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Isoquinoline, 1-(4-methylphenyl)-, 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

494749-16-5

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494749-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 494749-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,4,7,4 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 494749-16:
(8*4)+(7*9)+(6*4)+(5*7)+(4*4)+(3*9)+(2*1)+(1*6)=205
205 % 10 = 5
So 494749-16-5 is a valid CAS Registry Number.

494749-16-5Downstream Products

494749-16-5Relevant academic research and scientific papers

Synthesis of a heptaarylisoquinoline: Unusual disconnection for constructing isoquinoline frameworks

Asako, Takashi,Suzuki, Shin,Itami, Kenichiro,Muto, Kei,Yamaguchi, Junichiro

, p. 968 - 970 (2018/08/24)

In a novel disconnection of isoquinoline ring synthesis at the C7C8/C4aC8a bonds, these bonds can be formed by a [4+2] cycloaddition between thiophene S,S-dioxide and alkynes. With a subsequent CH arylation of the resulting hexaarylisoquinoline at the C3 position, the synthesis of a fully substituted isoquinoline has been achieved.

KMnO4-mediated direct C2-selective C?H arylation of quinoline N-oxides with aromatic hydrazines

Yuan, Jin-Wei,Li, Wei-Jie,Xiao, Yong-Mei

, p. 179 - 186 (2016/12/23)

An efficient protocol for the synthesis of 2-arylquinoline N-oxides has been developed via KMnO4-mediated cross-coupling reaction of quinoline N-oxides with aromatic hydrazines in moderated to good yields. The reactions proceeded efficiently over a broad range of substrates with excellent regioselectivity and functional group tolerance.

Regioselective decarboxylative cross-coupling of carboxy isoquinoline N -oxides

Rouchet, Jean-Baptiste E. Y.,Schneider, Cédric,Fruit, Corinne,Hoarau, Christophe

, p. 5919 - 5927 (2015/06/16)

A straightforward method for direct decarboxylative arylation of 1- and 3-carboxy isoquinaldic acid N-oxides with aryl iodides is reported. The reaction proceeded selectively at the carboxy function site to exclusively give the corresponding C-1/sub

Pd-catalyzed decarboxylative cross-coupling of 2-carboxyazine N-oxides with various (hetero)aryl halides

Rouchet, Jean-Baptiste,Schneider, Cedric,Spitz, Cedric,Lefevre, Johan,Dupas, George,Fruit, Corinne,Hoarau, Christophe

supporting information, p. 3610 - 3615 (2014/04/03)

Decarboxylative cross-coupling reactions of substituted 2-carboxyazine N-oxides, with a variety of (hetero)aryl halides, by bimetallic Pd 0/CuI and Pd0/AgI catalysis are reported. Two possible pathways, a conven

Direct arylation of azine N-oxides with aryl triflates

Schipper, Derek J.,El-Salfiti, Mohamed,Whipp, Christopher J.,Fagnou, Keith

experimental part, p. 4977 - 4983 (2009/10/17)

Palladium catalyzed direct arylation of azine N-oxides using aryl triflates to afford the corresponding 2-aryl azine N-oxides is described. The reaction is carried out with a range of both N-oxides and aryl triflates. The arylation can be carried out in s

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