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N-([1,1′-biphenyl]-2-yl)-4-methylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99673-14-0

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99673-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99673-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,7 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99673-14:
(7*9)+(6*9)+(5*6)+(4*7)+(3*3)+(2*1)+(1*4)=190
190 % 10 = 0
So 99673-14-0 is a valid CAS Registry Number.

99673-14-0Relevant academic research and scientific papers

Atropisomeric Properties of N-Acyl/ N-Sulfonyl 5 H-Dibenzo[ b, d]azepin-7(6 H)-ones

Hotta, Mayuno,Makino, Kosho,Namba, Takuya,Natsugari, Hideaki,Oshitari, Tetsuta,Tabata, Hidetsugu,Takahashi, Hideyo

supporting information, p. 7563 - 7578 (2021/06/25)

The stereochemistry of N-acyl/N-sulfonyl 5H-dibenzo[b,d]azepin-7(6H)-ones (I, II) was examined in detail by freezing the conformation with a methyl group at the C-4 of dibenzoazepine. Because the two axes (axis 1, axis 2) move together concertedly, I and

Chemoselective Synthesis of N-arylbenzamides and Benzoyloxyacetanilides from Aryl Isocyanides: Styrene as Aryl and Arylcarboxymethylene Source

Sharma, Poonam,Jain, Nidhi

, p. 1932 - 1937 (2018/03/27)

Styrenes serve as unique aryl or arylcarboxymethylene source towards aryl isocyanides in the presence of Cu(II)/TBHP, and yield N-arylbenzamides or benzoyloxyacetanilides respectively. The chemoselectivity of the reaction is controlled by the nature of the substituents present on styrene ring. Whereas styrenes substituted with electron-releasing alkyl and alkoxy groups yield N-arylbenzamides, unsubstituted styrene and those with electron-withdrawing substituents furnish benzoyloxyacetanilides as the major product. With benzylamines as the substrate, N-arylbenzamides are formed exclusively as they act only as an aryl donor. TBHP serves as a promoter and oxygen source. Both the pathways are believed to proceed through an initial oxidative C?C bond cleavage of styrene. (Figure presented.).

Palladium and radical routes to phenanthridines

Bowman, W. Russell,Lyon, Jessica E.,Pritchard, Gareth J.

, p. 210 - 227 (2013/01/16)

Two routes to phenanthridines are reported; a palladium-mediated route using imidoyl-selanides as precursors and a modified radical route using aryl imines as starting materials. ARKAT-USA, Inc.

Palladium-mediated synthesis of phenanthridines: The first report of palladium insertion into imidoyl selenides

Bowman, W. Russell,Lyon, Jessica E.,Pritchard, Gareth J.

scheme or table, p. 2169 - 2171 (2009/04/08)

Imidoyl phenyl selenides have been shown to be precursors to phenanthridines, when treated with Pd(PPh3)4 under reflux in toluene in the presence of a base, giving reasonable yields. It is proposed that insertion of palladium into th

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