Duong, Hung A.’s team published research in Organometallics in 2017 | CAS: 53939-30-3

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. In industry and in the lab, pyridine is used as a reaction solvent, particularly when its basicity is useful, and as a starting material for synthesizing some herbicides, fungicides, and antiseptics.Computed Properties of C5H3BrClN

In 2017,Duong, Hung A.; Wu, Wenqin; Teo, Yu-Yuan published 《Cobalt-Catalyzed Cross-Coupling Reactions of Arylboronic Esters and Aryl Halides》.Organometallics published the findings.Computed Properties of C5H3BrClN The information in the text is summarized as follows:

An efficient cobalt catalyst system for the Suzuki-Miyaura cross-coupling reaction of arylboronic esters and aryl halides has been identified. In the presence of cobalt(II)/terpyridine catalyst and potassium methoxide, a diverse array of (hetero)biaryls have been prepared in moderate to excellent yields. In the experimental materials used by the author, we found 5-Bromo-2-chloropyridine(cas: 53939-30-3Computed Properties of C5H3BrClN)

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. In industry and in the lab, pyridine is used as a reaction solvent, particularly when its basicity is useful, and as a starting material for synthesizing some herbicides, fungicides, and antiseptics.Computed Properties of C5H3BrClN

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Deutsch, Amrei’s team published research in Organic Letters in 2016 | CAS: 53939-30-3

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. Pyridines form stable salts with strong acids. Pyridine itself is often used to neutralize acid formed in a reaction and as a basic solvent. Recommanded Product: 5-Bromo-2-chloropyridine

In 2016,Deutsch, Amrei; Jessen, Christoph; Deutsch, Carl; Karaghiosoff, Konstantin; Hoffmann-Roeder, Anja published 《One-Pot Synthesis of Substituted Trifluoromethylated 2,3-Dihydro-1H-imidazoles》.Organic Letters published the findings.Recommanded Product: 5-Bromo-2-chloropyridine The information in the text is summarized as follows:

An operationally simple one-pot reaction for the preparation of a novel class of racemic trifluoromethylated 2,3-dihydro-1H-imidazoles derived from electron-poor N,O-acetals and aryl Grignard reagents is described. In addition, access to highly functionalized 2-trifluoromethyl-2,3-dihydro-1H-imidazoles was accomplished by reaction of N-aryl hemiaminal ethers and N-aryl trifluoroethylamines in the presence of an excess of n-butyllithium. In the part of experimental materials, we found many familiar compounds, such as 5-Bromo-2-chloropyridine(cas: 53939-30-3Recommanded Product: 5-Bromo-2-chloropyridine)

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. Pyridines form stable salts with strong acids. Pyridine itself is often used to neutralize acid formed in a reaction and as a basic solvent. Recommanded Product: 5-Bromo-2-chloropyridine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Ryan, Sarah J.’s team published research in Organic Letters in 2015 | CAS: 53939-30-3

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. Pyridine is very deactivated towards electrophilic substitution with respect to benzene. For this reason classical formylation, using methods such as the Gattermann or Vilsmeier reactions, are not generally successful. COA of Formula: C5H3BrClN

In 2015,Ryan, Sarah J.; Schimler, Sydonie D.; Bland, Douglas C.; Sanford, Melanie S. published 《Acyl Azolium Fluorides for Room Temperature Nucleophilic Aromatic Fluorination of Chloro- and Nitroarenes》.Organic Letters published the findings.COA of Formula: C5H3BrClN The information in the text is summarized as follows:

The reaction of acid fluorides with N-heterocyclic carbenes (NHCs) produces anhydrous acyl azolium fluorides. With appropriate selection of the acid fluoride and NHC, these salts can be used for the room temperature SNAr fluorination of a variety of aryl chlorides and nitroarenes. E.g., in presence of N-heterocyclic carbene (I) and 4-MeOC6H4COF, fluorination of aryl chloride (II) gave 99% aryl fluoride (III). In the experiment, the researchers used 5-Bromo-2-chloropyridine(cas: 53939-30-3COA of Formula: C5H3BrClN)

