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1-(4-tert-butylphenyl)-2-(1H-imidazol-1-yl)ethan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73932-06-6

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73932-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73932-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,3 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73932-06:
(7*7)+(6*3)+(5*9)+(4*3)+(3*2)+(2*0)+(1*6)=136
136 % 10 = 6
So 73932-06-6 is a valid CAS Registry Number.

73932-06-6Relevant academic research and scientific papers

Diaryl-containing imidazole compound and preparation method and medical application thereof

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Paragraph 0138; 0141; 0142, (2019/02/21)

The invention discloses a diaryl-containing imidazole compound. The invention further discloses application of the diaryl-containing imidazole compound to preparation of drugs for preventing or treating Alzheimer's disease. The inventor screens butyrylcholine esterase and IDO1 as carriers for inhibiting the activity to evaluate the effect of the diaryl imidazole compound to treat Alzheimer's disease, and finds that the diaryl imidazole compound has good in vitro activity, and can be further developed as a precursor substance for performing the Alzheimer's disease resistant effect by inhibitingthe activity of cholinesterase. (The formula is shown in the description).

Synthesis and anticonvulsant activity of N-(benzoylalkyl)imidazoles and N-(ω-phenyl-ω-hydroxyalkyl)imidazoles

Nardi,Tajana,Leonardi,Pennini,Portioli,Magistretti,Subissi

, p. 727 - 731 (2007/10/02)

A novel series of N-(benzoylalkyl)imidazoles and N-(ω-phenyl-ω-hydroxyalkyl)imidazoles was synthesized and evaluated for anticonvulsant activity in mice against maximal electroshock induced seizures. Some of the compounds showed an activity comparable to or better than phenytoin and phenobarbital. The N-[β-[4-(β-phenylethyl)phenyl]-β-hydroxyethyl]imidazole (38) was selected for further studies; preclinical toxicology and additional efficacy evaluations are in progress. Structure-activity relationships are discussed.

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