116690-69-8

Basic information

• Product Name: Acridine, 7-chloro-1,2,3,4-tetrahydro-9-phenyl-
• CAS NO: 116690-69-8
• Molecular Formula: C19H16ClN
• Molecular Weight: 293.796
• Mol File: 116690-69-8.mol
• Article Data: 65

Chemical Properties

• CAS DataBase Reference: Acridine, 7-chloro-1,2,3,4-tetrahydro-9-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Acridine, 7-chloro-1,2,3,4-tetrahydro-9-phenyl-(116690-69-8)
• EPA Substance Registry System: Acridine, 7-chloro-1,2,3,4-tetrahydro-9-phenyl-(116690-69-8)

Safety Data

• Hazardous Substances Data: 116690-69-8(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 719-59-5 5-chloro-2-aminobenzophenone 
• 108-93-0 cyclohexanol 
• 636-82-8 cyclohexene-1-carboxylic acid 
• 719-64-2 5-chloro-3-phenylanthranil 
• 144930-52-9 (4-chlorophenyl)(phenyl)iodonium triflate 
• 111-24-0 1,5-dibromo-pentane 
• 536-74-3 phenylacetylene 
• 92078-65-4 (7-bromohept-1-yn-1-yl)benzene 
• 113106-05-1 7-chloro-1,2,3 ,4-tetrahydroacridin-9-(10H)-one 
• 1629174-85-1 7-chloro-1,2,3,4-tetrahydroacridin-9-yl trifluoromethanesulfonate 
• 98-80-6 phenylboronic acid 
• 591-50-4 iodobenzene 
• 15295-69-9 hept-6-ynenitrile 

Relevant articles and documents

Friedlaender synthesis of poly-substituted quinolines in the presence of triethylammonium hydrogen sulfate [Et3NH][HSO4] as a highly efficient, and cost effective acidic ionic liquid catalyst

A rapid and an efficient method for the preparation of a variety of substituted quinolines has been developed through the reactions of o-aminoarylketones with carbonyl compounds containing a reactive α-methylene moiety in the presence of molten [Et3

Synthesis of quinolines via Friedlaender reaction catalyzed by CuBTC metal-organic-framework

Friedlaender condensation between 2-aminoaryl ketones and different carbonyl compounds, catalyzed by CuBTC was investigated by a combination of various experimental techniques and by density functional theory based modelling. CuBTC exhibiting hard Lewis a

Rh-Catalyzed C-H Amination/Annulation of Acrylic Acids and Anthranils by Using -COOH as a Deciduous Directing Group: An Access to Diverse Quinolines

A method for the synthesis of diverse polysubstituted quinolines from readily available acrylic acids and anthranils has been developed. The weakly coordinating -COOH directing group, which can be tracelessly removed in the cascade cyclization, is essential for this reaction. Diverse polysubstituted quinolines were obtained under mild reaction conditions with simple H2O and CO2 as byproducts. More importantly, 1,2,3,4-tetrahydroacridine, which is the core skeleton of tacrine (an Alzheimer's disease drug), was conveniently synthesized.

Sulfated Polyborate Catalyzed Selective Friedlander Annulation for Synthesis of Highly Functionalized Quinolines

-

ZnCl2 supported on Fe3O4@SiO2 core–shell nanocatalyst for the synthesis of quinolines via Friedl?nder synthesis under solvent-free condition

A magnetic nanocatalyst of Fe3O4@SiO2/ZnCl2 was prepared by supporting ZnCl2 on silica-coated magnetic nanoparticles of Fe3O4. This recoverable catalyst was used for the synthesi