18792-80-8

Basic information

• Product Name: 3-Phenyl-7H-benz[de]anthracen-7-one
• Synonyms: 3-Phenyl-7H-benz[de]anthracen-7-one
• CAS NO: 18792-80-8
• Molecular Formula: C₂₃H₁₄O
• Molecular Weight: 0
• Mol File: 18792-80-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 515°C at 760 mmHg
• Flash Point: 228.8°C
• Appearance: /
• Density: 1.254g/cm³
• Vapor Pressure: 1.02E-10mmHg at 25°C
• Refractive Index: 1.719
• CAS DataBase Reference: 3-Phenyl-7H-benz[de]anthracen-7-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Phenyl-7H-benz[de]anthracen-7-one(18792-80-8)
• EPA Substance Registry System: 3-Phenyl-7H-benz[de]anthracen-7-one(18792-80-8)

Safety Data

• Hazardous Substances Data: 18792-80-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C23H14O/c24-23-20-10-5-4-9-17(20)19-14-13-16(15-7-2-1-3-8-15)18-11-6-12-21(23)22(18)19/h1-14H

Upstream product

• 100-42-5 styrene 
• 50-00-0 formaldehyd 
• 90-44-8 anthracen-9(10H)-one 
• 4159-04-0 10-Methylene-10H-anthracen-9-one 
• 936-59-4 3-chloropropiophenone 
• 140-10-3 (E)-3-phenylacrylic acid 
• 98-95-3 nitrobenzene 
• 14371-10-9 (E)-3-phenylpropenal 
• 90-13-1 1-Chloronaphthalene 
• 52236-54-1 10-cinnamyliden-anthrone 
• 642-31-9 9-anthracene aldehyde 
• 536-74-3 phenylacetylene 
• 7664-93-9 sulfuric acid 
• 211059-29-9 10-(3-oxo-3-phenylpropyl)-9-(10H)-anthracenone 

Downstream Products

• 866997-52-6 4-benzoyl-9,10-dioxo-9,10-dihydro-anthracene-1-carboxylic acid 
• 61726-79-2 1-benzoylanthraquinone 
• 18792-79-5 2-phenyl-benz[de]anthracen-7-one 
• 502187-63-5 6-ethyl-3-phenyl-benz[de]anthracen-7-one 
• 860603-96-9 6-hexyl-3-phenyl-benz[de]anthracen-7-one 

Relevant articles and documents

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Radical Alkyne peri-Annulation Reactions for the Synthesis of Functionalized Phenalenes, Benzanthrenes, and Olympicene

Radical cyclization reactions at a peri position were used for the synthesis of polyaromatic compounds. Depending on the choice of reaction conditions and substrate, this flexible approach led to Bu3Sn-substituted phenalene, benzanthrene, and olympicene derivatives. Subsequent reactions with electrophiles provided synthetic access to previously inaccessible functionalized polyaromatic compounds.