37694-95-4

Basic information

• Product Name: IMidazo[1,2-f]phenanthridine
• Synonyms: IMidazo[1,2-f]phenanthridine
• CAS NO: 37694-95-4
• Molecular Formula: C₁₅H₁₀N₂
• Molecular Weight: 218.2533
• Mol File: 37694-95-4.mol
• Article Data: 12

Chemical Properties

• Melting Point: 140-141℃ (acetone )
• Boiling Point: 382.7±24.0 °C(Predicted)
• Appearance: /
• Density: 1.24±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 6.80±0.30(Predicted)
• CAS DataBase Reference: IMidazo[1,2-f]phenanthridine(CAS DataBase Reference)
• NIST Chemistry Reference: IMidazo[1,2-f]phenanthridine(37694-95-4)
• EPA Substance Registry System: IMidazo[1,2-f]phenanthridine(37694-95-4)

Safety Data

• Hazardous Substances Data: 37694-95-4(Hazardous Substances Data)

Usage

General Description

Imidazo[1,2-f]phenanthridine is a chemical compound that belongs to the class of heterocyclic compounds. It is composed of a fused imidazole and phenanthridine ring system and is used as a building block in the synthesis of various pharmaceuticals and organic compounds. Imidazo[1,2-f]phenanthridine derivatives have also been studied for their potential biological activities, including anticancer, antiviral, and antimicrobial properties. The compound's unique structure and diverse reactivity make it a valuable tool in organic synthesis and medicinal chemistry research.

Upstream product

• 36811-70-8 2,3-dihydro-imidazo[1,2-f]phenanthridine 
• 885107-95-9 C₁₅H₁₄N₂ 
• 229-87-8 phenanthridine 
• 288-32-4 1H-imidazole 
• 2236-52-4 2,2'-diiodobiphenyl 
• 615-43-0 2-iodophenylamine 
• 1309981-07-4 2-cyanophenylboronic acid pinacol ester 
• 107-20-0 2-chloroethanal 
• 832-68-8 6-aminophenanthridine 
• 67-63-0 isopropyl alcohol 
• 670-96-2 2-Phenylimidazole 
• 583-53-9 2,3-dibromobenzene 
• 1015-89-0 6(5H)-phenanthridinone 
• 15679-03-5 6-chlorophenanthridine 

Downstream Products

• 946147-45-1 3-(2,6-dichlorophenyl)imidazo[1,2-f]phenanthridine 
• 946147-46-2 3-(2,6-diphenylphenyl)imidazo[1,2-f]phenanthridine 

Relevant articles and documents

Palladium-catalyzed construction of heteroatom-containing π-conjugated systems by intramolecular oxidative C-H/C-H coupling reaction

Synthesis of heteroatom-containing ladder-type π-conjugated molecules was successfully achieved via a palladium-catalyzed intramolecular oxidative C-H/C-H cross-coupling reaction. This reaction provides a variety of π-conjugated molecules bearing heteroatoms, such as nitrogen, oxygen, phosphorus, and sulfur atoms, and a carbonyl group. The π-conjugated molecules were synthesized efficiently, even in gram scale, and larger π-conjugated molecules were also obtained by a double C-H/C-H cross-coupling reaction and successive oxidative cycloaromatization.

METAL-ASSISTED DELAYED FLUORESCENT EMTTTERS EMPLOYING BENZO-IMIDAZO-PHENANTHRIDINE AND ANALOGUES

Metal-assisted delayed fluorescent emitters employing benzo-imidazo-phenanthridine and analogues for full color displays and lighting applications.

METAL COMPLEXES OF CYCLOMETALLATED IMIDAZO[1,2-f]PHENANTHRIDINE AND DIIMIDAZO[1,2-A:1',2'-C]QUINAZOLINE LIGANDS AND ISOELECTRONIC AND BENZANNULATED ANALOGS THEREOF

The present invention refers to-imidazo [1,2-f] the dee trillion which gets torn phenylphenanthridines and [1,2-a:1 ', 2' -c] quinazoline ligands, or its isoelectronic characteristic and or phosphor including analogue relates to compounds including metal complex. Furthermore, the present invention refers to these compounds including relates organic light emitting diode devices. (by machine translation)