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2-(2-bromo-4-chlorophenyl)quinoline is a complex organic compound characterized by its unique molecular structure, which consists of a quinoline ring system fused with a bromo-chlorophenyl group. 2-(2-bromo-4-chlorophenyl)quinoline is notable for its halogenated aromatic nature, featuring a bromine atom at the 2-position and a chlorine atom at the 4-position of the phenyl ring. The presence of these halogens can significantly influence the compound's reactivity, solubility, and potential applications in various chemical and pharmaceutical processes. Due to its specific structure, 2-(2-bromo-4-chlorophenyl)quinoline may be utilized in the synthesis of more complex molecules or as an intermediate in the production of pharmaceuticals, agrochemicals, or other specialty chemicals. Its properties, such as electronic effects and steric hindrance, make it a valuable building block in organic synthesis, particularly in the development of new compounds with tailored properties.

958-69-0

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958-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 958-69-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 958-69:
(5*9)+(4*5)+(3*8)+(2*6)+(1*9)=110
110 % 10 = 0
So 958-69-0 is a valid CAS Registry Number.

958-69-0Downstream Products

958-69-0Relevant academic research and scientific papers

Enantioselective Dearomative [3 + 2] Umpolung Annulation of N-Heteroarenes with Alkynes

Cui, Bing-Hui,Huang, Wen-Yu,Jia, Yi-Xia,Liang, Ren-Xiao,Liu, Hang,Liu, Jia-Liang,Wang, Qiang,Yang, Peng,Zhang, Xiao-Dong,Zhang, Yue-Yuan

, p. 1087 - 1093 (2022/02/09)

Enantioselective [3 + 2] annulation of N-heteroarenes with alkynes has been developed via a cobalt-catalyzed dearomative umpolung strategy in the presence of chiral ligand and reducing reagent. A variety of electron-deficient N-heteroarenes, including qui

A Novel Route to 2-Arylquinolines: Reductive Cleavage of 2′-Nitroaryl-Δ2 -isoxazolines

Kamath, Prashantha,Viner, Russell C.,Smith, Stephen C.,Lal, Mukul

, p. 1341 - 1345 (2017/06/27)

A novel synthetic route for the synthesis of quinolines starting from Δ 2 -isoxazolines under reductive conditions is reported. The reductive cyclization to quinolines is achieved under both metal and metal-free conditions. The reaction proceeds via an intramolecular N-H?O hydrogen bond intermediate, accelerating the reductive cleavage 1000-fold (DFT calculations) in comparison with non-hydrogen bonded system.

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