23043-52-9

Basic information

• Product Name: 9-ACETAMIDOACRIDINE
• Synonyms: 9-ACETAMIDOACRIDINE;9-Acetylaminoacridine;N-(9-Acridinyl)acetamide;N-(Acridin-9-yl)acetamide
• CAS NO: 23043-52-9
• Molecular Formula: C₁₅H₁₂N₂O
• Molecular Weight: 236.29
• Mol File: 23043-52-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 519.2°Cat760mmHg
• Flash Point: 267.8°C
• Appearance: /
• Density: 1.284g/cm³
• Vapor Pressure: 6.99E-11mmHg at 25°C
• Refractive Index: 1.741
• CAS DataBase Reference: 9-ACETAMIDOACRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 9-ACETAMIDOACRIDINE(23043-52-9)
• EPA Substance Registry System: 9-ACETAMIDOACRIDINE(23043-52-9)

Safety Data

• Hazardous Substances Data: 23043-52-9(Hazardous Substances Data)

Usage

Safety Profile

Mutation data reported. Whenheated to decomposition it emits toxic vapors of NOx.

InChI:InChI=1/C15H12N2O/c1-10(18)16-15-11-6-2-4-8-13(11)17-14-9-5-3-7-12(14)15/h2-9H,1H3,(H,16,17,18)

Upstream product

• 110166-26-2 aminacrine 
• 108-24-7 acetic anhydride 
• 134-50-9 acridin-9-amine hydrochloride 
• 60-35-5 acetamide 
• 260-94-6 acridine 

Downstream Products

• 578-95-0 10H-acridin-9-one 

Relevant articles and documents

Oxidative SNH amidation of acridine and tautomerism of N-(acridin-9-yl)benzamides

[Figure not available: see fulltext.] Direct oxidative nucleophilic substitution of hydrogen atom in acridine molecule was used to synthesize 9-acylaminoacridines. The prototropic amine-imine tautomerism of these compounds was studied.

Competitive Singlet-Singlet Energy Transfer and Electron Transfer Activation of Aryl Azides: Application to Photo-Cross-Linking Experiments

Direct irradiation of 4-phenyl azide (DAA) in an inert solvent with UV light causes ring expansion to an inermediate dehydroazepine and eventual isolation of 4,4'-azobisbenzene> (AZB).The dehydroazepine can be trapped with nucleophilic reagents to give substituted 3H-azepines.The photochemistry of DAA takes a different course when it is sensitized by pyrene, 1-acetamidopyrene (5), or 9-acetamidoacridine (2).Under these conditions, single-electron transfer occurs in competition with energy transfer as evidenced by detection of radical ions in laser transient absorption spectroscopy and by formation of 4-aniline (DAH) as a major product.Energy transfer and electron transfer compete also when the sensitizer and the aryl azide are linked together by a flexible chain of methylene groups.These results have particular significance for the application of such compounds to phtolabeling experiments.