Li, Xuejing’s team published research in Chemistry – A European Journal in 2019 | 2725-82-8

Chemistry – A European Journal published new progress about Aromatic compounds Role: RCT (Reactant), RACT (Reactant or Reagent). 2725-82-8 belongs to class bromides-buliding-blocks, and the molecular formula is C8H9Br, Application of C8H9Br.

Li, Xuejing; Deng, Xingwang; Coyne, Anthony G.; Srinivasan, Rajavel published the artcile< meta-Nitration of Arenes Bearing ortho/para Directing Group(s) Using C-H Borylation>, Application of C8H9Br, the main research area is meta nitroarene regioselective preparation; arene borylation nitration tandem iridium catalyst copper; C−H borylation; copper catalysis; nitration; nitro(hetero)arenes; one-pot reactions.

The meta-nitration of arenes bearing ortho/para directing group(s) using the iridium-catalyzed C-H borylation reaction followed by a newly developed copper(II)-catalyzed transformation of the crude aryl pinacol boronate esters into the corresponding nitroarenes RNO2 [R = 4,5-di-ClC6H3, 3,4-di-BrC6H3, 5-Cl-3-pyridyl, etc.] in a one-pot fashion was reported. The reaction tolerated a wide array of ortho/para-directing groups, such as -F, -Cl, -Br, -CH3, -Et, -iPr -OCH3 and -OCF3. It also provided regioselective access to the nitro derivatives of π-electron-deficient heterocycles, such as pyridine and quinoline derivatives The application of this method was demonstrated in the late-stage modification of complex mols. and also in the gram-scale preparation of an intermediate en route to the FDA-approved drug Nilotinib. Finally, showed that the nitro product obtained by this strategy could also be directly converted to the aniline or hindered amine through Baran’s amination protocol.

Chemistry – A European Journal published new progress about Aromatic compounds Role: RCT (Reactant), RACT (Reactant or Reagent). 2725-82-8 belongs to class bromides-buliding-blocks, and the molecular formula is C8H9Br, Application of C8H9Br.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Marvi, Omid’s team published research in Bulletin of the Korean Chemical Society in 2009-12-20 | 82-73-5

Bulletin of the Korean Chemical Society published new progress about Microwave irradiation. 82-73-5 belongs to class bromides-buliding-blocks, and the molecular formula is C8H3BrO3, Related Products of 82-73-5.

Marvi, Omid; Giahi, Masoud published the artcile< Montmorillonite KSF clay as novel and recyclable heterogeneous catalyst for the microwave mediated synthesis of indan-1,3-diones>, Related Products of 82-73-5, the main research area is montmorillonite clay catalyst microwave irradiation indan dione synthesis.

Various indan-1,3-dione derivatives were synthesized from the reaction of different phthalic anhydrides with diethyl-malonate using montmorillonite KSF clay as a recyclable heterogeneous acidic catalyst and microwave irradiation in good yields and short reaction times.

Bulletin of the Korean Chemical Society published new progress about Microwave irradiation. 82-73-5 belongs to class bromides-buliding-blocks, and the molecular formula is C8H3BrO3, Related Products of 82-73-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Gao, Hang’s team published research in Science China: Chemistry in 2020-05-31 | 184239-35-8

Science China: Chemistry published new progress about Electric current-potential relationship. 184239-35-8 belongs to class bromides-buliding-blocks, and the molecular formula is C26H18Br2, Recommanded Product: 1,2-Bis(4-bromophenyl)-1,2-diphenylethene.

Gao, Hang; Zhang, Nan; Li, Yang; Zhao, Wei; Quan, Yiwu; Cheng, Yixiang; Chen, Hong-Yuan; Xu, Jing-Juan published the artcile< Trace Ir(III) complex enhanced electrochemiluminescence of AIE-active Pdots in aqueous media>, Recommanded Product: 1,2-Bis(4-bromophenyl)-1,2-diphenylethene, the main research area is polytetraphenylethene iridium complex Suzuki coupling polymerization electrochemiluminescence.

