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N-(5-bromo-2-(trifluoromethyl)phenyl)acetamide is a chemical compound with the molecular formula C9H7BrF3NO. It is a derivative of acetamide, featuring a 5-bromo-2-(trifluoromethyl)phenyl group attached to the nitrogen atom. N-(5-bromo-2-(trifluoromethyl)phenyl)acetamide is characterized by its unique structure, which includes a bromine atom at the 5-position and a trifluoromethyl group at the 2-position of the phenyl ring. The presence of these functional groups imparts specific properties to the molecule, such as increased lipophilicity and potential reactivity due to the electron-withdrawing nature of the trifluoromethyl group and the electron-donating nature of the bromine atom. N-(5-bromo-2-(trifluoromethyl)phenyl)acetamide may be of interest in various chemical and pharmaceutical applications, including the synthesis of more complex molecules or as a precursor in the development of new drugs.

833-15-8

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833-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 833-15-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 833-15:
(5*8)+(4*3)+(3*3)+(2*1)+(1*5)=68
68 % 10 = 8
So 833-15-8 is a valid CAS Registry Number.

833-15-8Downstream Products

833-15-8Relevant academic research and scientific papers

Visible-light-induced Pd-catalyzed: Ortho -trifluoromethylation of acetanilides with CF3SO2Na under ambient conditions in the absence of an external photocatalyst

Zou, Long,Li, Pinhua,Wang, Bin,Wang, Lei

supporting information, p. 3737 - 3740 (2019/04/01)

A visible-light-induced Pd-catalyzed ortho-trifluoromethylation of acetanilides with CF3SO2Na was developed. The reaction proceeded smoothly at room temperature in air without any external photocatalyst or additive, providing the desired products in moderate to good yields with good functional group tolerance and regioselectivity.

Palladium-catalyzed trifluoromethylation of aromatic C-H bond directed by an acetamino group

Zhang, Li-Sheng,Chen, Kang,Chen, Guihua,Li, Bi-Jie,Luo, Shuang,Guo, Qing-Yun,Wei, Jiang-Bo,Shi, Zhang-Jie

supporting information, p. 10 - 13 (2013/04/10)

The first palladium-catalyzed ortho-trifluoromethylation of the aromatic C-H bond directed by an acetamino group is reported. This method provides an efficient and green approach to synthesize the highly biological potential key structure of ortho-CF3 acetanilides and anilines.

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