22575-89-9

Basic information

• Product Name: 9-phenyl-1,2,3,4,5,6,7,8-octahydro-acridine
• Synonyms: 9-phenyl-1,2,3,4,5,6,7,8-octahydro-acridine
• CAS NO: 22575-89-9
• Molecular Weight: 263.382
• Mol File: 22575-89-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 9-phenyl-1,2,3,4,5,6,7,8-octahydro-acridine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-phenyl-1,2,3,4,5,6,7,8-octahydro-acridine(22575-89-9)
• EPA Substance Registry System: 9-phenyl-1,2,3,4,5,6,7,8-octahydro-acridine(22575-89-9)

Safety Data

• Hazardous Substances Data: 22575-89-9(Hazardous Substances Data)

Upstream product

• 602-56-2 9-phenylacridine 
• 105772-43-8 phenylhydrazone of 8-R-phenyltricyclo(7.3.1.0^2,7)tridecan-2-ol-13-one 
• 5682-83-7 (E)-2-benzylidenecyclohexanone 
• 15595-71-8 2-aminocyclohex-1-enecarbonitrile 

Relevant articles and documents

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

SYNTHESIS OF HETEROCYCLES FROM 1,5-DIKETONES: 3.* ALICYCLIC 1,5-DIKETONES IN REACTION WITH PHENYLHYDRAZINE

8-R-7aH-5,6,7,8,9,10,11,12-Octahydroindoloacridines, 1,2,3,4-tetrahydrocarbazole,9-R-sym-octahydroacridines, and 9-R,10-phenyl-sym-octahydroacridinium salts are formed by the action of phenyl-hydrazine on alkylidene-2,2'-dicyclohexanine or the corresponding 8-R-tricyclo(7.3.1.02,7)tridecan-2-ol-13-ones in an acid medium.Postulations were made for the paths of formation of these compounds. 2,2-Dimethyl-3-oxa-4a-(2',2'-dimethyltetrahydropyran-4'-on-5'yl-methyl)4aH-1,2,3,4-tetrahydrocarbazole, 3,3,14,14-tetramethyl-2-oxa-5a,10b-(methanoxyisobutane)-1,2,3,4,5a,10b,11,11a-octahydroquinindoline, 2,2-dimethyl-3-oxa-1,2,3,4-tetrahydrocarbazole and 3,3,6,6-tetramethyl-2,7-dioxa-sym-octahydroacridine were obtained by the reaction of methylene-3,3'-di(6,6-dimethyltetrahydropyran-4-one)with phenylhydrazine in acetic acid.The quinindoline structure was confirmed by the synthesis of this compound from 2,2-dimethyl-3-oxa-4a-(2',2'-dimethyltetrahydropyran-4'-on-5'-ylmethyl)-4aH-1,2,3,4-tetrahydrocarbazole by the action of ammonia.