25379-15-1

Usage

InChI:InChI=1/C15H13NO3/c1-18-11-7-8-12(19-2)14-13(11)15(17)9-5-3-4-6-10(9)16-14/h3-8H,1-2H3,(H,16,17)

Upstream product

• 21193-41-9 9-chloro-1,4-dimethoxyacridine 
• 21193-37-3 2-[(2,5-dimethoxyphenyl)amino]benzoic acid 
• 25245-34-5 1-bromo-2,5-dimethoxybenzene 
• 130399-61-0 ethyl N-(trimethylsilyl)anthranilate 
• 102-56-7 2,5-dimethoxyaniline 
• 88-65-3 2-bromobenzoic-acid 
• 118-91-2 ortho-chlorobenzoic acid 
• 16463-38-0 potassium 2-chlorobenzoate 
• 87-25-2 2-ethoxycarbonylaniline 

Downstream Products

• 141992-59-8 10-(2-Diethylamino-ethyl)-1-hydroxy-4-methoxy-10H-acridin-9-one 
• 141992-60-1 [2-(1,4-Dimethoxy-acridin-9-ylsulfanyl)-ethyl]-diethyl-amine 
• 141992-48-5 9-Ethylsulfanyl-1,4-dimethoxy-acridine 
• 141992-44-1 10-(2-Diethylamino-ethyl)-1,4-dihydroxy-10H-acridin-9-one 
• 141992-47-4 NSC 625987 
• 141992-57-6 10-(2-Dimethylamino-ethyl)-1,4-dimethoxy-10H-acridin-9-one 
• 141992-56-5 10-Ethyl-1,4-dimethoxy-10H-acridin-9-one 

Relevant academic research and scientific papers

Syntheses of 7H-pyrido- and 7H-pyrano[2,3,4-kl]acridin-2(3H)-ones from 9-chloroacridines

A method for peri-annulation of the pyridine or pyran ring to acridine was developed and used to obtain 7H-pyrido-and 7H-pyrano[2,3,4-kl]acridin-2(3H)- ones. The peri-groups were formed by a reaction of 9-chloro-1-nitroacridine with a CH-acid (malononitri

Synthesis of acridine-quinone systems - A potential electrochemical fluorescent switch

The synthesis of various acridine-quinones is reported. The fluorescence-quenching quinone moiety has been incorporated into various acridine molecules, each having a different functionality at the ninth position of the acridine ring. It is envisaged that

Synthesis of ascididemine and an isomer

Ascididemine (9H-quino[4,3,2-de][1,10]phenanthrolin-9-one) (1) and an isomer (9H-quino[4,3,2-de][1,7]phenanthrolin-9-one) (4) have been synthesized starting from 1,4-dimethoxyacridone (7). The acridone was converted into 1,4- dimethoxy-9-ethynylacridine (

Synthesis of benzacridine and pyridoacridine via Diels-Alder reaction of acridonequinone

Synthesis of benz[b]acridones (8) and pyrido[3,2-b]acridones (15) was achieved by Diels-Alder reaction of acridonequinones (5) with several activated 1,3-dienes. The addition proceeded in a regioselective manner under mild conditions, thus providing a con

Structure-trypanodical activity relationships

A set of 9-thioalkylacridinones, has been prepared and investigated' in vitro' against T. cruzi. Structure-antiparasitic activity relationships are detailed with a view to identify the major structural parameters for the activity under consideration.

Use of N-lithiated ethyl anthranilates as 1,4-dipole equivalents in 1,4-dipole-aryne cycloaddition: a novel approach to the synthesis of acridones

A new strategy for acridones based on 1,4-dipolar cycloaddition of N-lithiated ethyl anthranilates, which function as 1,4-dipole equivalents, with arynes is reported.