1677-29-8

Basic information

• Product Name: N,N''-BIS-(4-FLUORO-PHENYL)-MALONAMIDE
• Synonyms: N,N'-bis(4-fluorophenyl)propanediamide;N1,N1-Bis(4-fluorophenyl)MalonaMide;PropanediaMide,N1,N3-bis(4-fluorophenyl)-
• CAS NO: 1677-29-8
• Molecular Formula: C₁₅H₁₂F₂N₂O₂
• Molecular Weight: 290.268
• Mol File: 1677-29-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 549.3°Cat760mmHg
• Flash Point: 286°C
• Appearance: /
• Density: 1.392g/cm³
• CAS DataBase Reference: N,N''-BIS-(4-FLUORO-PHENYL)-MALONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N''-BIS-(4-FLUORO-PHENYL)-MALONAMIDE(1677-29-8)
• EPA Substance Registry System: N,N''-BIS-(4-FLUORO-PHENYL)-MALONAMIDE(1677-29-8)

Safety Data

• Hazardous Substances Data: 1677-29-8(Hazardous Substances Data)

Usage

General Description

N,N''-BIS-(4-FLUORO-PHENYL)-MALONAMIDE is a chemical compound with the molecular formula C17H14F2N2O2. It is commonly used as a ligand in various chemical reactions and processes, especially in coordination chemistry. N,N''-BIS-(4-FLUORO-PHENYL)-MALONAMIDE has two 4-fluoro-phenyl groups attached to a malonamide backbone, allowing for complex formation with metal ions and other molecules. N,N''-BIS-(4-FLUORO-PHENYL)-MALONAMIDE is known for its ability to form stable complexes with various metal cations, making it useful in catalysis, extraction, and separation processes. Additionally, the compound has potential applications in pharmaceuticals, materials science, and environmental remediation.

Upstream product

• 371-40-4 4-fluoroaniline 
• 108-59-8 malonic acid dimethyl ester 
• 105-53-3 diethyl malonate 

Downstream Products

• 1677-37-8 6-fluoro-4-hydroxy-1H-quinolin-2-one 
• 1614221-71-4 3,3-dibenzyl-6-fluoro-4-hydroxy-3,4-dihydro-1H-quinolin-2-one 
• 1614221-49-6 3,3-dibenzyl-6-fluoro-1H-quinoline-2,4-dione 
• 1309870-85-6 C₁₅H₉FIN₃O₂ 
• 1309870-84-5 C₁₆H₉F₄N₃O₂ 
• 1309870-83-4 C₁₅H₉ClFN₃O₂ 
• 1309870-81-2 C₁₅H₉BrFN₃O₂ 
• 1309870-80-1 C₁₅H₉ClFN₃O₂ 
• 1234896-95-7 C₁₅H₉FN₄O₄ 
• 1234896-94-6 C₁₆H₉FN₄O₂ 

Relevant articles and documents

Synthesis of symmetrically substituted 3,3-dibenzyl-4-hydroxy-3,4-dihydro- 1H-quinolin-2-ones, as novel quinoline derivatives with antibacterial activity

A novel series of symmetrically substituted 3,3-dibenzyl-4-hydroxy-3,4- dihydro-1H-quinolin-2-ones was synthesized and tested as antimicrobials. The minimum inhibitory concentration (MIC) values of the most active heterocycles were slightly higher than those exhibited by levofloxacin, employed as comparator. Structural factors affecting the activity were explored along three diversification points, including the substituents of the aromatic rings of the 3-benzyl moieties, as well as the functionalization of both, the homocyclic ring of the heterocycle and the quinolonic nitrogen atom. 6-Chloro and 3,3-bis(4′-chlorobenzyl) derivatives showed the lower MIC values. Optimally substituted heterocycles were synthesized, which exhibited enhanced activity.

Synthesis of 6-chloro and 6-fluoro-4-hydroxyl-2-quinolone and their azo disperse dyes

In this study, 6-chloro-4-hydroxy-2-quinolone and 6-flouro-4-hydroxy-2-quinolone were synthesized from corresponding dianilides. These compounds were coupled with some diazotized aromatic amines to give the corresponding azo disperse dyes. The structures