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. Pyridine is very deactivated towards electrophilic substitution with respect to benzene. For this reason classical formylation, using methods such as the Gattermann or Vilsmeier reactions, are not generally successful. COA of Formula: C5H3BrClN

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Liang, Ren-Xiao’s team published research in ACS Catalysis in 2021 | CAS: 39856-58-1

2-Bromopyridin-3-amine(cas: 39856-58-1) belongs to anime. Reaction with nitrous acid (HNO2), which functions as an acylating agent that is a source of the nitrosyl group (―NO), converts aliphatic primary amines to nitrogen and mixtures of alkenes and alcohols corresponding to the alkyl group in a complex process. This reaction has been used for analytical determination of primary amino groups in a procedure known as the Van Slyke method.Recommanded Product: 2-Bromopyridin-3-amine

Liang, Ren-Xiao; Zhong, Chao; Liu, Zhi-Hong; Yang, Miao; Tang, Heng-Wei; Chen, Jian-Fei; Yang, Yun-Fang; Jia, Yi-Xia published an article on February 5 ,2021. The article was titled 《Enantioselective Arylation of Tetrasubstituted Enamines: Access to Enantioenriched Indolenine and 1H-Indole Derivatives》, and you may find the article in ACS Catalysis.Recommanded Product: 2-Bromopyridin-3-amine The information in the text is summarized as follows:

Palladium-catalyzed intramol. enantioselective β-arylation of tetrasubstituted endocyclic and exocyclic enamines was developed. A range of optically active medium-ring fused indolenines or 3,3′-spiroindolenines were achieved in enantiomeric ratios up to 98:2 with Cs2CO3 or K3PO4 as the base in the presence of chiral PHOX ligands. The use of Ag3PO4 as a base led to enantioenriched 1H-indoles in good enantiomeric ratios (up to 89:11) with (S)-DIFLUORPHOS as a chiral ligand, which proceeded via a possible domino enamine-isomerization/β-arylation sequence. The experimental part of the paper was very detailed, including the reaction process of 2-Bromopyridin-3-amine(cas: 39856-58-1Recommanded Product: 2-Bromopyridin-3-amine)

2-Bromopyridin-3-amine(cas: 39856-58-1) belongs to anime. Reaction with nitrous acid (HNO2), which functions as an acylating agent that is a source of the nitrosyl group (―NO), converts aliphatic primary amines to nitrogen and mixtures of alkenes and alcohols corresponding to the alkyl group in a complex process. This reaction has been used for analytical determination of primary amino groups in a procedure known as the Van Slyke method.Recommanded Product: 2-Bromopyridin-3-amine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Yang, Yu-Ming’s team published research in Organic Letters in 2019 | CAS: 39856-58-1

2-Bromopyridin-3-amine(cas: 39856-58-1) belongs to anime. Amine, any member of a family of nitrogen-containing organic compounds that is derived, either in principle or in practice, from ammonia (NH3). Naturally occurring amines include the alkaloids, which are present in certain plants; the catecholamine neurotransmitters (i.e., dopamine, epinephrine, and norepinephrine); and a local chemical mediator, histamine, that occurs in most animal tissues.Formula: C5H5BrN2

Formula: C5H5BrN2On October 4, 2019 ,《Silver-Mediated Trifluoromethoxylation of (Hetero)aryldiazonium Tetrafluoroborates》 was published in Organic Letters. The article was written by Yang, Yu-Ming; Yao, Jian-Fei; Yan, Wei; Luo, Zhuangzhu; Tang, Zhen-Yu. The article contains the following contents:

Here we report a silver-mediated trifluoromethoxylation of (hetero)aryldiazonium tetrafluoroborates by converting an aromatic amino group into an OCF3 group. This method, which can be considered to be a trifluoromethoxylation variation of the classic Sandmeyer-type reaction, uses readily available aryl and heteroaromatic amines as starting materials and AgOCF3 as trifluoromethoxylating reagents. The broad substrate scope and simple, mild reaction condition made this transformation a valuable method in constructing aryl-OCF3 bonds. In addition to this study using 2-Bromopyridin-3-amine, there are many other studies that have used 2-Bromopyridin-3-amine(cas: 39856-58-1Formula: C5H5BrN2) was used in this study.

