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2-phenyl-N-[4-(trifluoromethyl)phenyl]acetamide is a complex organic compound with the molecular formula C16H12F3NO. It features a phenyl group (C6H5) attached to the 2-position of an acetamide group (CH3CONH), and a 4-(trifluoromethyl)phenyl group (C6H4CF3) attached to the nitrogen atom of the acetamide. The presence of the trifluoromethyl group (CF3) imparts unique chemical and physical properties to the molecule, such as increased lipophilicity and potential for hydrogen bonding. 2-phenyl-N-[4-(trifluoromethyl)phenyl]acetamide may have applications in various fields, including pharmaceuticals, agrochemicals, and materials science, due to its specific structural features and potential interactions with biological targets.

3873-37-8

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3873-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3873-37-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3873-37:
(6*3)+(5*8)+(4*7)+(3*3)+(2*3)+(1*7)=108
108 % 10 = 8
So 3873-37-8 is a valid CAS Registry Number.

3873-37-8Downstream Products

3873-37-8Relevant academic research and scientific papers

Palladium Catalyzed Aminocarbonylation of Benzylic Ammonium Triflates with Nitroarenes: Synthesis of Phenylacetamides

Yang, Li-Miao,Li, Shan-Shan,Zhang, You-Ya,Lu, Jin-Liang,Deng, Jing-Tong,Ma, Ai-Jun,Zhang, Xiang-Zhi,Zhang, Shu-Yu,Peng, Jin-Bao

supporting information, p. 2061 - 2065 (2021/02/26)

A palladium catalyzed reductive aminocarbonylation of benzylic ammonium triflates with nitroarenes for the synthesis of phenylacetamides was developed. Using Pd(acac)2/DPPF catalyst system, a range of different substituted phenylacetamides were prepared in moderate to good yields from benzylic ammonium triflates and nitroarenes through Csp3?N bond cleavage. A variety of alkyl, aryl, and halide substituents on both substrates can be used, and many useful functional groups can be tolerated. (Figure presented.).

Compound containing bipyrazole ring, intermediate thereof and application thereof

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Paragraph 0272-0274; 0296-0298, (2020/05/14)

The invention discloses a compound containing a bipyrazole ring, and an intermediate and application thereof. The invention provides the compound containing a bipyrazole ring, as shown in a formula Iwhich is described in the specification. The compound can be used as a ligand, is high in selectivity, and is suitable for the application range of amide in C-N coupling and the C-C coupling reactionof arylboronic acid and aryl chloride, especially coupling with aryl chloride.

Preparation method of compound containing bipyrazole ring and intermediate thereof

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Paragraph 0272-0274; 0296-0299, (2020/05/14)

The invention discloses a preparation method of a compound containing a bipyrazole ring and an intermediate of the compound. The preparation method of a bipyrazole ring-containing compound as shown ina formula I comprises the following steps: (1) adding alkali into a mixture of a bipyrazole ring compound as shown in a formula I-1 and a solvent for replacement reaction to obtain a mixed system; and (2) adding an organic phosphorus compound shown as a formula I-2 into the mixed system in the step (1), and carrying out a phosphonation reaction shown in the specification, so as to obtain the bipyrazole ring-containing compound shown as the formula I, wherein R1 and R2 are independently a C1-C6 alkyl group, a C3-C8 cycloalkyl group and a phenyl group, R3 is a C1-C6 alkyl group, and X is halogen. The prepared compound containing a bipyrazole ring can be used as a ligand, and is suitable for the application range of amide in C-N coupling and the C-C coupling reaction of arylboronic acid andaryl chloride.

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