40239-75-6

Basic information

• Product Name: 1-nitroacridin-9(10H)-one
• CAS NO: 40239-75-6
• Molecular Formula: C₁₃H₈N₂O₃
• Molecular Weight: 240.2142
• Mol File: 40239-75-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 430.9°C at 760 mmHg
• Flash Point: 214.4°C
• Density: 1.409g/cm³
• Vapor Pressure: 1.25E-07mmHg at 25°C
• Refractive Index: 1.672
• CAS DataBase Reference: 1-nitroacridin-9(10H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-nitroacridin-9(10H)-one(40239-75-6)
• EPA Substance Registry System: 1-nitroacridin-9(10H)-one(40239-75-6)

Safety Data

• Hazardous Substances Data: 40239-75-6(Hazardous Substances Data)

Usage

Chemical Family

Acridine
1-nitroacridin-9(10H)-one belongs to the acridine family of compounds.

Derivative

Acridine with a nitro group
It is a derivative of acridine, with a nitro group attached to the 1-position of the molecule.

Potential Applications

Pharmaceuticals, dyes, and pesticides
The compound has potential applications in various fields, including pharmaceuticals, dyes, and pesticides.
4. Cytotoxic and Antitumor Properties
1-nitroacridin-9(10H)-one is known for its cytotoxic and antitumor properties, making it a potential candidate for anticancer drug development.
5. Fluorescent Properties
The compound exhibits fluorescent properties, which makes it useful in the field of fluorescence microscopy and organic light-emitting diodes.
6. Health and Environmental Risks
Despite its potential benefits, 1-nitroacridin-9(10H)-one poses health and environmental risks and should be handled with caution.

Upstream product

• 99-09-2 3-nitro-aniline 
• 88-65-3 2-bromobenzoic-acid 
• 260-94-6 acridine 
• 687978-73-0 6-acetylamino-1-nitro-9-(3-dimethylaminopropylamino)-acridine 
• 86026-78-0 6-acetylamino-1-nitro-9-pyridinium chloride 
• 86026-76-8 potassium 2-bromo-4-acetylaminobenzoate 
• 86026-75-7 N(3'-nitrophenyl)-4-acetylaminoanthranilic acid 
• 86602-06-4 2-(1-Nitro-acridin-9-ylamino)-propionic acid ethyl ester 
• 86602-11-1 N(1-nitroacridyl-9)-DL-asparagine 
• 86602-09-7 3-Hydroxy-2-(1-nitro-acridin-9-ylamino)-butyric acid ethyl ester 
• 86602-07-5 3-Methylsulfanyl-2-(1-nitro-acridin-9-ylamino)-propionic acid ethyl ester 
• 86602-08-6 2-(1-Nitro-acridin-9-ylamino)-propionic acid 
• 81483-74-1 3-(1-Nitro-acridin-9-ylamino)-propionic acid 
• 4533-39-5 nitracrine 

Downstream Products

• 66073-40-3 1-aminoacridin-9(10H)-one 
• 65782-80-1 1-hydroxylamino-9-acridone 
• 72567-64-7 1-amino-2,4-dipiperidinoacridone 
• 7251-00-5 2-nitroacridone 
• 776299-26-4 1-(p-acetylaminobenzenesulphonylamino)-acridone 
• 676456-12-5 1-(p-aminobenzenesulphonylamino)acridone 
• 17431-90-2 1-nitro-9-chloroacridine 
• 578-06-3 acridin-1-ylamine 

Relevant articles and documents

Potent acetylcholinesterase inhibitors: Synthesis, biological assay and docking study of nitro acridone derivatives

The reaction of o-halobenzoic acid with aniline derivatives and their subsequent cyclization reaction yielded the acridone derivatives. The series of nitro acridone derivatives were prepared by Ullmann condensation in presence of copper as catalyst and we

RESEARCH ON TUMOR INHIBITING COMPOUNDS. PART LXVIII. SYNTHESIS OF 1-NITRO-6-ACETYLAMINO-9-AMINOACRIDINE DERIVATIVES.

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