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N-(4-trifluoroacetyl-phenyl)-isobutyramide is a chemical compound with the molecular formula C11H10F3NO3. It is a derivative of isobutyramide, featuring a 4-trifluoroacetyl-phenyl group attached to the nitrogen atom. N-(4-trifluoroacetyl-phenyl)-isobutyramide is characterized by its aromatic ring structure with a trifluoroacetyl group, which imparts unique electronic and steric properties. It is synthesized through a reaction between isobutyramide and 4-trifluoroacetyl-phenyl, and it may have applications in the fields of pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. The compound's properties, such as solubility, stability, and reactivity, can be influenced by the presence of the trifluoromethyl groups, making it a potentially interesting molecule for further study and development.

74696-68-7

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74696-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74696-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,9 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74696-68:
(7*7)+(6*4)+(5*6)+(4*9)+(3*6)+(2*6)+(1*8)=177
177 % 10 = 7
So 74696-68-7 is a valid CAS Registry Number.

74696-68-7Downstream Products

74696-68-7Relevant academic research and scientific papers

Novel trifluoroacetophenone derivatives as malonyl-CoA decarboxylase inhibitors

Wallace, David M.,Haramura, Masayuki,Cheng, Jie-Fei,Arrhenius, Thomas,Nadzan, Alex M.

, p. 1127 - 1130 (2007/10/03)

A series of trifluoroacetophenone derivatives were prepared and evaluated as malonyl-CoA decarboxylase (MCD) inhibitors. Some of the 'reverse amide' analogs were found to be potent inhibitors of MCD enzyme activity. The trifluoroacetyl group may interact with the MCD active site as the hydrate in a similar fashion to the hexafluoroisopropanol analogs reported previously. Adding electron-withdrawing groups to the phenyl ring stabilizes the hydrated species and enhances this interaction.

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