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1H-Benzimidazole, 2-(4-ethylphenyl)-5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67273-58-9

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67273-58-9 Usage

Chemical Family

Belongs to the benzimidazole family

Structure

Composed of a benzene ring fused with an imidazole ring

Substituents

Methyl group at the 5th position and a 4-ethylphenyl group at the 2nd position

Applications

Commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals

Reactivity

Exhibits versatile reactivity

Pharmacological Potential

Possesses pharmacological potential

Biological Activities

Exhibits antimicrobial, anticancer, and antiviral properties

Drug Discovery

Valued candidate for drug discovery and development

Organic Synthesis

Utilized as a synthetic intermediate for the preparation of diverse functionalized molecules

Check Digit Verification of cas no

The CAS Registry Mumber 67273-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,7 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67273-58:
(7*6)+(6*7)+(5*2)+(4*7)+(3*3)+(2*5)+(1*8)=149
149 % 10 = 9
So 67273-58-9 is a valid CAS Registry Number.

67273-58-9Downstream Products

67273-58-9Relevant academic research and scientific papers

Tunable Triazole-Phosphine-Copper Catalysts for the Synthesis of 2-Aryl-1H-benzo[d]imidazoles from Benzyl Alcohols and Diamines by Acceptorless Dehydrogenation and Borrowing Hydrogen Reactions

Xu, Zhaojun,Wang, Duo-Sheng,Yu, Xiaoli,Yang, Yongchun,Wang, Dawei

, p. 3332 - 3340 (2017)

Triazole-phosphine-copper complexes (TAP?Cu) have been synthesized and applied as tunable and efficient catalysts for the selective synthesis of fluoro-substituted 2-aryl-1H-benzo[d]imidazole and 1-benzyl-2-aryl-1H-benzo[d]imidazole derivatives from simple alcohols in only one step. TAP?Cu exhibited excellent and tunable catalytic activity for both dehydrogenation and borrowing hydrogen reactions with more than 80 examples being demonstrated for the first time. It was observed that the ligand played a critical role in catalyst activity. Mechanistic studies and deuterium labeling experiments indicated that the reactions proceeded by an initial and reversible alcohol dehydrogenation resulting in a copper hydride intermediate. This was also supported by the direct observation of a diagnostic copper hydride signal by solid-state infrared spectroscopy. The TAP?Cu-H complex showed absorptions at 912 cm?1 that could be assigned to copper?hydride stretches. Furthermore, the direct trapping of an intermediate bisimine was also successfully performed. (Figure presented.).

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