1417305-21-5

Basic information

• Product Name: 1,1-difluoro-3-phenyl-1H-1λ⁴,11λ⁴-[1,3,2]oxazaborinino[3,4-a]quinoline
• Synonyms: 1,1-difluoro-3-phenyl-1H-1λ⁴,11λ⁴-[1,3,2]oxazaborinino[3,4-a]quinoline
• CAS NO: 1417305-21-5
• Molecular Weight: 295.096
• Mol File: 1417305-21-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,1-difluoro-3-phenyl-1H-1λ⁴,11λ⁴-[1,3,2]oxazaborinino[3,4-a]quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-difluoro-3-phenyl-1H-1λ⁴,11λ⁴-[1,3,2]oxazaborinino[3,4-a]quinoline(1417305-21-5)
• EPA Substance Registry System: 1,1-difluoro-3-phenyl-1H-1λ⁴,11λ⁴-[1,3,2]oxazaborinino[3,4-a]quinoline(1417305-21-5)

Safety Data

• Hazardous Substances Data: 1417305-21-5(Hazardous Substances Data)

Upstream product

• 1613-37-2 Quinoline N-oxide 
• 7338-94-5 1,3-diphenyl-2-propynone 
• 109-63-7 boron trifluoride diethyl etherate 
• 119388-44-2 (Z)-1-phenyl-2-(quinolin-2-yl)ethenol 
• 1531-38-0 2-benzoylmethylquinoline 

Relevant articles and documents

Efficient fluorophores based on pyridyl-enolato and enamido difluoroboron complexes: Simple alternatives to boron-dipyrromethene (bodipy) dyes

Simple [N,O] and [N,N]β-pyridyl or quinolyl enolato/enamido difluoroboron complexes are easily accessible and highly luminescent with good photophysical properties, comparable to BODIPY benchmark dyes. Complete characterization by multinuclear NMR and by

Study on the structureeproperty relationship in a series of novel BF2 chelates with multicolor fluorescence

A series of multicolor fluorescent N,O-bidentate BF2 complexes with variable ligand structures have been synthesized. These complexes exhibit the solvent-independent optical properties and large Stoke shifts. The electrochemical measurements demonstrate that all these chelates are better electron acceptors than the commonly used material Alq3. A qualitative structureeproperty relationship among these complexes has been established on the ground of the experimental data along with the density functional theory (DFT) calculations. The theoretically calculated results are in good agreement with those obtained by the experimental determinations.