10537-12-9

Basic information

• Product Name: 9-Phenyl-9,10-dihydroacridine
• Synonyms: 9,10-Dihydro-9-phenylacridine;9-Phenyl-9,10-dihydroacridine;9-Phenylacridan
• CAS NO: 10537-12-9
• Molecular Formula: C₁₉H₁₅N
• Molecular Weight: 257.3291
• Mol File: 10537-12-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 170 °C
• Boiling Point: 389.8°Cat760mmHg
• Flash Point: 200.7°C
• Appearance: /
• Density: 1.137g/cm³
• Vapor Pressure: 2.79E-06mmHg at 25°C
• Refractive Index: 1.64
• PKA: 1.57±0.40(Predicted)
• CAS DataBase Reference: 9-Phenyl-9,10-dihydroacridine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Phenyl-9,10-dihydroacridine(10537-12-9)
• EPA Substance Registry System: 9-Phenyl-9,10-dihydroacridine(10537-12-9)

Safety Data

• Hazardous Substances Data: 10537-12-9(Hazardous Substances Data)

Usage

General Description

9-Phenyl-9,10-dihydroacridine is a chemical compound with a molecular formula C19H15N. It is a polycyclic aromatic hydrocarbon that is used in organic synthesis as a building block for the preparation of various heterocyclic compounds. It is also used as a starting material for the synthesis of pharmaceuticals and agrochemicals. Due to its unique structure, 9-Phenyl-9,10-dihydroacridine exhibits interesting photophysical and electrochemical properties, making it potentially useful in the development of materials for electronic devices and organic light-emitting diodes. However, it is important to handle this compound with caution, as it may pose health hazards if not handled properly.

InChI:InChI=1/C19H15N/c1-2-8-14(9-3-1)19-15-10-4-6-12-17(15)20-18-13-7-5-11-16(18)19/h1-13,19-20H

Upstream product

• 260-94-6 acridine 
• 591-51-5 phenyllithium 
• 602-56-2 9-phenylacridine 
• 408315-87-7 9-(2-iodo-phenyl)-9,10-dihydro-acridine 
• 64-17-5 ethanol 
• 60-29-7 diethyl ether 
• 7647-01-0 hydrogenchloride 
• 88-67-5 2-Iodobenzoic acid 
• 857614-19-8 9-(2-iodo-phenyl)-acridine 
• 122-39-4 diphenylamine 
• 4051-56-3 N,N-diphenylbenzamide 
• 98-07-7 Benzotrichlorid 
• 65-85-0 benzoic acid 

Downstream Products

• 102949-21-3 10-benzyl-9-phenyl-(9,10-dihydroacridine) 
• 56875-26-4 10-methyl-9-phenyl-9,10-dihydroacridine 
• 602-56-2 9-phenylacridine 
• 123607-36-3 10-methyl-9-phenyl-acridinium; chloride-monohydrate 
• 1352136-04-9 4,9-diphenylacridine 
• 1352136-28-7 9-phenyl-4-(2-tolyl)acridine 

Relevant articles and documents

-

-

Selective Catalytic Hydrogenation of Heteroarenes with N-Graphene-Modified Cobalt Nanoparticles (Co3O4-Co/NGratα-Al2O3)

Cobalt oxide/cobalt-based nanoparticles featuring a core-shell structure and nitrogen-doped graphene layers on alumina are obtained by pyrolysis of Co(OAc)2/phenanthroline. The resulting core-shell material (Co3O4-Co/NGratα-Al2O3) was successfully applied in the catalytic hydrogenation of a variety of N-heteroarenes including quinolines, acridines, benzo[h], and 1,5-naphthyridine as well as unprotected indoles. The peculiar structure of the novel heterogeneous catalyst enables activation of molecular hydrogen at comparably low temperature. Both high activity and selectivity were achieved in these hydrogenation processes, to give important building blocks for bioactive compounds as well as the pharmaceutical industry.

Reduction of 9-substituted acridines with nickel-aluminum alloy

9-Methyl-, 9-ethyl-, 9-propyl-, 9-isopropyl-, and 9-phenylacridines were treated with nickel-aluminum alloy in hydrochloric acid to give the corresponding 1,2,3,4,5,6,7,8-octahydroacridines and 9,10-dihydroacridines. The yields are dependent upon the C-9