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2-amino-N-(2-oxoindol-3-yl)benzohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5061-17-6

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5061-17-6 Usage

Derivative of

Benzohydrazide

Functional Groups

Indole group and benzoyl group

Potential Uses

Building block in synthesis of biologically active molecules
Potential antitumor and antiproliferative agent
Potential corrosion inhibitor for mild steel in acidic media
Versatile building block in synthesis of pharmaceuticals and other chemicals

Check Digit Verification of cas no

The CAS Registry Mumber 5061-17-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5061-17:
(6*5)+(5*0)+(4*6)+(3*1)+(2*1)+(1*7)=66
66 % 10 = 6
So 5061-17-6 is a valid CAS Registry Number.

5061-17-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-N-(2-oxoindol-3-yl)benzohydrazide

1.2 Other means of identification

Product number -
Other names -

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:5061-17-6 SDS

5061-17-6Relevant academic research and scientific papers

Co(II), Ni(II), Cu(II) and Zn(II) complexes of isatinyl-2-aminobenzoylhydrazone: Synthesis, characterization and anticancer activity

Hunoor, Rekha S.,Patil, Basavaraj R.,Badiger, Dayananda S.,Chandrashekhar,Muchchandi,Gudasi, Kalagouda B.

, p. 101 - 108 (2015)

This article describes the synthesis, structural aspects and biological studies of Co(II), Ni(II), Cu(II) and Zn(II) complexes of a new hydrazone derived from the condensation of isatin and 2-aminobenzoylhydrazide. The ligand is well characterized using 1H NMR, 13C NMR, 2D HETCOR, mass and IR spectral studies. The chelating tendency of the ligand towards transition metal ions is established using analytical and spectral studies, which reveal the monobasic tridentate nature of the ligand. Octahedral geometry for Co(II), Cu(II) and Zn(II) and tetrahedral geometry for Ni(II) are tentatively proposed. All the synthesized compounds were screened for in vitro anticancer activity against Ehrlich ascites carcinoma and human cancer cell lines (adenocarcinoma HT29, kidney cancer cell line K293 and breast cancer cell line MDA231) using tryphan blue exclusion method and MTT assay.

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