Trace Ir(III) complex enhanced aggregation-induced electrochemiluminescence (AIECL) of poly-tetraphenylethene (pTPE) in aqueous media was investigated for the first time. The poly-TPE end-capped by Ir(III) complex (Ir@pTPE) and its corresponding model polymer poly-TPE (Ph@pTPE) could be synthesized by Suzuki coupling polymerization reaction of 1,2-bis(4-bromophenyl)- 1,2-diphenylethene (M-1) with 1,2-diphenyl-1,2-bis(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethene (M-2) and the continuous Suzuki coupling end-capped reaction of poly-TPE-pinacol boronate with (pq)2Ir(pico)Br and bromobenzene, resp. Subsequently, the corresponding Ir@pTPE Pdots and Ph@pTPE Pdots encapsulated with poly(styrene- co-maleicanhydride) (PSMA) could be obtained by nano-precipitation method. Compared with Ph@pTPE Pdots, the Ir@pTPE Pdots with a trace amount of Ir(III) complex (1.34‰ of Ir(III) content, wt) could exhibit 9.9-fold enhancement of the electrochemiluminescence (ECL) signal for visual emission. This work provided a novel strategy on designing highly efficient ECL materials based on trace Ir(III)-end capping AIE-active polymer dots. electrochemiluminescence, aggregation-induced emission, Ir(III) complex, polymer dots.

Science China: Chemistry published new progress about Electric current-potential relationship. 184239-35-8 belongs to class bromides-buliding-blocks, and the molecular formula is C26H18Br2, Recommanded Product: 1,2-Bis(4-bromophenyl)-1,2-diphenylethene.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yamano, Ryota’s team published research in Organic Letters in 2017-01-06 | 135999-16-5

Organic Letters published new progress about [2+2+2] Cycloaddition reaction. 135999-16-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H7BrO2, Application of C7H7BrO2.

Yamano, Ryota; Hara, Jun; Murayama, Koichi; Sugiyama, Haruki; Teraoka, Kota; Uekusa, Hidehiro; Kawauchi, Susumu; Shibata, Yu; Tanaka, Ken published the artcile< Rh-Mediated Enantioselective Synthesis, Crystal Structures, and Photophysical/Chiroptical Properties of Phenanthrenol-Based [9]Helicene-like Molecules>, Application of C7H7BrO2, the main research area is enantioselective synthesis phenanthrenol based nonahelicene.

The enantioselective synthesis of phenanthrenol-based [9]helicene-like mols. has been achieved via the rhodium-mediated intramol. [2+2+2] cycloadditions of 3-phenanthrenol-linked triynes. Crystal structures and photophys./chiroptical properties of these [9]helicene-like mols. were compared with the corresponding [7]helicene-like mols.

Organic Letters published new progress about [2+2+2] Cycloaddition reaction. 135999-16-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H7BrO2, Application of C7H7BrO2.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Liang, Yantang’s team published research in Organic Letters in 2019-06-21 | 3959-07-7

Organic Letters published new progress about Aliphatic amines Role: RCT (Reactant), RACT (Reactant or Reagent). 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Category: bromides-buliding-blocks.

Liang, Yantang; Tan, Zhenda; Jiang, Huanfeng; Zhu, Zhibo; Zhang, Min published the artcile< Copper-Catalyzed Oxidative Multicomponent Annulation Reaction for Direct Synthesis of Quinazolinones via an Imine-Protection Strategy>, Category: bromides-buliding-blocks, the main research area is quinazolinone preparation copper catalyst oxidative multicomponent annulation.

Via an imine-protection strategy, the authors herein present an unprecedented copper-catalyzed oxidative multicomponent annulation reaction for direct synthesis of quinazolinones. The construction of various products is achieved via formation of three C-N and one C-C bonds in conjunction with the benzylic functionalization. The merits of easily available feedstocks, naturally abundant catalyst, good functional group and substrate compatibility, and release of H2O as the byproduct make the developed chem. a practical way to access quinazolinones.

Organic Letters published new progress about Aliphatic amines Role: RCT (Reactant), RACT (Reactant or Reagent). 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Category: bromides-buliding-blocks.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yang, Xue’s team published research in Journal of Catalysis in 2019-10-31 | 3959-07-7

Journal of Catalysis published new progress about Electric capacitance. 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Category: bromides-buliding-blocks.

Yang, Xue; Huang, Tao; Gao, Shuiying; Cao, Rong published the artcile< Boosting photocatalytic oxidative coupling of amines by a Ru-complex-sensitized metal-organic framework>, Category: bromides-buliding-blocks, the main research area is oxidative coupling photocatalyst metal organic framework.

Visible-light-driven selective photocatalytic organic synthesis has recently become a topic of great interest due to its environmental friendliness and sustainability. It is demanding for photocatalysis to utilize the wider range of light, such as visible light, and its performance is often plagued by the sluggish separation of photogenerated charge carriers. An approach is now reported to address these issues by incorporating light harvesting RuII-polypyridyl complexes into a semiconductor-type metal-organic framework (MIL-125). Delightedly, the obtained Ru(bpy)3@MIL-125 photocatalyst presents a remarkably stable and high photoactivity toward the selective oxidative coupling of amines under ambient air with visible light irradiation (λ > 440 nm). The mechanistic investigation unveiled that both effectively photoexcited electrons transfer from [Ru(bpy)3]Cl2 to MIL-125 and the interaction of C-H bonds with superoxide radical (O·-2) play a critical role in photo-catalyzing selective aerobic oxidative coupling of amines. This work highlights a significant role of MOFs as heterogeneous photocatalysts in photocatalytic organic transformations.

Journal of Catalysis published new progress about Electric capacitance. 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Category: bromides-buliding-blocks.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Patel, Harun’s team published research in Bioorganic Chemistry in 2020-09-30 | 82-73-5

Bioorganic Chemistry published new progress about Drug toxicity. 82-73-5 belongs to class bromides-buliding-blocks, and the molecular formula is C8H3BrO3, Application In Synthesis of 82-73-5.

Patel, Harun; Chaudhari, Kavita; Jain, Pritam; Surana, Sanjay published the artcile< Synthesis and in vitro antitubercular activity of pyridine analouges against the resistant Mycobacterium tuberculosis>, Application In Synthesis of 82-73-5, the main research area is pyridinyl hydrazide preparation antitubercular activity SAR; Schiff base pyridinyl preparation antitubercular activity SAR; Cytotoxicity; MDR-MTB; Mycobacterium tuberculosis; Synthesis.

Synthesis and the biol. activity of isoniazid and pyridine derivatives were successfully carried out with elaborated characterization by spectral data. Amongst the synthesized compounds; I and II displayed encouraging antimycobacterial activity with IC50 of 3.2μM and 1.5μM against the H37Rv strain. The MIC of test compounds I and II were also assessed against the 5 drug resistant isolates (FQ-R1, INH-R1, INH-R2, RIF-R1 and RIF-R2) of MTB strains under aerobic conditions and compound I [MIC = 3.2μM for FQ-R1; MIC = 140μM for INH-R1; MIC = 160μM for INH-R2; MIC = 2.4μM towards RIF-R1; MIC = 4.2μM for RIF-R2] and II [MIC = 3.3μM for FQ-R1; MIC = 170μM for INH-R1; MIC = 190μM for INH-R2; MIC = 1.8μM for RIF-R1; MIC = 8.4μM for RIF-R2] have shown significant activity at non-cytotoxic concentration in comparison to the standard drug.

Bioorganic Chemistry published new progress about Drug toxicity. 82-73-5 belongs to class bromides-buliding-blocks, and the molecular formula is C8H3BrO3, Application In Synthesis of 82-73-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Vishnumurthy, Kodumuru’s team published research in Journal of Combinatorial Chemistry in 2010-10-31 | 6942-39-8

Journal of Combinatorial Chemistry published new progress about Aromatic carboxylic acids, salts Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 6942-39-8 belongs to class bromides-buliding-blocks, and the molecular formula is C8H6BrFO2, Reference of 6942-39-8.

