529-89-5

Basic information

• Product Name: 2,4-DIHYDROXY-3-FORMYLQUINOLINE
• Synonyms: NORDICTAMNAL;2,4-DIHYDROXY-3-FORMYLQUINOLINE;2,4-DIHYDROXY-3-QUINOLINECARBOXALDEHYDE;3-FORMYL-2,4-DIHYDROXYQUINOLINE;. Nordictamnal 2,4-Dihydroxy-3-quinolinecarboxaldehyde 3-Formyl-2,4-dihydroxyquinoline;3-Quinolinecarboxaldehyde, 2, 4-dihydroxy-;4-Hydroxy-2-oxo-1,2-dihydro-quinoline-3-carbaldehyde
• CAS NO: 529-89-5
• Molecular Formula: C₁₀H₇NO₃
• Molecular Weight: 189.17
• Mol File: 529-89-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 393.9 °C at 760 mmHg
• Flash Point: 192 °C
• Appearance: /
• Density: 1.509 g/cm³
• Vapor Pressure: 2.87E-08mmHg at 25°C
• Refractive Index: 1.74
• CAS DataBase Reference: 2,4-DIHYDROXY-3-FORMYLQUINOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-DIHYDROXY-3-FORMYLQUINOLINE(529-89-5)
• EPA Substance Registry System: 2,4-DIHYDROXY-3-FORMYLQUINOLINE(529-89-5)

Safety Data

• Hazardous Substances Data: 529-89-5(Hazardous Substances Data)

Usage

General Description

2,4-Dihydroxy-3-formylquinoline is a chemical compound with the molecular formula C10H7NO3. It is a yellowish-brown solid and is used in the synthesis of a variety of organic compounds. This chemical is known for its ability to act as an intermediate in the biosynthesis of the natural product, yohimbine. It also has potential applications in the pharmaceutical industry as a precursor for the synthesis of bioactive molecules. Additionally, 2,4-dihydroxy-3-formylquinoline has antioxidant properties and has shown promise in studies for its potential therapeutic effects.

InChI:InChI=1/C10H7NO3/c12-5-7-9(13)6-3-1-2-4-8(6)11-10(7)14/h1-5,12H,(H,11,14)/b7-5-

Upstream product

• 62-53-3 aniline 
• 70254-43-2 4-Hydroxy-2-quinolone 
• 67-66-3 chloroform 
• 59856-27-8 3-[(phenylamino)methylene]quinoline-2,4(1H,3H)-dione 
• 70254-44-3 2,4-dihydroxyquinoline 
• 148586-97-4 3-[1-(2,6-Dimethyl-phenylamino)-meth-(Z)-ylidene]-1H-quinoline-2,4-dione 

Downstream Products

• 1190084-56-0 C₁₇H₁₄N₂O₂ 
• 1190084-54-8 C₁₆H₁₁N₃O₄ 
• 1190084-53-7 C₁₆H₁₁N₃O₄ 
• 55567-59-4 3-phenyliminomethyl-4-hydroxy-2-quinolone 
• 1190084-55-9 C₁₇H₁₄N₂O₂ 
• 81115-80-2 3-anilino-2,3-dihydrofuro<3,2-c>quinolin-4(5H)-one 
• 1873-59-2 4-hydroxy-3-methyl-2-quinolone 
• 55567-59-4 3-phenyliminomethyl-4-hydroxy-2-quinolone 

Relevant articles and documents

Synthesis and colon anticancer activity of some novel thiazole/-2-quinolone derivatives

We direct for the synthesis of 1,6,7-trisubstituted-4-phenylthiazol-2(3H)-ylidene)hydrazono)methyl)quinolin-2-one derivatives by the reaction of corresponding thiosemicarbazone derived by 2-quinolone derivatives with 2-bromoacetophenones in presence of triethylamine at room temperature. The mechanism of the formed products was discussed. The structure of the obtained products was fully characterized using different spectral techniques including infrared (IR), nuclear magnetic resonance (NMR), and mass spectrometry (MS) together with elemental analyses. The new synthesized compounds showed a moderate colon anticancer activity.

Azomethine derivatives as UV light absorbers

The present invention provides a UV light absorber comprising an azomethine compound represented by the formula: [wherein R1 is a hydrogen atom, or a straight- or branched-chain alkyl group having 1 to 4 carbon atoms; and R2 and R3 independently represent a hydrogen atom, a carboxyl group, a halogen atom, an alkoxy group having 1 to 4 carbon atoms, a straight- or branched-chain alkyl group having 1 to 12 carbon atoms or an alkoxycarbonyl group having 2 to 5 carbon atoms] as an active ingredient.