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2-(2-bromo-phenyl)-1-thiophen-2-yl-ethanone is a complex organic chemical compound characterized by its unique molecular structure. It is a derivative of acetophenone, with a bromine atom attached to the phenyl ring and a thiophene ring fused to the ethanone moiety. 2-(2-bromo-phenyl)-1-thiophen-2-yl-ethanone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its reactive functional groups. The presence of the bromine atom makes it a valuable intermediate for further chemical reactions, such as cross-coupling or substitution reactions, which can lead to the formation of a diverse range of molecules with different properties and applications. The compound's structure also suggests that it may have interesting electronic and steric properties, which could be explored in the context of materials science or as a precursor to more complex organic molecules.

5062-07-7

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5062-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5062-07-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5062-07:
(6*5)+(5*0)+(4*6)+(3*2)+(2*0)+(1*7)=67
67 % 10 = 7
So 5062-07-7 is a valid CAS Registry Number.

5062-07-7Downstream Products

5062-07-7Relevant academic research and scientific papers

Two-Step One-Pot Synthesis of Unsymmetrical (Hetero)Aryl 1,2-Diketones by Addition-Oxygenation of Potassium Aryltrifluoroborates to (Hetero)Arylacetonitriles

Kumar, Yogesh,Jaiswal, Yogesh,Kumar, Amit

, p. 494 - 505 (2018)

An efficient one-pot two-step procedure for the synthesis of unsymmetrical (hetero)aryl 1,2-diketones has been developed. The reaction proceeds through a palladium-catalyzed nucleophilic addition of potassium aryltrifluoroborates to aliphatic nitriles followed by a copper-catalyzed aerobic benzylic C–H oxygenation using molecular oxygen as a green oxidant. This represents the first example of the direct synthesis of unsymmetrical diaryl 1,2-diketones from arylacetonitriles. This method utilizes inexpensive, stable, nontoxic, and readily available starting materials, is highly effective in the presence of both electron-rich and electron-poor nitriles and aryltrifluoroborates, and tolerates a wide variety of functional groups. The synthetic utility of this transformation was shown by increasing the scale of the reaction and by carrying out the one-pot protocol for the preparation of quinoxaline and benzimidazole derivatives. A plausible reaction mechanism has also been proposed.

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