775292-86-9

Basic information

• Product Name: 9-amino-3,3-dimethyl-1,2,3,4-tetrahydroacridin-1-one
• CAS NO: 775292-86-9
• Molecular Weight: 240.305
• Mol File: 775292-86-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 9-amino-3,3-dimethyl-1,2,3,4-tetrahydroacridin-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 9-amino-3,3-dimethyl-1,2,3,4-tetrahydroacridin-1-one(775292-86-9)
• EPA Substance Registry System: 9-amino-3,3-dimethyl-1,2,3,4-tetrahydroacridin-1-one(775292-86-9)

Safety Data

• Hazardous Substances Data: 775292-86-9(Hazardous Substances Data)

Upstream product

• 145657-28-9 N-(5,5-dimethyl-3-oxo-cyclohexen-1-yl)-2-aminobenzonitrile 
• 126-81-8 dimedone 
• 1885-29-6 anthranilic acid nitrile 
• 130187-17-6 2-(5,5-dimethyl-3-oxocyclohexen-1-yl)aminobenzonitrile hydrochloride 
• 7447-39-4 copper(II) chloride 

Downstream Products

• 1179998-41-4 C₂₂H₂₀N₄ 

Relevant articles and documents

Synthesis of 4-methyl-2,3-disubstituted quinoline scaffolds via environmentally benign Fe(iii) catalysed sequential condensation, cyclization and aromatization of 1,3-diketone and 2-ethynylaniline

Environmentally benign Fe(iii)-catalysed sequential condensation, cyclization and aromatization of 1,3-diketone and 2-ethynylaniline derivatives to the substituted quinoline scaffolds with good to excellent yield in shorter reaction time is described. This journal is

Synthesis and crystal structure of 7,8-dihydroquinolino[2,3-a]acridine derivatives

Novel 9-amino-3-substituted-1,2,3,4-acridin-1-one derivatives and 9,14-diamino-7-substituted-7,8-dihydroquinolino[2,3-a]acridine derivatives were synthesized by the condensation reaction of 5-substituted-1,3-cyclohexanedione with 2-aminobenzonitrile and s

DERIVATIVES OF 9-AMINOACRIDINE HAVING PSYCHOTROPIC, ANTIAMNESTIC AND LIPID REGULATING PROPERTIES

New chemical compounds, derivatives of 9-aminoacridine of general formula (I) where R = H, CH3; R1 = H, CH3, Br; R2 = H, CH3; R3 = alkyl-C1-C5, arylmethyl, diethylaminoethyl; X = C = O, CHOH; Y = CH2; X + Y = CH = CH; and their salts with organic and non-organic acids. The desired compounds are obtained by interaction of substituted nitriles of antranyl acid with dimedone with subsequent cyclization of intermediate enaminonitriles into corresponding ketones of 9-aminoacridine after the reduction of which and of their derivatives alkylated or aralkylated on the 9-amino group, the corresponding alcohols are obtained, after hydration of which 9-amino-3,4-dihydroacridines are obtained. When experimented on animals, the said derivatives of 9-aminoacridine have shown psychotropic, antiamnestic and lipid regulating properties, as well as a lower toxicity in comparison with known preparations.