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1-Propanone, 3-(1H-benzimidazol-2-yl)-1-phenyl- is a complex organic compound with the chemical formula C17H14N2O. It is a derivative of propanone, featuring a benzimidazole ring and a phenyl group attached to the carbonyl group. 1-Propanone, 3-(1H-benzimidazol-2-yl)-1-phenyl- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving propanone and benzimidazole, and its properties, such as solubility and stability, can vary depending on the specific conditions of the synthesis. The compound's structure and potential applications make it an interesting subject for research in the field of organic chemistry.

5805-55-0

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5805-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5805-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,0 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5805-55:
(6*5)+(5*8)+(4*0)+(3*5)+(2*5)+(1*5)=100
100 % 10 = 0
So 5805-55-0 is a valid CAS Registry Number.

5805-55-0Relevant academic research and scientific papers

Synthesis of 2-(3-furyl)-1H-benzimidazoles from 2-phenacyl-1H- benzimidazoles

Dzvinchuk,Lozinskii

, p. 1390 - 1396 (2008/09/19)

C-Alkylation at the active methylene group of 2-phenacyl-1H-benzimidazoles with phenacyl bromides proceeds highly selectively with the formation of the corresponding 1,4-diketones, which on heating with hydrochloric acid are cyclized with the formation of the previously unknown 2-(2,5-diaryl-3-furyl)-1H- benzimidazoles.

Reaction of 2-chloromethylbenzimidazoles with acetylacetone and benzoylacetone. Basic breakdown of β-diketones

Popov

, p. 918 - 922 (2007/10/03)

Base treatment of the products of alkylalion of β-diketones by 2-chloromethylbenzimidazole under phase transfer catalysis (PTC) conditions causes loss of the acetyl group and formation of methylethyl- or ethylphenyl ketones. 1997 Plenum Publishing Corpora

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