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N-(4′-methyl[1,1′-biphenyl]-2-yl)benzamide is a complex organic compound with the chemical formula C19H17NO. It is a derivative of benzamide, featuring a biphenyl group with a methyl substitution at the 4' position and an amide functional group. N-(4′-methyl[1,1′-biphenyl]-2-yl)benzamide is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique structure and properties. It is characterized by its ability to form stable molecules and may be involved in chemical reactions that are relevant to the synthesis of certain drugs or other chemical products. The specific uses and effects of N-(4′-methyl[1,1′-biphenyl]-2-yl)benzamide are subject to ongoing research and may vary depending on the context in which it is applied.

1233-27-8

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1233-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1233-27-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1233-27:
(6*1)+(5*2)+(4*3)+(3*3)+(2*2)+(1*7)=48
48 % 10 = 8
So 1233-27-8 is a valid CAS Registry Number.

1233-27-8Relevant academic research and scientific papers

Unified Protocol for Cobalt-Catalyzed Oxidative Assembly of Two Aryl Metal Reagents Using Oxygen as an Oxidant

Liao, Lian-Yan,Liu, Kun-Ming,Duan, Xin-Fang

, p. 9856 - 9867 (2015/11/03)

The first cobalt-catalyzed oxidative cross-coupling reaction of two aryl metal reagents is described. An equivalent amount of two aryl Grignard or lithium reagents, after mediation by an equivalent amount of simple ClTi(OEt)3, was facilely assembled under the catalysis of 1 mol % of CoCl2/10 mol % of DMPU using oxygen. The cross-couplings between various aryl metal reagents, especially between two structurally similar aryl Grignard reagents, proceeded smoothly and selectively and, thus, provided a highly general and efficient method for the construction of biaryl compounds.

Application of Semmler-Wolff Reaction for the Synthesis of 2-Aminobiphenyls

Sivasubramanian, S.,Muthusubramanian, S.,Ramasamy, S.,Arumugam, N

, p. 552 - 554 (2007/10/02)

Semmler-Wolff reaction of 1-hydroxyimino-2-aryl-2-cyclohexenes (I) yields the corresponding 2-aminobiphenyls (II) in 40-55percent yield.The 2-aminobiphenyls have been fully characterized through spectral data.Further confirmation of the structures of 2-aminobiphenyls is obtained by their conversion to the corresponding phenanthridine derivatives (IV).

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