• 2-Quinolinecarboxaldehyde

2-Quinolinecarboxaldehyde

CAS: 5470-96-2

Formula: C₁₀H₇NO

Purity: >97.0%(GC)

Color and Shape: Light yellow to Brown powder to crystal

Molecular weight: 157.17

Ref: 3B-Q0064

Quinoline-2-carboxaldehyde, 97%

CAS: 5470-96-2

2-Quinolinecarboxaldehyde was used in the preparation of 3-(2-quinolyl)-1-phenyl-2-propenone via rapid, tandem aldol-Michael reactions with the lithium, sodium and potassium enolates of acetophenone; imine-type ligands; sugar-quinoline fluorescent sensor for the detection of Hg2+ in natural water.

Formula: C₁₀H₇NO

Purity: 97%

Color and Shape: Crystals or powder or crystalline powder, Yellow to orange to brown

Molecular weight: 157.17

Ref: 02-L20202

2-Quinolinecarboxaldehyde

CAS: 5470-96-2

Formula: C₁₀H₇NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 157.1687

Ref: IN-DA0033FU

2-Quinolinecarboxaldehyde

CAS: 5470-96-2

Formula: C₁₀H₇NO

Molecular weight: 157.17

Ref: 7W-GK3124

2-Quinolinecarboxaldehyde

CAS: 5470-96-2

2-Quinolinecarboxaldehyde

Purity: ≥98%

Molecular weight: 157.17g/mol

Ref: 54-BUP16012

2-Quinolinecarboxaldehyde

CAS: 5470-96-2

2-Quinolinecarboxaldehyde, a small rigid molecule, used in Henry reaction, inhibits AChE (IC50: 13.48 μM).

Formula: C₁₀H₇NO

Purity: 99.5%

Color and Shape: Off-White Crystalline

Molecular weight: 157.17

Ref: TM-T72028

Quinoline-2-carboxaldehyde

CAS: 5470-96-2

Quinoline-2-carboxaldehyde

Formula: C₁₀H₇NO

Purity: 98%

Color and Shape: light orange solid

Molecular weight: 157.17g/mol

Ref: 54-OR23073

Quinoline-2-carboxaldehyde

CAS: 5470-96-2

Purity: 98%

Molecular weight: 157.17

Ref: 10-F790896