1310727-09-3

Basic information

• Product Name: 2,7-bis(4-tert-octylphenylethynyl)-9,10-dimethoxyphenanthrene
• Synonyms: 2,7-bis(4-tert-octylphenylethynyl)-9,10-dimethoxyphenanthrene
• CAS NO: 1310727-09-3
• Molecular Weight: 662.956
• Mol File: 1310727-09-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,7-bis(4-tert-octylphenylethynyl)-9,10-dimethoxyphenanthrene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,7-bis(4-tert-octylphenylethynyl)-9,10-dimethoxyphenanthrene(1310727-09-3)
• EPA Substance Registry System: 2,7-bis(4-tert-octylphenylethynyl)-9,10-dimethoxyphenanthrene(1310727-09-3)

Safety Data

• Hazardous Substances Data: 1310727-09-3(Hazardous Substances Data)

Upstream product

• 849907-81-9 4-tert-octyl-1-trifluoromethanesulfonyloxybenzene 
• 84-11-7 9,10-phenanthrenequinone 
• 140-66-9 tert-octylphenol 
• 16218-32-9 2,7-diiodophenanthrene-9,10-quinone 
• 1334015-13-2 2-methyl-4-(4-tert-octylphenyl)-but-3-yn-2-ol 
• 1310727-03-7 2,7-diiodo-9,10-dimethoxyphenanthrene 
• 849907-82-0 1-ethynyl-4-(1,1,3,3-tetramethylbutyl)benzene 

Downstream Products

• 1310727-17-3 2,7-bis(4-tert-octylphenylethynyl)-phenanthrene-9,10-dione 

Relevant articles and documents

Synthesis and photophysics of dibenz[a,c]phenazine derivatives

The synthesis of dipolar dibenz[a,c]phenazine (DBP) derivatives is described. The compounds possess little electronic communication between donor and acceptor units in the ground state regardless of the pattern of substitution. The dipolar derivatives deactivate mostly via electron transfer (eT) under polar conditions. Intersystem crossing is likely to compete for S1 relaxation.