69544-85-0

Basic information

• Product Name: 10-(3-nitrobenzylidene)anthracen-9(10H)-one
• Synonyms: 9(10H)-anthracenone, 10-[(3-nitrophenyl)methylene]-
• CAS NO: 69544-85-0
• Molecular Formula: C₂₁H₁₃NO₃
• Molecular Weight: 327.3328
• Mol File: 69544-85-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 496.6°C at 760 mmHg
• Flash Point: 232°C
• Density: 1.351g/cm³
• Vapor Pressure: 5.32E-10mmHg at 25°C
• Refractive Index: 1.72
• CAS DataBase Reference: 10-(3-nitrobenzylidene)anthracen-9(10H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 10-(3-nitrobenzylidene)anthracen-9(10H)-one(69544-85-0)
• EPA Substance Registry System: 10-(3-nitrobenzylidene)anthracen-9(10H)-one(69544-85-0)

Safety Data

• Hazardous Substances Data: 69544-85-0(Hazardous Substances Data)

Usage

Class

Anthraquinones

Applications

Organic synthesis, production of dyes and pigments, photochemistry, and photophysics

Physical state

Yellow to orange crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Photochemical properties

Can undergo photochemical reactions, making it a photoresponsive material

Importance

Wide range of applications in chemical and material science, valuable for researchers and chemists in various industries

Upstream product

• 529-86-2 9-anthrol 
• 99-61-6 3-nitro-benzaldehyde 
• 90-44-8 anthracen-9(10H)-one 

Relevant articles and documents

An expedient regio- and diastereoselective synthesis of hybrid frameworks with embedded spiro[9,10]dihydroanthracene [9,3']-pyrrolidine and Spiro[oxindole-3,2'-pyrrolidine] motifs via an ionic liquid-mediated multicomponent reaction

A series of hitherto unreported anthracene-embedded dispirooxindoles has been synthesized via a one-pot three-component 1,3-dipolar cycloaddition reaction of an azomethine ylide, generated in situ from the reaction of isatin and sarcosine to 10-benzyliden

A facile synthesis of 10-arylmethylene anthracenones under microwave irradiation

10-Arylmethylene anthracenones were synthesised by the condensation of aromatic aldehydes with anthracenone using sodium hydroxide as catalyst under microwave irradiation in good yields.