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2-(2-benzoyl-4-methylphenyl)-2-oxo-1-(p-tolyl)hydrazin-2-ium-1-ide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1456728-87-2

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1456728-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1456728-87-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,6,7,2 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1456728-87:
(9*1)+(8*4)+(7*5)+(6*6)+(5*7)+(4*2)+(3*8)+(2*8)+(1*7)=202
202 % 10 = 2
So 1456728-87-2 is a valid CAS Registry Number.

1456728-87-2Downstream Products

1456728-87-2Relevant academic research and scientific papers

Merging Visible-Light Photocatalysis and Palladium Catalysis for C-H Acylation of Azo- and Azoxybenzenes with α-Keto Acids

Xu, Ning,Li, Pinhua,Xie, Zuguang,Wang, Lei

supporting information, p. 2236 - 2242 (2016/02/12)

An efficient C-H acylation of azo- and azoxybenzenes with α-keto acids has been developed by a combination of palladium catalysis and visible-light photoredox catalysis at room temperature under 1.5 W blue LED irradiation. This method tolerates a variety of disubstituted azo- and azoxybenzenes, as well as α-keto acids regardless of the nature of the substituents. A number of aryl ketones were obtained in good yields under mild reaction conditions.

Palladium-catalyzed regio-selective oxidative C-H bond acylation of azoxybenzenes with alcohols

Hou, Lekai,Chen, Xiangxiang,Li, Shuang,Cai, Suxian,Zhao, Yanxia,Sun, Meng,Yang, Xiao-Juan

supporting information, p. 4160 - 4164 (2015/04/14)

A palladium-catalyzed regio-selective acylation of C-H bonds of azoxybenzenes with alcohols was developed using tert-butyl hydroperoxide (TBHP) as an oxidant. Alcohol derivatives can act as effective acyl precursors in situ, which are less toxic, inexpensive, stable, and commercially available. These transformations proceeded smoothly and could tolerate a variety of functional groups. This journal is

Palladium-catalyzed regioselective ortho-acylation of azoxybenzenes with aldehyde derivatives

Sun, Meng,Hou, Le-Kai,Chen, Xiang-Xiang,Yang, Xiao-Juan,Sun, Wei,Zang, Yu-Shi

supporting information, p. 3789 - 3793 (2015/02/19)

An efficient strategy for the regioselective ortho-acylation of azoxybenzenes with various aldehydes in the presence of palladium catalysts has been developed and furnishes good to excellent yields. The reaction proceeds smoothly and can tolerate a variety of functional groups.

Unprecedented ortho-acylation of azoxybenzenes with α-oxocarboxylic acids by Pd-catalyzed C-H activation and decarboxylation

Li, Hongji,Li, Pinhua,Zhao, Qiong,Wang, Lei

supporting information, p. 9170 - 9172 (2013/09/24)

A palladium-catalyzed ortho-acylation reaction of azoxybenzenes with α-oxocarboxylic acids was developed in the presence of K2S 2O8. The established methodology provides a direct approach to obtain acylated azoxybenzenes in good yields.

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