Search results for "Benzyl"

showing 10 items of 878 documents

Atropine-resistant effects of the muscarinic agonists McN-A-343 and AHR 602 on cardiac performance and the release of noradrenaline from sympathetic …

1974

Abstract 1 The effects of 4-(m-chlorophenylcarbamoyloxy)-2-butynyltrimethylammonium chloride (McN-A-343) and N-benzyl-3-pyrrolidyl acetate methobromide (AHR 602) on cardiac performance and noradrenaline release from terminal sympathetic fibres were measured in isolated perfused hearts of rabbits. 2 In the presence of sufficient atropine to block muscarinic receptors, high concentrations of McN-A-343 and AHR 602 caused no cardiac stimulation and there was no increase in the resting output of noradrenaline into the perfusates. 3 McN-A-343 and AHR 602 increased both the mechanical responses and the transmitter overflow evoked by electrical stimulation of the sympathetic nerves (SNS) but inhibi…

ChronotropicAtropineMalemedicine.medical_specialtyPyrrolidinesSympathetic Nervous SystemStimulationAutopharmacologyHexamethonium CompoundsPharmacologyIn Vitro TechniquesPiperazinesHexamethonium compoundchemistry.chemical_compoundNorepinephrineCocaineInternal medicineDesipramineMuscarinic acetylcholine receptorBenzyl CompoundsmedicineAnimalsPharmacologyNeuronsHeartHydrogen-Ion ConcentrationAcetylcholineElectric StimulationPerfusionQuaternary Ammonium CompoundsAtropineEndocrinologychemistryParasympathomimeticsHexamethoniumFemaleCarbamatesRabbitsDimethylphenylpiperazinium IodideAcetylcholinemedicine.drug
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Recent Developments in Calixarenes and Their Properties

1989

The increasing number of reports, monographs and patents dealing with the hemistry of inclusion compounds shows the growing interest of organic chemists in elaborating new chemical systems presenting novel physical and chemical properties. These properties are available for fundamental as well as applied research. On the one hand, basic studies on the structure and the nature of inclusion compounds provide information on the intermolecular forces implicated in organized systems and in enzyme processes. On the other hand, applications are in progress in laboratories and industries, for instance, in catalyzing chemical reactions, in transporting and extracting metallic cations, and in modifyi…

Cone conformationMolecular levelBenzyl etherChemistryCalixareneNanotechnology
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Synthesis and characterization of a Cu(II) complex of 2-benzylmercapto-5- methyl-1,3,4-thiadiazole (C10H10N2S 2)

2008

A Cu(II) complex of 2-benzylmercapto-5-methyl-1,3,4-thiadiazole was synthesized and characterized. The crystal structure of the copper complex and the free ligand were determined by single-crystal X-ray diffraction at room temperature: {[Cu(C10H10N2S2) 2(Cl)2], P1 triclinic, a = 8.1450(2) Å, b = 8.1690(2) Å, c = 10.8180(3) Å, α = 97.4040(12)°, β = 101.6270(11)°, γ = 116.1431(14)°; C10H10N2S2 ligand, Pbca orthorhombic, a = 8.7938(7) Å, b = 9.6491(7) Å, c = 25.3552(18) Å}. The metal complex framework consists of discrete units that provide crystalline stability through a network of van der Waals contacts. The Cu(II) is coordinated by two chloride ions and two 2-benzylmercapto-5-methyl-1,3,4- …

DenticityLigandChemistryCiencias FísicasSPECTROSCOPIC BEHAVIORCrystal structureTriclinic crystal systemCU(II) COMPLEXESMagnetic susceptibilityMAGNETIC BEHAVIORCRYSTAL STRUCTUREMetal2-BENZYLMERCAPTO-5-METHYL-134-THIADIAZOLEAstronomíaCrystallographysymbols.namesakevisual_artMaterials Chemistryvisual_art.visual_art_mediumsymbolsOrthorhombic crystal systemPhysical and Theoretical Chemistryvan der Waals forceCIENCIAS NATURALES Y EXACTAS
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A rapid and sensitive gas chromatography-mass spectrometry method for the quality control of perfumes: simultaneous determination of phthalates

2013

A rapid and sensitive analytical gas chromatography-mass spectrometry (GC-MS) method for perfume analysis to determine the phthalates banned by the European Union Regulation on cosmetic samples is presented. This method has been tested in commercial alcoholic perfume samples for the determination of the following seven phthalates: dibutyl phthalate, bis(2-ethylhexyl) phthalate, bis(2-methoxyethyl) phthalate, n-pentyl-isopentylphthalate, di-n-pentyl phthalate, diisopentylphthalate and benzyl butyl phthalate. Sample evaporation and redissolution in ethanol is carried out before GC-MS analysis, with no dilution of the sample. External calibration and standard addition calibration are compared …

Detection limitChromatographyDibutyl phthalateGeneral Chemical EngineeringGeneral EngineeringPhthalateRepeatabilityAnalytical Chemistrychemistry.chemical_compoundchemistryBenzyl butyl phthalateStandard additionmedia_common.cataloged_instanceEuropean unionGas chromatography–mass spectrometrymedia_commonAnal. Methods
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CCDC 210702: Experimental Crystal Structure Determination

2003

Related Article: C.Capacchione, A.Proto, H.Ebeling, R.Mulhaupt, K.Moller, T.P.Spaniol, J.Okuda|2003|J.Am.Chem.Soc.|125|4964|doi:10.1021/ja029968g

Dibenzyl-(14-dithiabutane-14-diyl-22'-bis(46-di-t-butyl-phenolato))-hafnium pentane solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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ChemInform Abstract: Reaction of 2,2′-Bis(N-methylindolyl) with Dimethyl Acetylenedicarboxylate and Thermally and Photochemically Induced Cyclization…

2010

2,2′-Bis(N-methylindolyl) 1 reacts with dimethyl acetylenedicarboxylate to furnish the 3-dimethyl maleoyl-substituted 2,2′-bisindolyl 2. Compound 2 cyclizes under aluminum trichloride catalysis according to a polar process to give a cyclopenta[2,1-b:3,4-b′]diindole derivative 4. Reaction of compound 4 with benzyl-amine yields the spiro derivative 5. Photochemically-induced 1,6-electrocyclization of compound 2 gives rise to the indolo[2,3-a]carbazole 6 directly, which is readily transformed to the pyrrolo-annelated carbazole 7 by treatment with benzylamine.

Dimethyl acetylenedicarboxylatechemistry.chemical_compoundBenzylaminechemistryCarbazoleAluminum trichlorideGeneral MedicineMedicinal chemistryDerivative (chemistry)CatalysisChemInform
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Reaction of 2,2′-bis(N-methylindolyl) with dimethyl acetylenedicarboxylate and thermally- and photochemically-induced cyclizations of the product

1995

2,2′-Bis(N-methylindolyl) 1 reacts with dimethyl acetylenedicarboxylate to furnish the 3-dimethyl maleoyl-substituted 2,2′-bisindolyl 2. Compound 2 cyclizes under aluminum trichloride catalysis according to a polar process to give a cyclopenta[2,1-b:3,4-b′]diindole derivative 4. Reaction of compound 4 with benzyl-amine yields the spiro derivative 5. Photochemically-induced 1,6-electrocyclization of compound 2 gives rise to the indolo[2,3-a]carbazole 6 directly, which is readily transformed to the pyrrolo-annelated carbazole 7 by treatment with benzylamine.

Dimethyl acetylenedicarboxylatechemistry.chemical_compoundBenzylaminechemistryCarbazoleAluminum trichlorideOrganic ChemistryOrganic chemistryMedicinal chemistryDerivative (chemistry)CatalysisJournal of Heterocyclic Chemistry
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CCDC 795076: Experimental Crystal Structure Determination

2011

Related Article: M.Muller, M.Albrecht, J.Sackmann, A.Hoffmann, F.Dierkes, A.Valkonen, K.Rissanen|2010|Dalton Trans.|39|11329|doi:10.1039/c0dt00766h

Dimethyl(pentafluorobenzyl)phenylphosphonium bromide hemihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 261837: Experimental Crystal Structure Determination

2006

Related Article: S.Busi, M.Lahtinen, M.Karna, J.Valkonen, E.Kolehmainen, K.Rissanen|2006|J.Mol.Struct.|787|18|doi:10.1016/j.molstruc.2005.10.027

Dimethyl-bis(3-methylbenzyl)ammonium chloride monohydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Understanding the Solution Behavior of Epinephrine in the Presence of Toxic Cations: A Thermodynamic Investigation in Different Experimental Conditio…

2020

The interactions of epinephrine ((R)-(&minus

EnthalpyInorganic chemistryPharmaceutical ScienceIonic bondingProtonation02 engineering and technologyCalorimetry010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug Discoverytoxic cationSettore CHIM/01 - Chimica Analiticatoxic cationsepinephrinePhysical and Theoretical ChemistryChemistryOrganic Chemistryenthalpy and entropy changesOxidesMethylmercury Compoundsdependence on ionic strength021001 nanoscience & nanotechnologysequestering ability0104 chemical sciencesSpecific ion interaction theoryChemistry (miscellaneous)Ionic strengthBenzyl alcoholThermodynamicsUraniumMolecular MedicineTitration0210 nano-technologyenthalpy and entropy changeMolecules
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