The Chemistry of Heterocyclic Compounds, Volume 9Interscience Publishers, 1956 - Heterocyclic compounds |
Contents
Nomenclature and Numbering System | 1 |
acridines 99 | 9 |
Aminoacridines | 79 |
Copyright | |
10 other sections not shown
Other editions - View all
Common terms and phrases
10-methylacridinium 10-methylacridone 2-Chloro-4-nitrobenzoic acid 2-Chlorobenzoic acid 3-nitroaniline 3,6-diaminoacridine 6-Chloro-2-methoxy 9-amino 9-aminoacridine 9-chloroacridine 9-methylacridine a]acridine Abstracts acetic acridine acridinium salts Acriflavine acronycine Albert alcoholic aldehyde alkali alkaloids amines amino group aniline anthranilic acid antibacterial antimalarial Atebrin atom benz benzene boiling Brit bromine carbonate carboxylic Chapter Chem chim chloride CO₂H colorless compound condensed corresponding cyclisation demethylation derivatives diphenylamine diphenylamine-2-carboxylic acid Drozdov dyes ethanol ether EtOH Exptl fluorescence formed give Graebe H₂N H₂SO4 heating hydrochloric acid hydrogen hydrolysis iodide isolated isomers Lehmstedt Linnell m-phenylenediamine Melicopidine melicopine method methoxy methyl mixture NH₂ nitric acid nitro obtained OMe OMe orange oxidation Pharm Pharmacol phenol phosphorus oxychloride POCI position potassium prakt prepared presence Proflavine properties pyridine quinone reacted reaction reagent reduction ring similar sodium hydroxide soluble solution solvent structure substituents sulphuric acid synthesis Table Ullmann Yellow needles ex yield zinc zinc chloride