2-Bromopyridin-3-amine(cas: 39856-58-1) belongs to anime. Amine, any member of a family of nitrogen-containing organic compounds that is derived, either in principle or in practice, from ammonia (NH3). Naturally occurring amines include the alkaloids, which are present in certain plants; the catecholamine neurotransmitters (i.e., dopamine, epinephrine, and norepinephrine); and a local chemical mediator, histamine, that occurs in most animal tissues.Formula: C5H5BrN2

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Ferlin, Francesco’s team published research in ChemSusChem in 2022 | CAS: 39856-58-1

2-Bromopyridin-3-amine(cas: 39856-58-1) belongs to anime.Typically the presence of an amine functional group is deduced by a combination of techniques, including mass spectrometry as well as NMR and IR spectroscopies. 1H NMR signals for amines disappear upon treatment of the sample with D2O. In their infrared spectrum primary amines exhibit two N-H bands, whereas secondary amines exhibit only one.Application In Synthesis of 2-Bromopyridin-3-amine

Application In Synthesis of 2-Bromopyridin-3-amineOn March 22, 2022, Ferlin, Francesco; Anastasiou, Ioannis; Salameh, Nihad; Miyakoshi, Takeru; Baudoin, Olivier; Vaccaro, Luigi published an article in ChemSusChem. The article was 《C(sp3)-H Arylation Promoted by a Heterogeneous Palladium-N-Heterocyclic Carbene Complex in Batch and Continuous Flow》. The article mentions the following:

A heterogeneous reusable palladium(II)-bis(N-heterocyclic carbene) catalyst was prepared and shown to catalyze the intramol. C(sp3)-H activation/cyclization of N-alkyl-2-bromoanilines furnishing indolines. This new catalytic system was based on a bis-imidazolium ligand immobilized on a spaced cross-linked polystyrene support. The iodide ligands on the catalyst played a central role in the efficiency of the process occurring through a “”release and catch”” mechanism. The heterogeneous nature of the catalyst was further exploited in the design of a continuous-flow protocol that allowed a more efficient recovery and reuse of the catalyst, as well as a very fast and safe procedure. In addition to this study using 2-Bromopyridin-3-amine, there are many other studies that have used 2-Bromopyridin-3-amine(cas: 39856-58-1Application In Synthesis of 2-Bromopyridin-3-amine) was used in this study.

2-Bromopyridin-3-amine(cas: 39856-58-1) belongs to anime.Typically the presence of an amine functional group is deduced by a combination of techniques, including mass spectrometry as well as NMR and IR spectroscopies. 1H NMR signals for amines disappear upon treatment of the sample with D2O. In their infrared spectrum primary amines exhibit two N-H bands, whereas secondary amines exhibit only one.Application In Synthesis of 2-Bromopyridin-3-amine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Shi, Jing’s team published research in Chemistry Letters in 2007 | CAS: 1094679-27-2

4-Ethynylpyridin-2-amine(cas: 1094679-27-2) belongs to anime. Examples of direct uses of amines and their salts are as corrosion inhibitors in boilers and in lubricating oils (morpholine), as antioxidants for rubber and roofing asphalt (diarylamines), as stabilizers for cellulose nitrate explosives (diphenylamine), as protectants against damage from gamma radiation (diarylamines), as developers in photography (aromatic diamines), as flotation agents in mining, as anticling and waterproofing agents for textiles, as fabric softeners, in paper coating, and for solubilizing herbicides.Category: pyridine-derivatives

Category: pyridine-derivativesOn September 5, 2007 ,《Facile derivatization of pyridyloxazole-type fluorophore via click chemistry》 was published in Chemistry Letters. The article was written by Shi, Jing; Liu, Lei; He, Jing; Meng, Xiangming; Guo, Qingxiang. The article contains the following contents:

New derivatives of the arylpyridyloxazole-type fluorophore were synthesized in high efficiency through click chem. This method is potentially useful for the combinatory screening of fluorescent labels to target specific biol. processes. Using this method, we successfully developed three new pyrazole ratiometric dual-fluorescent pH sensors.4-Ethynylpyridin-2-amine(cas: 1094679-27-2Category: pyridine-derivatives) was used in this study.