Vishnumurthy, Kodumuru; Makriyannis, Alexandros published the artcile< Novel and efficient one-step parallel synthesis of dibenzopyranones via Suzuki-Miyaura cross coupling>, Reference of 6942-39-8, the main research area is dibenzopyranone preparation; bromoarylcarboxylate hydroxyarylboronic acid Suzuki Miyaura coupling lactonization.

Microwave-promoted novel and efficient one-step parallel synthesis of dibenzopyranones and heterocyclic analogs from bromo arylcarboxylates and o-hydroxyarylboronic acids via Suzuki-Miyaura cross coupling reaction is described. Spontaneous lactonization gave dibenzopyranones and heterocyclic analogs bearing electron-donating and -withdrawing groups on both aromatic rings in good to excellent yields.

Journal of Combinatorial Chemistry published new progress about Aromatic carboxylic acids, salts Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 6942-39-8 belongs to class bromides-buliding-blocks, and the molecular formula is C8H6BrFO2, Reference of 6942-39-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Li, Peiyu’s team published research in Materials Today Chemistry in 2022-09-30 | 3959-07-7

Materials Today Chemistry published new progress about Anaerobic oxidation. 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Related Products of 3959-07-7.

Li, Peiyu; Dong, Xiaoyun; Zhang, Ya; Lang, Xianjun; Wang, Cheng published the artcile< An azine-linked 2D porphyrinic covalent organic framework for red light photocatalytic oxidative coupling of amines>, Related Products of 3959-07-7, the main research area is azine porphyrinic covalent organic framework benzylamine photocatalytic oxidative coupling.

The construction of two-dimensional covalent organic frameworks (2D COFs) with robust stability for photocatalysis has gained intensive attention recently. Herein, we report the design and synthesis of a highly crystalline azine-linked porphyrinic 2D COF (Por-HZ-COF). Our results clearly show that Por-HZ-COF adopts an eclipsed AA stacking structure with a high Brunauer-Emmett-Teller (BET) sp. surface area of 1586 m2/g. In addition, Por-HZ-COF is chem. stable under various conditions, even in 12 M sodium hydroxide aqueous solution or 9 M hydrochloric acid. Moreover, Por-HZ-COF can be used for the photocatalytic aerobic oxidative coupling of benzylamines under red light irradiation with high activity and good reusability. This study demonstrates a novel robust 2D COF with azine linkage that has promising applications in photocatalysis.

Materials Today Chemistry published new progress about Anaerobic oxidation. 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Related Products of 3959-07-7.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Adhikary, Saswati’s team published research in ACS Omega in 2020-06-23 | 3959-07-7

ACS Omega published new progress about Aldehydes Role: RCT (Reactant), RACT (Reactant or Reagent). 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Name: 4-Bromobenzylamine.

Adhikary, Saswati; Majumder, Leena; Pakrashy, Sourav; Srinath, Ravuri; Mukherjee, Kaustuv; Mandal, Chitra; Banerji, Biswadip published the artcile< Polysubstituted Imidazoles as LysoTracker Molecules: Their Synthesis via Iodine/H2O and Cell-Imaging Studies>, Name: 4-Bromobenzylamine, the main research area is imidazole regioselective synthesis fluorescent lysosome staining probe.

An iodine-catalyzed, environmentally benign one-pot methodol. has been developed for the synthesis of diverse substituted imidazoles. This transition-metal-free, aerobic, water-mediated cyclization reaction is operationally simple and works well with different amines or aldehydes by multiple C-N bond formations with satisfactory yield. The methodol. is regioselective as well as scalable. These imidazole derivatives show excellent fluorescence properties both in the solid and solution phase, which is further extended to live-cell imaging. Due to the suitable fluorescence properties of these scaffolds, lysosome-directing groups are incorporated in two of these derivatized imidazoles to track intracellular lysosomes. Successfully, those mols. show bright blue fluorescence while detecting lysosomes in human or murine cells and can be considered to be rapid lysosome-staining probes.

ACS Omega published new progress about Aldehydes Role: RCT (Reactant), RACT (Reactant or Reagent). 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Name: 4-Bromobenzylamine.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary