61736-68-3

Basic information

• Product Name: 3-methoxyacridin-9-one
• Synonyms: 3-methoxyacridin-9-one
• CAS NO: 61736-68-3
• Molecular Formula: C₁₄H₁₁NO₂
• Molecular Weight: 225.2426
• Mol File: 61736-68-3.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 403.2°Cat760mmHg
• Flash Point: 197.6°C
• Appearance: /
• Density: 1.233g/cm³
• Vapor Pressure: 1.04E-06mmHg at 25°C
• Refractive Index: 1.617
• CAS DataBase Reference: 3-methoxyacridin-9-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methoxyacridin-9-one(61736-68-3)
• EPA Substance Registry System: 3-methoxyacridin-9-one(61736-68-3)

Safety Data

• Hazardous Substances Data: 61736-68-3(Hazardous Substances Data)

Usage

Chemical class

Acridine derivative

Substituent

Methoxy group at 3-position of acridine ring

Uses

Organic synthesis, fluorescent dye, optoelectronic materials

Biological activity

Antibacterial, antifungal properties

Potential application

Development of new antimicrobial agents

InChI:InChI=1/C14H11NO2/c1-17-9-6-7-11-13(8-9)15-12-5-3-2-4-10(12)14(11)16/h2-8H,1H3,(H,15,16)

Upstream product

• 22996-21-0 4-methoxy-2-nitro-benzaldehyde 
• 98-80-6 phenylboronic acid 
• 536-90-3 m-Anisidine 
• 118-91-2 ortho-chlorobenzoic acid 
• 445-29-4 o-fluoro-benzoic acid 
• 27693-73-8 N-(3-methoxyphenyl)anthranilic acid 
• 54788-38-4 2-chloro-4-methoxy-1-methylbenzene 
• 62-53-3 aniline 
• 21971-21-1 2-chloro-4-methoxybenzoic acid 
• 118-92-3 anthranilic acid 
• 36192-61-7 2-amino-4'-methoxybenzophenone 
• 37892-45-8 2-azido-4'-methoxy-benzophenone 
• 525-76-8 2-methyl-4-oxo-3,1-benzoxazine 
• 37892-51-6 3-(4-methoxyphenyl)benzo[c]isoxazole 

Relevant articles and documents

Access to acridones by tandem copper(i)-catalyzed electrophilic amination/Ag(i)-mediated oxidative annulation of anthranils with arylboronic acids

An efficient and practical approach for the synthesis of medicinally important acridones was developed from anthranils and commercially available arylboronic acids by a tandem copper(i)-catalyzed electrophilic amination/Ag(i)-mediated oxidative annulation strategy. This new and straightforward protocol displayed a broad substrate scope (25 examples) and high functional group tolerance. What's more, a possible mechanistic proposal was also presented.

Transition-Metal-Free Synthesis of Acridones via Base-Mediated Intramolecular Oxidative C?H Amination

Intramolecular oxidative C?H amination of 2-aminobenzophenones was achieved in the presence of potassium tert-butoxide and dimethyl sulfoxide. A series of functionalized acridones were prepared in moderate to excellent yields in a mild, efficient, and transition-metal-free manner. (Figure presented.).

Acridone-benzimidazole ring-fused ligands: A new class of sensitizers of lanthanide luminescence via low-energy excitation

Two monotopic tridentate ligands, namely HLAB1 and HL AB2 have been synthesized which feature an acridone chromophore fused on a benzimidazolepyridine framework. They differ from each other by their connection points between a N-meth