855004-46-5

Upstream product

• 131-09-9 2-chloroanthracene-9,10-dione 
• 4688-76-0 2-Biphenylboronic acid 

Downstream Products

• 855004-51-2 2-(2-biphenylyl)-9,10-bis(3-(1-naphthyl)phenyl)-9,10-dihydroxy-9,10-dihydroanthracene 
• 855004-47-6 2-(2-biphenylyl)-9,10-bis(3,5-diphenylphenyl)-9,10-dihydroxy-9,10-dihydroanthracene 
• 855004-55-6 2-(2-biphenylyl)-9,10-bis(4-(2,2-diphenylvinyl)phenyl)-9,10-dihydroxy-9,10-dihydroanthracene 
• 855004-53-4 2-(2-biphenylyl)-9,10-bis(4-(1-naphthyl)phenyl)-9,10-dihydroxy-9,10-dihydroanthracene 
• 855004-57-8 2-(2-biphenylyl)-9,10-bis(4-(2-(2,2-diphenylvinyl)phenyl)phenyl)-9,10-dihydroxy-9,10-dihydroanthracene 

Relevant academic research and scientific papers

Method for producing aromatic compound and aromatic compound

A process for producing an aromatic compound which can effectively decrease the contents of halogen elements in the aromatic compound and an aromatic compound which is produced in accordance with the process and useful as the material for obtaining an organic electroluminescence device having a long life are provided. The process for producing an aromatic compound comprises bringing an aromatic compound which is produced via an intermediate compound having halogen elements and has contents of halogen elements of 10 to 1,000 ppm by mass into reaction with a dehalogenating agent to decrease the contents of halogen elements to 10 ppm by mass or smaller, and an aromatic compound which is produced in accordance with the process.

AROMATIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

An aromatic compound represented by a following general formula (1), wherein R1 to R14 each independently represents any one selected from a group consisting of a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group having 1 to 40 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 40 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 40 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 40 carbon atoms, a substituted or unsubstituted aryl group having 6 to 40 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 40 carbon atoms; at least one of R1 to R9 represents a substituted or unsubstituted aryl group having 6 to 40 carbon atoms; and at least one of R10 or R14 represents a substituted or unsubstituted aryl group having 6 to 40 carbon atoms. A compound for obtaining an organic EL device having an enhanced efficiency of light emission and a prolonged half lifetime of brightness is provided.