146748-12-1

Basic information

• Product Name: 5-phenyl-5,10-dihydroindeno[1,2-b]indole
• Synonyms: 5-phenyl-5,10-dihydroindeno[1,2-b]indole
• CAS NO: 146748-12-1
• Molecular Weight: 281.357
• Mol File: 146748-12-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 5-phenyl-5,10-dihydroindeno[1,2-b]indole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-phenyl-5,10-dihydroindeno[1,2-b]indole(146748-12-1)
• EPA Substance Registry System: 5-phenyl-5,10-dihydroindeno[1,2-b]indole(146748-12-1)

Safety Data

• Hazardous Substances Data: 146748-12-1(Hazardous Substances Data)

Upstream product

• 615-13-4 2-indanone 
• 530-50-7 1,1-Diphenylhydrazine 
• 108-86-1 bromobenzene 
• 591-50-4 iodobenzene 
• 100-63-0 phenylhydrazine 
• 7156-31-2 5,6-Dihydroindeno<2,1-b>indole 

Relevant articles and documents

Synthesis and study of the mutagenic activity of di(indeno[2,1-b]indolyl)- and di(indeno[2,1-b]pyrrolyl)methanes and -dimethylsilanes

Dihetaryldimethylsilanes and dihetarylmethanes containing indeno[2,1-b]indolyl and indeno[2,1-b]pyrrolyl fragments were synthesized. Their mutagenic activity was tested according to Ames with standard test strains Salmonella typhimurium TA 1537, TA 98, and TA 100.

Novel 1,2-dihydroindeno[2,1-b]indole compound and organic electroluminescent device comprising the same

The present invention relates to a novel 1,2-dihydroindeno[2,1-b]indole compound and an organic electroluminescent device comprising the same, wherein an organic electroluminescent device with excellent driving voltage, brightness, long life, etc. can be realized by adapting the 1,2-dihydroindeno[2,1-b]indole compound as a host material inside a phosphorescent light-emitting layer.(AA) Comparative example 1(BB) Example 4(CC) Example 5(DD) Example 6COPYRIGHT KIPO 2017

Nickel-catalyzed C-N crossing coupling reaction: The synthetic method for N-aryl substituted indenoindole

A nickel-based catalyst was employed for the first time in the crossing-coupling of indenoindoles with bromo-/iodoarenes. A simple and practical method was provided for the synthesis of N-aryl substituted indenoindole and the mechanism of this reaction was discussed.