41694-77-3

Basic information

• Product Name: 6-Phenyl-7H-benz[de]anthracen-7-one
• Synonyms: 6-Phenyl-7H-benz[de]anthracen-7-one
• CAS NO: 41694-77-3
• Molecular Formula: C₂₃H₁₄O
• Molecular Weight: 0
• Mol File: 41694-77-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 551.4°C at 760 mmHg
• Flash Point: 245.9°C
• Appearance: /
• Density: 1.254g/cm³
• Vapor Pressure: 3.31E-12mmHg at 25°C
• Refractive Index: 1.719
• CAS DataBase Reference: 6-Phenyl-7H-benz[de]anthracen-7-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Phenyl-7H-benz[de]anthracen-7-one(41694-77-3)
• EPA Substance Registry System: 6-Phenyl-7H-benz[de]anthracen-7-one(41694-77-3)

Safety Data

• Hazardous Substances Data: 41694-77-3(Hazardous Substances Data)

Usage

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

Upstream product

• 41694-76-2 6-Phenyl-6H-benzo[de]anthracen-7-ol 
• 82-05-3 7H-benz[d,e]anthracene-7-one 
• 100-58-3 phenylmagnesium bromide 
• 1623-99-0 phenyl sodium 
• 66003-76-7 Diphenyliodonium triflate 
• 86-55-5 1-naphthalenecarboxylic acid 

Downstream Products

• 860528-23-0 9,10-dioxo-4-phenyl-9,10-dihydro-anthracene-1-carboxylic acid 
• 408337-57-5 4-hydroxy-6-phenyl-benz[de]anthracen-7-one 
• 144-62-7 oxalic acid 

Relevant articles and documents

Spiro compound and application thereof, and organic electroluminescent device and electronic device using same

The invention belongs to the field of organic materials, and relates to a spiro compound and an application thereof, and an organic electroluminescent device and an electronic device using the spiro compound. The spiro compound has a structure represented by a formula 1 shown in the description: wherein the group A has a structure represented by a formula 2; and Ar2 is selected from a group consisting of structures shown as a formula a', a formula b', a formula c' and a formula d'. The spiro compound is used as a hole transport material and is applied to an OLED (Organic Light Emitting Diode)device, and a good device performance and relatively low voltage can be obtained.

Selective introducing of aryl and amino groups: Reaction of benzanthrone and organometallic reagents

The reaction of benzanthrone and aryl magnesium bromides produced 6-aryl-substituted benzanthrones in moderate to good yields. Similarly, 6-alkylaminobenzanthrones were selectively prepared by the reaction of benzanthrone and lithium alkylamides. In contrast, for the lithium arylamides, the arylamino groups were selectively introduced at the 4-position of the benzanthrone.