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Benzoic acid, 2-acetyl-2-phenylhydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23459-55-4

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23459-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23459-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,5 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23459-55:
(7*2)+(6*3)+(5*4)+(4*5)+(3*9)+(2*5)+(1*5)=114
114 % 10 = 4
So 23459-55-4 is a valid CAS Registry Number.

23459-55-4Downstream Products

23459-55-4Relevant academic research and scientific papers

Ligand-free Cu(ii)-mediated aerobic oxidations of aldehyde hydrazones leading to N,N′-diacylhydrazines and 1,3,4-oxadiazoles

Liu, Lei,Feng, Suliu

supporting information, p. 2585 - 2592 (2017/04/03)

A Cu(ii)-mediated synthesis of N,N′-diacylhydrazines and 1,3,4-oxadiazoles from aldehyde hydrazones has been developed. This is the first time that the synthesis of N,N′-diacylhydrazines and 1,3,4-oxadiazoles using N,N-dimethylamides as the acylation reagent and O2 in air as the oxidation reagent is reported. These reactions offered several advantages including simple workups, ligand-free inexpensive metal salts as mediators, high yields, and wide scope of substrates.

Hypervalent iodine (III)-mediated oxidation of aryl sulfonylhydrazones: A facile synthesis of N-aroyl-N′-acyl arylsulfonylhydrazides

Ramakrishna,Dev, Kapil,Maurya, Saransh Wales,Siddiqui, Ibadur Rahman,Maurya, Rakesh

supporting information, p. 570 - 573 (2017/01/16)

We have developed a novel and efficient method for the oxidation of aryl sulfonylhydrazones to N-aroyl-N′-acyl arylsulfonylhydrazides, using hypervalent iodine (III) reagent in good yields at room temperature.

Acylation Reactions of Phenylhydrazines. Preparation and Properties of New Diacylphenylhydrazines

Hearn, Michael J.,Magee, Debra J.,Alhart, Randi,Gleva, Marye,Goldstein, Susan,et al.

, p. 129 - 131 (2007/10/02)

Anhydride acylation reactions of a variety of substituted arylhydrazines under mild conditions led to controlled formation of the acid phenylhydrazides I (Table I).The procedures were tallored to the particular state of the starting arylhydrazine.Second-s

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