| Company Name: |
Beijing HwrkChemical Technology Co., Ltd
|
| Tel: |
010-89508211 18501085097 |
| Email: |
sales.bj@hwrkchemical.com |
| Products Intro: |
Product Name:3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97%
CAS:1987900-95-7
Purity:95.00% Package:100mg
|
| Company Name: |
BeiJing Hwrk Chemicals Limted
|
| Tel: |
0757-86329057 18934348241 |
| Email: |
sales4.gd@hwrkchemical.com |
| Products Intro: |
Product Name:3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97%
CAS:1987900-95-7
Purity:95.00% Package:100mg
|
| Company Name: |
Sigma-Aldrich
|
| Tel: |
021-61415566 800-8193336 |
| Email: |
orderCN@merckgroup.com |
| Products Intro: |
Product Name:3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine
CAS:1987900-95-7
Purity:>=97% Package:100MG Remarks:901111-100MG
|
|
| | 3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97% Basic information |
| Product Name: | 3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97% | | Synonyms: | 3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97%;3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine;3,7-Di([1,1'-biphenyl]-4-yl)-10-(naphthalen-1-yl)-10H-phenoxazine;10H-Phenoxazine, 3,7-bis([1,1'-biphenyl]-4-yl)-10-(1-naphthalenyl)-;Phenox O-PC? A0202;3,7-Di([1,1'-biphenyl]-4-yl)-10-(naphthalen-1-yl)-10H-phenoxazine | | CAS: | 1987900-95-7 | | MF: | C46H31NO | | MW: | 613.74 | | EINECS: | | | Product Categories: | | | Mol File: | 1987900-95-7.mol |  |
| | 3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97% Chemical Properties |
| Melting point | 171°C | | density | 1.209±0.06 g/cm3(Predicted) | | form | powder or crystals | | pka | -0.29±0.20(Predicted) |
| | 3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97% Usage And Synthesis |
| Uses | This phenoxazine-based organic photoredox catalyst (in addition to the dihydrophenazine catalyst 901112) was designed to be a strong excited-state reductant and possesses advanced photophysical and electrochemical properties, enabling it to serve as a sustainable replacement for ruthenium- or iridium-based photoredox catalysts. For example, dihydrophenazine and phenoxazine derivatives were demonstrated to replace ruthenium or iridium complexes in the application of photoredox-catalyzed atom transfer radical polymerization (ATRP) for controlled polymer synthesis and small molecule transformations such as trifluoromethylation, atom transfer radical addition, and dual Nickel/photoredox catalyzed C-N and C-S cross-couplings. Dihydrophenazine- and phenoxazine-based organic photoredox catalysts were introduced in collaboration with the Miyake Research Group. |
| | 3,7-Di(4-biphenyl) 1-naphthalene-10-phenoxazine >=97% Preparation Products And Raw materials |
|