Steinberger, Simon et al. published their research in Chemical Communications (Cambridge, United Kingdom) in 2011 | CAS: 189230-41-9

2-Bromopyridine-3,4-diamine (cas: 189230-41-9) belongs to pyridine derivatives. In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. Halopyridines are particularly attractive synthetic building blocks in a variety of cross-coupling methods, including the Suzuki-Miyaura cross-coupling reaction.Recommanded Product: 2-Bromopyridine-3,4-diamine

Vacuum-processed small molecule solar cells based on terminal acceptor-substituted low-band gap oligothiophenes was written by Steinberger, Simon;Mishra, Amaresh;Reinold, Egon;Levichkov, Jordan;Uhrich, Christian;Pfeiffer, Martin;Baeuerle, Peter. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2011.Recommanded Product: 2-Bromopyridine-3,4-diamine This article mentions the following:

Novel acceptor-donor-acceptor (A-D-A) type oligothiophenes incorporating benzothiadiazole (BTDA) and thiadiazolopyridine (TDAPy) as terminal acceptor groups have been developed for small mol. organic solar cells. In vacuum-processed planar heterojunction solar cells the TDAPy-based oligomer showed a power conversion efficiency of 3.15% and a high fill factor of 0.67. In the experiment, the researchers used many compounds, for example, 2-Bromopyridine-3,4-diamine (cas: 189230-41-9Recommanded Product: 2-Bromopyridine-3,4-diamine).

2-Bromopyridine-3,4-diamine (cas: 189230-41-9) belongs to pyridine derivatives. In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. Halopyridines are particularly attractive synthetic building blocks in a variety of cross-coupling methods, including the Suzuki-Miyaura cross-coupling reaction.Recommanded Product: 2-Bromopyridine-3,4-diamine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem