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2-Pyridinecarboxamide, N-(2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90209-82-8

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90209-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90209-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,0 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90209-82:
(7*9)+(6*0)+(5*2)+(4*0)+(3*9)+(2*8)+(1*2)=118
118 % 10 = 8
So 90209-82-8 is a valid CAS Registry Number.

90209-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-nitrophenyl)pyridine-2-carboxamide

1.2 Other means of identification

Product number -
Other names Pyridine-2-carboxylic acid,(2-nitro-phenyl)-amide

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:90209-82-8 SDS

90209-82-8Relevant academic research and scientific papers

Sodium persulfate-promoted site-selective synthesis of mononitroarylamines under transition-metal-free conditions

Xie, De-Xun,Yu, Hui-Juan,Liu, Hui,Xue, Wei-Cai,Qin, Yuan-Shou,Shao, Guang

, p. 1157 - 1165 (2019/01/24)

A practical preparation of nitroarylamines from protected arylamines was herein disclosed. In this system, sodium nitrite acted as a nitration reagent in the presence of sodium persulfate without any transition-metal catalysts. This efficient site-selective protocol took place at room temperature for a short time through a free radical pathway.

Investigation of dioxygen activation by copper(ii)-iminate/aminate complexes

Papanikolaou, Michael G.,Hadjithoma, Sofia,Chatzikypraiou, Dimitra S.,Papaioannou, Dionysios,Drouza, Chryssoula,Tsipis, Athanassios C.,Miras, Haralampos N.,Keramidas, Anastasios D.,Kabanos, Themistoklis A.

, p. 16242 - 16254 (2018/11/30)

The activation of dioxygen by metal ions is critical in chemical and bio-chemical processes. A scientific challenge is the elucidation of the activation site of dioxygen in some copper metalloproteins, which is either the metal center or the substrate. In an effort to address this challenge, we prepared a series of new copper(ii) complexes (1·2H2O, 2·CH3OH, 3) with bio-inspired amidate ligands and investigated their activity towards dioxygen activation. The secondary amine group ligated to copper(ii) of the complex 1·2H2O in methyl alcohol is oxidized (2e?) by air dioxygen in a stepwise fashion to an imine group, affording complex 2. The copper(ii) complex 2 in methyl alcohol induces the 4e? oxidation by air dioxygen of the imine functionality ligated to copper(ii) to an azinate group, resulting in the isolation of a dinuclear azinate copper(ii) compound (4). Experimental and computational studies, including X-band c. w. EPR, UV-vis and ESI-MS spectroscopy and density functional theory computations, indicate a direct attack of the dioxygen on the-HC═N-group ligated to copper(ii), and a possible mechanism of the oxidation of the-HC═N-functionality ligated to copper(ii) to an azinate group is provided. This unprecedented activation of dioxygen by a copper substrate paves the way for further exploration of the O2 activation mechanisms in enzymes and the development of effective catalysts in O2-involved green organic synthesis.

Membrane-permeable Mn(III) complexes for molecular magnetic resonance imaging of intracellular targets

Barandov, Ali,Bartelle, Benjamin B.,Gonzalez, Beatriz A.,White, William L.,Lippard, Stephen J.,Jasanoff, Alan

supporting information, p. 5483 - 5486 (2016/06/01)

Intracellular compartments make up roughly two-thirds of the body, but delivery of molecular imaging probes to these spaces can be challenging. This situation is particularly true for probes designed for detection by magnetic resonance imaging (MRI), a hi

Liposome-based gene delivery systems containing a steroid derivative: computational and small angle X-ray diffraction study

Galeazzi,Bruni,Crucianelli,Laudadio,Marini,Massaccesi,Mobbili,Pisani

, p. 54070 - 54078 (2015/07/01)

In this study, the structural properties and the phase behaviour of mixed composition neutral liposomes containing a functionalized steroid are reported. With the aim to design neutral liposomes able to coordinate cations and to complex DNA, we synthesized cholesteryl-2-(picolinamido)-phenylcarbamate (CHOLp) containing an N-aryl picolinamide group as chelating agent linked to the steroid structure via a carbamate moiety. The phase behaviour of mixtures of the functionalized cholesterol (CHOLp) and dioleoyl-phosphatidylcholine (DOPC) was investigated by means of X-ray diffraction. Simultaneously, atomistic molecular dynamics simulations of DOPC/CHOLp bilayers as a function of CHOLp molar fractions were carried out to investigate the specific effects of the polar steroid on the structural and dynamic properties of these zwitterionic bilayers. The molecular modelling studies have been performed both in absence and in presence of bivalent cations salts in order to assess the CHOLp ability to coordinate metal ions. The results show good stability of the resulting DOPC/CHOLp bilayers which is improved by the presence of salt. This is particularly evident at low amount of CHOLp where a high order of the lipid tails can be observed, suggesting stabilization of the corresponding DOPC liposomes. This feature can be ascribed to the polar nature and structural properties of the ligand. In fact, due to the presence of the aromatic moieties, CHOLp combines two different behaviours, namely a propensity to realize both intermolecular π-stacking interactions and cation-π bonding mainly evident in CaCl2. The last feature confirms for CHOLp a role as a cation-mediated complexation agent for DNA. The X-ray diffraction data on the capability of DOPC/CHOLp liposomes to complex DNA was also reported.

Amide linkage isomerism as an activity switch for organometallic osmium and ruthenium anticancer complexes

Van Rijt, Sabine H.,Hebden, Andrew J.,Amaresekera, Thakshila,Deeth, Robert J.,Clarkson, Guy J.,Parsons, Simon,McGowan, Patrick C.,Sadler, Peter J.

supporting information; experimental part, p. 7753 - 7764 (2010/04/24)

We show that the binding mode adopted by picolinamide derivatives in organometallic OsII and RuII half-sandwich complexes can lead to contrasting cancer cell cytotoxicity. N-Phenyl picolinamide derivatives (XY) in OsII (1, 3-5, 7, 9) and RuII (2, 6, 8, 10

Comparative Mass Spectral Study of 2-Aza and 2'-Azabenzanilides and Their Thio Anlogues

Ramana, D. V.,Krishna, N. V. S. Rama

, p. 517 - 521 (2007/10/02)

Intramolecular aromatic substitution reactions involving nitrogen of the pyridine ring and sulfur have been observed in 2-aza- and 2'-azathiobenzanilides under electron impact while expelling the hydrogen or the ortho substituent from the molecular ions of these compounds.Hydrogen migration from nitrogen to the sulfur leads to the + ion while the migration of aryl group to sulfur affords +.Interesting ortho interactions of methoxy and the methyl substituents have also been noticed in 2-methoxy-2'-azathiobenzanilide and 2'-methyl-2-azathiobenzanilide in enhancing the relative abundance of +.But the mass spectra of the corresponding oxygen analogues contain peaks chiefly due to simple cleavages resulting in abundant benzoyl cations.

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