76656-53-6

Basic information

• Product Name: 1,6-Pyrenediamine, N,N,N',N'-tetraphenyl-
• CAS NO: 76656-53-6
• Molecular Formula: C40H28N2
• Molecular Weight: 536.676
• Mol File: 76656-53-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1,6-Pyrenediamine, N,N,N',N'-tetraphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-Pyrenediamine, N,N,N',N'-tetraphenyl-(76656-53-6)
• EPA Substance Registry System: 1,6-Pyrenediamine, N,N,N',N'-tetraphenyl-(76656-53-6)

Safety Data

• Hazardous Substances Data: 76656-53-6(Hazardous Substances Data)

Upstream product

• 129-00-0 pyrene 
• 77-48-5 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione 
• 122-39-4 diphenylamine 
• 27973-29-1 1,6-dibromopyrene 
• 13716-12-6 tri-tert-butyl phosphine 
• 32005-36-0 bis(dibenzylideneacetone)-palladium⁽⁰⁾ 
• 865-48-5 sodium t-butanolate 

Relevant articles and documents

Synthesis of 1,6-disubstituted pyrene-based conjugated microporous polymers for reversible adsorption and fluorescence sensing of iodine

Here we present detailed evidence of highly efficient iodine capture and sensing in 1,6-disubstituted pyrene-based fluorescent conjugated microporous polymers, which were synthesized by a Sonogashira-Hagihara polycondensation reaction (TDP), trimerization

COMPOUND FOR ORGANIC ELECTROLUMINESCENT DEVICE AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

Provided in the present invention are a compound for an organic electroluminescent device and an organic electroluminescent device comprising the same. Accordingly, provided are the organic electroluminescent device used as a dopant of a light emitting la

Synthesis, structural and spectral properties of diarylamino-functionalized pyrene derivatives via Buchwald-Hartwig amination reaction

A new series of diarylamino-functionalized pyrene derivatives, namely, 1-(N,N-diarylamino)-substituted pyrenes (7), isomer of 1,6-bis- and 1,8-bis(N,N-diarylamino)-substituted pyrenes (8/9) and 1,3,6,8-tetrakis(N,N- diarylamino)-substituted pyrenes (10) have been synthesized. The structures of these synthesized compounds were determined on the basis of spectral data and elemental analysis. All compounds 7-10 have bright fluorescent emissions from sky-blue to green in solution condition (λmax = 464-500 nm in CH2Cl2) and high emission efficiency (Φf = 0.84-0.96 in dichloromethane). All compounds have high thermal stability and good solubility in common organic solvents. The electronic properties of these compounds were determined by spectroscopic methods such as UV-vis absorption spectroscopy and fluorescence emission spectroscopy. Clear evidences were obtained that the longest wavelength bands of these compounds are bathochromically red-shifted as the number of the diarylamino-substituent increased.