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(4-Methoxy-3-nitro-phenyl)-(3-trifluoromethyl-phenyl)-methanone is a complex organic compound characterized by its molecular formula C15H10F3NO4. (4-Methoxy-3-nitro-phenyl)-(3-trifluoromethyl-phenyl)-methanone features a methanone (or ketone) functional group, which is a carbonyl group (C=O) bonded to two carbon atoms. One of the phenyl rings is substituted with a 4-methoxy group, which is a methoxy (-OCH3) group attached at the 4th position, and a 3-nitro group, which is a nitro (-NO2) group attached at the 3rd position. The other phenyl ring is substituted with a 3-trifluoromethyl group, which is a trifluoromethyl (-CF3) group attached at the 3rd position. (4-Methoxy-3-nitro-phenyl)-(3-trifluoromethyl-phenyl)-methanone is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, and it is also of interest in chemical research due to its unique structure and properties.

66938-44-1

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66938-44-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66938-44-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,3 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66938-44:
(7*6)+(6*6)+(5*9)+(4*3)+(3*8)+(2*4)+(1*4)=171
171 % 10 = 1
So 66938-44-1 is a valid CAS Registry Number.

66938-44-1Relevant academic research and scientific papers

Synthesis and anthelminthic acitivity of alkyl-(5-acyl-1-benzimidazol-2-yl) carbamates

Raeymackers,Van Gelder,Roevens,Janssen

, p. 586 - 594 (2007/10/05)

A series of alkyl-(5-acyl-l-H-benzimidazol-2-yl)-carbamates were prepared and screened for anthelminthic activity. Some of them were found to be fully active at low, atoxic oral dose levels against gastro-intestinal nematodes. The activity against Syphacia muris and Strongyloides ratta is indicated. From these studies methyl (5-benzoyl-1-H-benzimidazol-2-yl) carbamate (mebendazole) and methyl [5-(4-fluorobenzoyl)-1-H-benzimidazol-2-yl]carbamate (flubendazole) were selected for detailed investigation.

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