4-Ethynylpyridin-2-amine(cas: 1094679-27-2) belongs to anime. Examples of direct uses of amines and their salts are as corrosion inhibitors in boilers and in lubricating oils (morpholine), as antioxidants for rubber and roofing asphalt (diarylamines), as stabilizers for cellulose nitrate explosives (diphenylamine), as protectants against damage from gamma radiation (diarylamines), as developers in photography (aromatic diamines), as flotation agents in mining, as anticling and waterproofing agents for textiles, as fabric softeners, in paper coating, and for solubilizing herbicides.Category: pyridine-derivatives

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Xu, Yiwen’s team published research in Tetrahedron Letters in 2020 | CAS: 53939-30-3

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.Name: 5-Bromo-2-chloropyridine

《Metal free [4+1] and [5+1] annulation reactions to prepare heterocycles using DMF and its derivatives as one-carbon source》 was written by Xu, Yiwen; Shen, Bei; Liu, Lingfeng; Qiao, Chunhua. Name: 5-Bromo-2-chloropyridineThis research focused ontriazolopyridine preparation; hydrazinylpyridine amide annulation imidazolium chloride catalyst; triazine preparation; biguanide amide annulation imidazolium chloride catalyst. The article conveys some information:

A highly efficient and practical method using DMF and its derivative for the [4+1] and [5+1] annulation reactions to prepare 1,2,4-triazolo[3,4-a]pyridines, e.g., I and triazines II [R = H, Me, Ph, 2-MeC6H4, 3-ClC6H4; R1 = H, Me; RR1 = (CH2)2O(CH2)2; R2 = H, Ph] was reported. This metal free reaction took advantages of shelf stable DMF as solvent and carbon donor, imidazolium chloride as a catalyst, the mild reaction condition tolerated a broad substrate range and substitutes. The prepared 3-unsubstituted 1,2,4-triazolo[3,4-a]pyridine and derivatives allowed further introduction of a variety of functional groups at 3-position.5-Bromo-2-chloropyridine(cas: 53939-30-3Name: 5-Bromo-2-chloropyridine) was used in this study.

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.Name: 5-Bromo-2-chloropyridine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Yu, Renyou’s team published research in Dalton Transactions in 2021 | CAS: 1134-35-6

4,4′-Dimethyl-2,2′-bipyridine(cas: 1134-35-6) is used in the synthesis of a series of o-phenanthroline-substituted ruthenium(II) complexes.Electric Literature of C12H12N2 Furthermore, 4,4′-Dimethyl-2,2′-bipyridine is used as a chemical Intermediate. It can be used for the determination of ferrous and cyanide compounds.

《Green to blue-green-emitting cationic iridium complexes with a CF3-substituted phenyl-triazole type cyclometalating ligand: synthesis, characterization and their use for efficient light-emitting electrochemical cells》 was written by Yu, Renyou; Song, Yongjun; Chen, Mengzhen; He, Lei. Electric Literature of C12H12N2This research focused ontrifluoromethyl phenyltriazole green preparation iridium complexation; cyclometalated trifluoromethyl phenyltriazole iridium complex preparation electrochem cell; crystal mol structure electroluminescence cyclometalated trifluoromethyl phenyltriazole iridium complex. The article conveys some information:

Green to blue-green-emitting cationic iridium complexes free of sp2 C-F bonds, namely [Ir(CF3-dPhTAZ)2(bpy)]PF6 (1), [Ir(CF3-dPhTAZ)2(dmebpy)]PF6 (2) and [Ir(CF3-dPhTAZ)2(phpyim)]PF6 (3), have been designed and synthesized with 3,4-diphenyl-5-(trifluoromethyl)-4H-1,2,4-triazole (CF3-dPhTAZ) as the cyclometalating ligand (C^N) and 2,2′-bipyridine (bpy), 4,4′-dimethyl-2,2′-bipyridine (dmebpy) or 2-(1-phenyl-1H-imidazol-2-yl)pyridine (phpyim) as the ancillary ligand (N^N). In CH3CN solution, complexes 1-3 afford green to blue-green emission centered at 521, 508 and 498 nm, resp. The electron-withdrawing CF3 group attached at the triazole ring in CF3-dPhTAZ largely blue-shifts (by over 20 nm) the emission of the complex through stabilizing the HOMO. In doped films, the complexes afford sky-blue emission with near-unity phosphorescent efficiencies. In neat films, the complexes show largely suppressed phosphorescence concentration-quenching, with phosphorescent efficiencies of up to 0.66. Theor. calculations reveal that the emission of the complexes can arise from either charge-transfer (Ir → C^N/C^N → N^N) or C^N/N^N-centered 3π-π* states, depending on the local environment of the complexes. Solid-state light-emitting electrochem. cells (LECs) based on the complexes afford green to blue-green electroluminescence centered at 525, 517 and 509 nm, resp., with high current efficiencies of up to 35.1 cd A-1. The work reveals that CF3-dPhTAZ is a promising C^N ligand free of sp2 C-F bonds for constructing efficient cationic iridium complexes with blue-shifted emission. In the experiment, the researchers used many compounds, for example, 4,4′-Dimethyl-2,2′-bipyridine(cas: 1134-35-6Electric Literature of C12H12N2)

4,4′-Dimethyl-2,2′-bipyridine(cas: 1134-35-6) is used in the synthesis of a series of o-phenanthroline-substituted ruthenium(II) complexes.Electric Literature of C12H12N2 Furthermore, 4,4′-Dimethyl-2,2′-bipyridine is used as a chemical Intermediate. It can be used for the determination of ferrous and cyanide compounds.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Song, A-Xiang’s team published research in Organometallics in 2020 | CAS: 53939-30-3

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.Synthetic Route of C5H3BrClN

《Direct (Hetero)arylation of Heteroarenes Catalyzed by Unsymmetrical Pd-PEPPSI-NHC Complexes under Mild Conditions》 was written by Song, A-Xiang; Zeng, Xiao-Xiao; Ma, Bei-Bei; Xu, Chang; Liu, Feng-Shou. Synthetic Route of C5H3BrClNThis research focused onunsym palladium heterocyclic carbene PEPPSI complex preparation arylation catalyst; crystal structure unsym palladium heterocyclic carbene PEPPSI type complex; mol structure unsym palladium heterocyclic carbene PEPPSI type complex; palladium carbene catalyzed heteroarylation heteroarene; muscle relaxant drug dantrolene conjugated mesopolymer preparation. The article conveys some information:

With the aim of developing a facile and efficient method to access structurally intriguing and valuable functionalized (hetero)aryls, two unsym. Pd-PEPPSI-type NHC complexes (PEPPSI, pyridine-enhanced precatalyst preparation, stabilization, and initiation; NHC, N-heterocyclic carbene) were designed and synthesized to catalyze the direct arylation of heteroarenes with (hetero)aryl bromides. The use of this unsym. strategy led to much higher efficiency in comparison to the commonly used C2-sym. Pd-PEPPSI-type NHC complexes. Also, a broad range of heteroaromatics and (hetero)aryl bromide partners with a wide variety of functional groups were all amenable to the developed protocol even at ≥0.05 mol % catalyst loading and under aerobic conditions. More importantly, along with the authors’ study, also the present protocol could provide expedient access to the gram-scale synthesis of the muscle relaxant drug dantrolene and conjugated mesopolymers. The experimental process involved the reaction of 5-Bromo-2-chloropyridine(cas: 53939-30-3Synthetic Route of C5H3BrClN)

5-Bromo-2-chloropyridine(cas: 53939-30-3) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.Synthetic Route of C5H3BrClN

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem