Search results for "Aniline"

showing 10 items of 259 documents

Acute lethal toxicity of some pesticides toBrachionus calyciflorus andBrachionus plicatilis

1991

Due to their widespread distribution and toxic nattwe pesticides may have a serious impact on the aquatic environment and exert adverse effects on the associated organisms. Acute bioassay tests have been used to determine the actual impact of various pesticides on aquatic life. Static acute toxicity tests provide rapid and reproductible concentration-response curves for estimating toxic effects of chemicals on aquatic organisms. These tests provide a data base for determining relative toxicity to a variety of species.

Health Toxicology and MutagenesisRotiferaFresh WaterBiologyToxicologyLethal Dose 50ToxicologySpecies SpecificityBrachionus calyciflorusAnimalsEcotoxicologyBioassaySeawaterPesticidesTrichlorfonAniline CompoundsEcologyAquatic ecosystemFenitrothionGeneral MedicinePesticideBrachionusbiology.organism_classificationPollutionAcute toxicityToxicityChlorpyrifosHexachlorocyclohexaneBulletin of Environmental Contamination and Toxicology
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Partition Behavior of Anilines in Bulk‐Phase and High‐Performance Liquid Chromatographic Systems: Influence on Correlation with Biological Constants

1992

Abstract The partition behavior of a mixed series of ring‐substituted anilines in reversed‐phase high‐performance liquid chromatographic systems is substantially different from that observed in a classical bulk‐phase partition system with n ‐heptane as the aprotic reference solvent. On the basis of the equivalence of each ring substituent in the p ‐straight‐chain methylene groups (ν value) as a function of the fraction of organic solvent (acetonitrile or methanol) in the mobile phase, the biased partition behavior for imperfect homologues and heterologues is verified relative to that of perfect homologues. This behavior was tentatively attributed, mainly, to differences in the hydrogen bond…

HeptaneAcetonitrilesAniline CompoundsChromatographyChemistryMethanolSubstituentAnalytical chemistryPharmaceutical ScienceIntestinal absorptionSolventPartition coefficientchemistry.chemical_compoundReaction rate constantPartition (number theory)AcetonitrileChromatography High Pressure LiquidJournal of Pharmaceutical Sciences
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Monitoring the hydrogen bond net configuration and the dimensionality of aniline and phenyloxamate by adding 1 H -pyrazole and isoxazole as substitue…

2019

This work describes the synthesis and characterization of a new class of oxamic acid derivatives containing pyrazole and isoxazole as substituents to investigate their ability to form hydrogen bonds aiming at applying them in crystal engineering and molecular self-recognition. In this respect, we report a new synthesis of 2-(4-nitrophenyl)-1,3-propanedial (1) in high yield using SOCl2 as a chlorinating agent. The new oxamic esters 4-(1H-pyrazol-4-yl)phenylene-N-(ethyloxamate) (2d) and 4-(1,2-oxazol-4-yl)phenylene-N-(ethyloxamate) (3d) were prepared from 1. The synthetic route consists of the cyclisation of 1 either with hydrazine to afford 4-(-aminophenyl)-1H-pyrazole (2a) or with hydroxyla…

Hydrogen bond02 engineering and technologyGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryPyrazole[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsCrystal engineering01 natural sciencesMedicinal chemistry0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundAnilinechemistryPalladium on carbonMoleculeHydroxideGeneral Materials Science[CHIM.COOR]Chemical Sciences/Coordination chemistryIsoxazole0210 nano-technologyComputingMilieux_MISCELLANEOUS
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15N NMR: Substituent effect analysis inpara-andmeta-substituted phenylhydrazines

1994

15N NMR spectra of phenylhydrazine and of 14 para- and meta-substituted phenylhydrazines were measured at natural isotope abundance in DMSO-d6 solution. The substituent present exerts a larger influence on the chemical shift of the nitrogen atom directly bound to the aromatic ring (N-1) than on the second one (N-2), which shows an attenuated and inverted trend. The chemical shifts of N-1 and N-2 give a good cross correlation in both series of compounds if p-NO2 and m-F derivatives are excluded from the correlations of para- and meta-substituted phenylhydrazines, respectively. Moreover, N-1 SCS values show good linear correlations with Hammett substituent constants, with SCSs of directly bou…

HydrogenStereochemistryChemical shiftPhenylhydrazinesSubstituentchemistry.chemical_elementGeneral ChemistryRing (chemistry)Medicinal chemistryNMR spectra databasechemistry.chemical_compoundAnilinechemistryGeneral Materials SciencePhenylhydrazineMagnetic Resonance in Chemistry
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Direct involvement of acid centers of polyaniline in charge transfer on organic acceptor

1996

Abstract Electrochemical behavior of hydroquinone and 4F-hydroquinone has been studied on Pt/polyaniline (PANI) electrodes in 1 M H 2 SO 4 solution. Redox transformation of quinone/hydroquinone systems takes place on PANI practically without overpotential and, probably, the two-electron charge transfer processes are realized in such systems. Reaction currents depend on PANI quantities deposited on the Pt electrode and the molecular complex is formed. There exists a great electronic exchange between acid centers of PANI and quinone/hydroquinone molecules, resulting in electronic conjugation of this surface state (adsorbed molecule) with the polymer. Existence of such complexes was confirmed …

HydroquinoneMechanical EngineeringInorganic chemistryMetals and AlloysOverpotentialCondensed Matter PhysicsElectrochemistryAcceptorRedoxElectronic Optical and Magnetic MaterialsQuinonechemistry.chemical_compoundchemistryMechanics of MaterialsPolyanilineMaterials ChemistryMoleculeSynthetic Metals
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Design and synthesis of 1-aryl-5-anilinoindazoles as c-Jun N-terminal kinase inhibitors.

2012

Starting from pyrazole HTS hit (1), a series of 1-aryl-1H-indazoles have been synthesized as JNK3 inhibitors with moderate selectivity against JNK1. SAR studies led to the synthesis of 5r as double digital nanomolar JNK3 inhibitor with good in vivo exposure.

IndazolesStereochemistryClinical BiochemistryPharmaceutical SciencePlasma protein bindingPyrazoleBiochemistrychemistry.chemical_compoundStructure-Activity RelationshipIn vivoMitogen-Activated Protein Kinase 10Drug DiscoveryStructure–activity relationshipAnimalsMitogen-Activated Protein Kinase 8Molecular BiologyProtein Kinase InhibitorsAniline CompoundsChemistryKinaseArylOrganic Chemistryc-junJNK Mitogen-Activated Protein KinasesBrainCombinatorial chemistryRatsDrug DesignMolecular MedicineSelectivityHalf-LifeProtein BindingBioorganicmedicinal chemistry letters
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Infracyanine Green vs. Brilliant Blue G in Inverted Flap Surgery for Large Macular Holes: A Long-Term Swept-Source OCT Analysis

2020

Background and Objectives: To compare the long-term toxicity of infracyanine green (IFCG) to brilliant blue G (BBG) in inverted internal limiting membrane flap surgery (I-ILMFS) for large, full-thickness macular holes (FTMHs). Materials and Methods: Prospective randomized study including 39 eyes with &ge

Indocyanine GreenMalemedicine.medical_specialtyDistance visual acuitygenetic structuresswept-source OCTlarge macular holeNerve fiber layerContrast MediaInfracyanine greenRetinaSurgical FlapsArticlechemistry.chemical_compoundRosaniline DyesmedicineHumansExternal limiting membranebrilliant blue GAgedAged 80 and overlcsh:R5-920inverted flap surgerySettore MED/30 - Malattie Apparato Visivobusiness.industryInternal limiting membraneRetinalGeneral MedicineMiddle AgedRetinal Perforationseye diseasesSurgeryGanglionTreatment Outcomemedicine.anatomical_structureInfracyanine greenchemistryFemalebusinesslcsh:Medicine (General)Infracyanine green; brilliant blue G; inverted flap surgery; large macular hole; swept-source OCTTomography Optical CoherenceBrilliant blue GMedicina
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Molecular structure and electric properties of N -methyl- N -nitroaniline and its derivatives

2001

A comparative study of the molecular structure of N-methyl-N-nitroaniline and its derivatives is carried out employing the Kerr effect and dipole moments methods in combination with the crystallographic analysis. The obtained experimental structural data agree with the quantum-chemical calculations by the B3LYP/6-31G p and MP2/3-21G p methods. The measurement and calculation results are used to draw conclusions about the mutual interaction and role of various substituents to the Nmethyl-N-nitroaniline molecule. q 2001 Elsevier Science B.V. All rights reserved.

Inorganic ChemistryDipoleKerr effectKerr constantChemistryComputational chemistryOrganic ChemistryElectric propertiesPhysical chemistryMoleculeSpectroscopyAnalytical ChemistryNitroanilineJournal of Molecular Structure
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Formation of the Cationic [(2‐Aminoethenyl)carbine]iron Complexes by Treatment of (2‐Methoxyethenyl)carbene Complexes with Primary Amines:Synthesis a…

1997

Cationic (2-methoxyethenyl)methoxycarbene iron complexes 2, [Cp(CO)2Fe(C(OMe)CHCR(OMe))+][PF6−], are obtained by the addition of methanol to the corresponding (alkynyl)-methoxycarbene complexes 1, [Cp(CO)2Fe(C(OMe)CCR)+][PF6−]. Primary amines, H2NR', react with these 1,3-dimethoxy-substituted (alkenyl)carbene complexes, 2, through an addition/elimination process to yield cationic (2-aminoethenyl)methoxycarbene iron complexes, 3, [Cp(CO)2Fe(C(OMe)CHCR(NHR'))+][PF6−] in an isolated yield of 71–90%. The complexes 3a–c were characterized by X-ray structural analyses. Thus, previously isolated products, from the reaction, of the (alkynyl)methoxycarbene complexes 1a and 1c, with aniline at room t…

Inorganic Chemistrychemistry.chemical_compoundPrimary (chemistry)AminolysisAnilinechemistryYield (chemistry)Cationic polymerizationOrganic chemistryCarbineMethanolMedicinal chemistryCarbeneChemische Berichte
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Oxygen atom transfer reaction involving oxomolybdenum complexes with sterically bulky thiocarboxylate ligands and biochemical interesting substrates …

1999

Abstract Oxidation–reduction reactions of substrates in systems containing the complex [Mo VI O 2 (O 2 CC(S)CH 3 Ph) 2 ] 2− in methanol have been investigated as models of oxo-transfer reactions. At neutral pH, the [Mo VI O 2 (O 2 CC(S)CH 3 Ph) 2 ] 2− reacts with Me 2 PhP or n -butanethiol to yield a [Mo IV O(O 2 CC(S)CH 3 Ph) 2 ] 2− species and Me 2 PhPO or disulfide, respectively. The Mo IV O complex reduces a variety of substrates XO = Me 2 SO and pyridine N-oxide conducing formation of X = Me 2 S and pyridine. The occurrence of these reactions produces a catalytic system Me 2 PhP + XO → Me 2 PhPO + X and 2BuSH + XO → [BuS] 2  + X + H 2 O. In this work we have also included the study of …

Inorganic chemistryMedicinal chemistryCatalysisInorganic ChemistryNitrobenzenechemistry.chemical_compoundAnilinechemistryBenzoinPyridineMaterials ChemistryMethanolBenzilPhysical and Theoretical ChemistryButanethiolInorganica Chimica Acta
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