Maeng, Jee Hyun team published research in Dyes and Pigments in 2021 | 1575-37-7

Computed Properties of 1575-37-7, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., 1575-37-7.

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 1575-37-7, formula is C6H7BrN2, The most pervasive is the naturally produced bromomethane. Computed Properties of 1575-37-7

Maeng, Jee Hyun;Braveenth, Ramanaskanda;Jung, Young Hun;Hwang, Soon Jae;Lee, Hyuna;Min, Hye Li;Kim, Jun Yun;Han, Chang Wook;Kwon, Jang Hyuk research published 《 Efficiency enhancement in orange red thermally activated delayed fluorescence OLEDs by using a rigid di-indolocarbazole donor moiety》, the research content is summarized as follows. The development of orange-red thermally activated delayed fluorescence (TADF) materials with good optoelectronic and electroluminescence properties are full of challenges due to limited mol. designs. Herein, we investigated a series of materials using dimethylacridine (DMAC) and diindolocarbazole (DI) donor with dibenzo [a, c] phenazine (DBP) acceptor, and compared the characteristics of all synthesized materials as emitters. Due to lower singlet energy level, the rate constant of internal conversion (kIC) contribute to nonradiative decay cannot be ignored at the orange-red region. Therefore, employing rigid donor and acceptor moieties play a major role in suppressing kIC. We observed that employing a rigid donor of DI at β position enhanced the PLQY of 96.1% when compared to acridine based emitters. 5-(dibenzo [a, c] phenazin-11-yl)-10, 15-diphenyl-10,15-dihydro-5H-diindolo [3, 2-a:3′, 2′-c] carbazole (β-DI-DBP) based OLED device showed better current efficiency (CEmax) of 47.1 cd/A and maximum external quantum efficiency (EQE) of 23.8%. This work demonstrates a better approach towards high PLQY orange red TADF material development.

Computed Properties of 1575-37-7, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., 1575-37-7.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary