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Ethanediamide, N,N'-bis(2-aminophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88116-37-4

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88116-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88116-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,1 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88116-37:
(7*8)+(6*8)+(5*1)+(4*1)+(3*6)+(2*3)+(1*7)=144
144 % 10 = 4
So 88116-37-4 is a valid CAS Registry Number.

88116-37-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis(2-aminophenyl)oxamide

1.2 Other means of identification

Product number -
Other names 2,2'-diaminooxanilide

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:88116-37-4 SDS

88116-37-4Downstream Products

88116-37-4Relevant academic research and scientific papers

Synthesis and structure of large 24-mer and 36-mer oxamate-based macrocycles

Weheabby, Saddam,Abdulmalic, Mohammad A.,Kataev, Evgeny A.,Shumilova, Tatiana A.,Rüffer, Tobias

, p. 461 - 474 (2017)

Poly(cyclic) oxamates represent novel and potentially multidentate ligands for coordination chemistry. To obtain them, the treatment of 2-nitroaniline with two equivalents of oxalyl chloride afforded N,N'-bis(2-nitrophenyl)oxalamide (1), and by reduction

Synthesis of novel acyclic and multiple phenyl iron tetraamino ligand catalysts and its catalytic activity for degradation of dye wastewater by H2O2

Li, Shun-Lai,Zhou, Run,Zhao, Wei-Jing,Du, Hong-Guang

, (2021/05/07)

We need a practical, inexpensive, and green way to reduce the environmental pollutants, especially for dye wastewater. The discharge of industrial wastewater such as organic dyes will cause serious pollution to water bodies, thereby affecting people's liv

Bis phenylene flattened 13-membered tetraamide macrocyclic ligand (TAML) for square planar cobalt(III)*

Ellis, W. Chadwick,Ryabov, Alexander D.,Fischer, Andreas,Hayden, Joshua A.,Shen, Longzhu Q.,Bominaar, Emile L.,Hendrich, Michael P.,Collins, Terrence J.

, p. 1822 - 1836 (2018/07/03)

The preparation, characterization, and evaluation of a cobalt(III) complex (Figure presented.) with 13-membered tetraamide macrocyclic ligand (TAML) is described. This is a square-planar (X-ray) S?=?1 paramagnetic (1H NMR) compound, which becomes an S?=?0 diamagnetic octahedral species in excess d5-pyridine. Its one-electron oxidation at an electrode is fully reversible with the lowest E? value (0.66?V vs SCE) among all investigated CoIII TAML complexes. The oxidation results in a neutral blue species which is consistent with a CoIII/radical-cation ligand. The ease of oxidation is likely due to the two benzene rings incorporated in the ligand structure (whereas there is just one in many other CoIII TAMLs). The oxidized neutral species are unexpectedly EPR silent, presumably due to the π-stacking aggregation. However, they display eight-line hyperfine patterns in the presence of excess of 4-tert-butylpyridine or 4-tert-butyl isonitrile. The EPR spectra are more consistent with the CoIII/radical-cation ligand formulation rather than with a CoIV complex. Attempts to synthesize a similar vanadium complex under the same conditions as for cobalt using [VVO(OCHMe2)3] were not successful. TAML-free decavanadate was isolated instead.

Metal Template Reactions. XVI. Design and Synthesis of Primary Diamine Ligands with Additional Nitrogen Donor Atoms

Black, David St. C.,Rothnie, Neil E.

, p. 1141 - 1147 (2007/10/02)

Five new primary diamines (8), (10), (12), (20) and (22) have been synthesized.These compounds contain additional nitrogen donor atoms suitable for metal chelation.An improved preparation of the triamine (6) is also reported.

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