1217344-01-8

Basic information

• Product Name: 7-{6-bromo-3-[7-(diphenylamino)-9,9-dihexyl-9H-fluoren-2-yl]-quinoxalin-2-yl}-9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine
• Synonyms: 7-{6-bromo-3-[7-(diphenylamino)-9,9-dihexyl-9H-fluoren-2-yl]-quinoxalin-2-yl}-9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine
• CAS NO: 1217344-01-8
• Molecular Weight: 1208.52
• Mol File: 1217344-01-8.mol

Chemical Properties

• CAS DataBase Reference: 7-{6-bromo-3-[7-(diphenylamino)-9,9-dihexyl-9H-fluoren-2-yl]-quinoxalin-2-yl}-9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 7-{6-bromo-3-[7-(diphenylamino)-9,9-dihexyl-9H-fluoren-2-yl]-quinoxalin-2-yl}-9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine(1217344-01-8)
• EPA Substance Registry System: 7-{6-bromo-3-[7-(diphenylamino)-9,9-dihexyl-9H-fluoren-2-yl]-quinoxalin-2-yl}-9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine(1217344-01-8)

Safety Data

• Hazardous Substances Data: 1217344-01-8(Hazardous Substances Data)

Upstream product

• 1217344-00-7 1,2-bis(7-(diphenylamino)-9,9-dihexyl-9H-fluoren-2-yl)ethane-1,2-dione 
• 1575-37-7 4-Bromo-benzene-1,2-diamine 

Downstream Products

• 1616971-42-6 7,7'-{6-[(trimethylsilyl)ethynyl]quinoxaline-2,3-diyl}bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine) 
• 1616971-39-1 7,7'-(6-iodoquinoxaline-2,3-diyl)bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine) 
• 1429808-29-6 7,7'-[6-({2,3-bis[7-(diphenylamino)-9,9-dihexyl-9H-fluoren-2-yl]quinoxalin-6-yl}amino)quinoxaline-2,3-diyl]bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine) 
• 1346520-17-9 7,7'-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline-2,3-diyl)bis(9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine) 
• 1346520-16-8 7-(3-(7-(diphenylamino)-9,9-dihexyl-9H-fluoren-2-yl)-6-vinylquinoxalin-2-yl)-9,9-dihexyl-N,N-diphenyl-9H-fluoren-2-amine 
• 1346520-15-7 C₁₆₆H₁₇₆N₈ 

Relevant articles and documents

Synthesis and two-photon absorption property characterizations of small dendritic chromophores containing functionalized quinoxaliniod heterocycles

A series of star-shaped multi-polar chromophores (compounds 1-3) containing functionalized quinoxaline and quinoxalinoid (indenoquinoxaline and pyridopyrazine) units has been synthesized and characterized for their two-photon absorption (2PA) properties both in the femtosecond and the nanosecond time domain. Under our experimental conditions, these model fluorophores are found to manifest strong and wide-dispersed two-photon absorption in the near-infrared region. It is demonstrated that molecular structures with multi-branched π frameworks incorporating properly functionalized quinoxalinoid units would possess large molecular nonlinear absorptivities within the studied spectral range. Effective optical-power attenuation and stabilization behaviors in the nanosecond time domain of a selected representative dye molecule (i.e., compound 2) from this model compound set were also investigated and the results indicate that such structural motif could be a useful approach for the molecular design toward strong two-photon-absorbing material systems for quick-responsive and broadband optical-suppressing-related applications, particularly to confront long laser pulses. Copyright

Synthesis and two-photon absorption properties of symmetrical chromophores derived from 2,3,5-trisubstituted quinoxaline units

A set of symmetrically substituted multibranched chromophores composed of three quinoxaline-based congeners has been synthesized and experimentally shown to possess strong and widely dispersed two-photon absorptivities in the visible to near-IR region und

Synthesis and two-photon properties of a multi-polar chromophore based on tetra-quinoxalinylethylene scaffold

A new multi-branched fluorophore derived from tetra-quinoxalinylethylene as the core with diphenylaminofluorene units incorporated at the peripheral positions has been synthesized via Pd-catalyzed Suzuki coupling and experimentally shown to possess strong

Two-photon absorption and effective broadband optical power limiting properties of a multi-branched chromophore containing 2,3-diarylquinoxalinyl moieties as the electron-pulling units

A novel multi-branched chromophore containing 2,3-diarylquinoxalinyl units as the electron-acceptors had been synthesized and its nonlinear optical properties were characterized in the femtosecond and nanosecond regime. The experimental results show that the studied fluorophore possesses strong and wide-dispersed two-photon absorption in near infrared (NIR) region. It is demonstrated that the incorporation of 2,3-disubstituted quinoxaline moieties as a part of π-conjugation in a dye molecule could be a useful approach toward large molecular two-photon absoptivities within the studied spectral region. Effective optical-power-attenuation behaviors in the nanosecond time domain of this compound were also investigated and the results indicate that such dye molecule can be a potential material as a broadband and quick-responsive optical limiter especially when against those laser lights with longer pulses.