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N-phenylbenzohydrazide is an organic compound with the chemical formula C13H11N2O. It is a derivative of benzoic acid, where the hydroxyl group is replaced by a phenylhydrazine group. This white crystalline solid is used as a reagent in chemical analysis, particularly for the detection and determination of aldehydes and ketones. It forms a yellow precipitate with aldehydes, which is useful for qualitative analysis. Additionally, N-phenylbenzohydrazide has been studied for its potential applications in the synthesis of pharmaceuticals and as a building block in the creation of more complex organic molecules.

579-45-3

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579-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 579-45-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 579-45:
(5*5)+(4*7)+(3*9)+(2*4)+(1*5)=93
93 % 10 = 3
So 579-45-3 is a valid CAS Registry Number.

579-45-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenylbenzohydrazide

1.2 Other means of identification

Product number -
Other names benzoyl phenylhydrazine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:579-45-3 SDS

579-45-3Relevant academic research and scientific papers

Four Simultaneously Dynamic Covalent Reactions. Experimental Proof of Orthogonality

Seifert, Helen M.,Ramirez Trejo, Karina,Anslyn, Eric V.

supporting information, p. 10916 - 10924 (2016/09/09)

Dynamic covalent reactions are widely used in dynamic combinatorial chemistry. Most of these reactions are run under differing reaction conditions and exhibit cross-reactivity when components of multiple reactions are present in one reaction vessel. Herei

Syntheses and antitumor activities of N′1, N′3-dialkyl-N′1,N′3-di- (alkylcarbonothioyl) malonohydrazide: The discovery of elesclomol

Chen, Shoujun,Sun, Lijun,Koya, Keizo,Tatsuta, Noriaki,Xia, Zhiqiang,Korbut, Timothy,Du, Zhenjian,Wu, Jim,Liang, Guiqing,Jiang, Jun,Ono, Mitsunori,Zhou, Dan,Sonderfan, Andrew

, p. 5070 - 5076 (2013/09/12)

A series of N′1,N′3-dialkyl- N′1,N′3-di(alkylcarbonothioyl) malonohydrazides have been designed and synthesized as anticancer agents by targeting oxidative stress and Hsp70 induction. Structure-activity relationship (SAR) studies lead to the discovery of STA-4783 (elesclomol), a novel small molecule that has been evaluated in a number of clinical trials as an anticancer agent in combination with Taxol.

Photoinduced cleavage of N-N bonds of aromatic hydrazines and hydrazides by visible light

Zhu, Mingzhao,Zheng, Nan

supporting information; experimental part, p. 2223 - 2236 (2011/09/15)

A photocatalytic system involving [Ru(bpyrz)(PFH, visible light, and air has been developed for cleavage of the N-N bonds of hydrazines and hydrazides. This catalytic system is generally effective for N,N-disubstituted hydrazine and hydrazide derivatives, including arylhydrazides, N-alkyl-N-arylhydrazines, and N,N-diarylhydrazines. The utility of this cleavage reaction has been demonstrated by synthesizing a variety of secondary aromatic amines. Georg Thieme Verlag Stuttgart ? New York.

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