Search results for "Dimethylamine"

showing 10 items of 34 documents

In vivo antigenotoxic effects of dietary allyl sulfides in the rat

1997

The effects of dietary administration of diallyl sulfide (DAS), diallyl disulfide (DADS) and allyl mercaptan (AM) on the genotoxicity of different chemicals were studied in two experimental systems: (i) measurement of hepatic DNA single-strand breaks induced in rats by aflatoxin B1 (AFB1), N-nitrosodimethylamine (NDMA) or methylnitrosourea (MNU); (ii) mutagenicity of AFB1 or NDMA on Salmonella typhimurium TA100 using hepatic S9 from rats fed allyl sulfides as the activation system. All compounds strongly reduced hepatic DNA breaks induced by AFB1 and NDMA but did not modify the genotoxicity of MNU. In the Ames test, the mutagenicity of NDMA was strongly inhibited by hepatic S9 from rats fed…

MaleSalmonella typhimuriumCancer ResearchAflatoxin B1[SDV]Life Sciences [q-bio]Allyl compoundMutagenSulfidesmedicine.disease_cause030226 pharmacology & pharmacyDimethylnitrosamineAmes test03 medical and health scienceschemistry.chemical_compound0302 clinical medicineN-NitrosodimethylaminemedicineAnimalsAnticarcinogenic AgentsDisulfidesComputingMilieux_MISCELLANEOUSMutagenicity TestsDiallyl disulfidefood and beveragesAntimutagenic AgentsMethylnitrosoureaRats3. Good healthAllyl Compounds[SDV] Life Sciences [q-bio]LiverOncologychemistryBiochemistry030220 oncology & carcinogenesisRATAllyl MercaptanCARCINOGENESEAllyl SulfideGenotoxicityDNA DamageMutagensCancer Letters
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Controllable coverage of chemically modified graphene sheets with gold nanoparticles by thermal treatment of graphite oxide with N,N-dimethylformamide

2013

Abstract We describe a simple chemical method to reduce and functionalize graphite oxide by reaction with dimethylformamide under controlled heating. Our experiments suggest that the reaction conditions assist the decomposition of the solvent to produce dimethylamine molecules that can react with the oxygen-rich functional groups covering the surface of the exfoliated layers of graphene, therefore generating chemically modified graphene (CMG). These N-functionalities have been next used as anchoring points for the grafting of Au nanoparticles. Given that the functionalization extent can be controlled with the temperature and reaction time, our approach can be considered as a straightforward…

Materials scienceGraphenefood and beveragesNanoparticleNanotechnologyGraphite oxide02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundchemistryChemical engineeringlawColloidal goldDimethylformamideSurface modificationGeneral Materials Science0210 nano-technologyDimethylamineGraphene oxide paperCarbon
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On the reaction of some 5-polyfluoroaryl-1,2,4-oxadiazoles with methylhydrazine: synthesis of fluorinated indazoles

2009

The reaction of 5-polyfluoroaryl-1,2,4-oxadiazoles with methylhydrazine has been studied and the synthesis of fluorinated N-methylindazoles has been realized. Rearrangement reactions showed predominantly formation of N(1)-methylindazole regioisomers. Starting compounds were preliminarily functionalized at the polyfluoroaryl moiety through fluorine displacement with nucleophiles (methanol, methylamine, dimethylamine), allowing the obtainment of target indazoles substituted at the C(6) position.

MethylhydrazineIndazoleMethylamineOrganic ChemistrySettore CHIM/06 - Chimica OrganicaBiochemistryMedicinal chemistryChemical synthesischemistry.chemical_compoundchemistryNucleophileDrug DiscoveryStructural isomerMoietyOrganic chemistryDimethylamine124-Oxadiazole Indazole Rearrangements Fluorinated heterocycles
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Structural incorporation of nitrogen into zeolites, and alpos: ab initio molecular orbital calculations on stability and basicity

1998

Ab initio molecular orbital calculations (HF/6-31G*) are used to obtain thermodynamical information on the possibility to form NH-bridging or NH2-terminal groups in amorphous and crystalline materials containing Si–O–Si and Al–O–P structures, such as for instance, zeolites and aluminophosphates. We have employed dimeric model clusters Si–O–Si and Al–O–P which contain NH2-terminal groups or an oxygen atom substituted by a NH bridging unit. The Bronsted basicity and the softness–hardness of these structures have been determined using the proton affinity and the HOMO energy, respectively. The obtained results indicate that for both Si–O–Si and Al–O–P linkages and from a thermodynamic standpoin…

Process Chemistry and TechnologyAb initioMolecular sieveEndothermic processCatalysisCatalysisCrystallographychemistry.chemical_compoundchemistryComputational chemistryProton affinityMolecular orbitalPhysical and Theoretical ChemistryZeoliteDimethylamineJournal of Molecular Catalysis A: Chemical
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Role of the functional group in n-octydimethylsilanes in the synthesis of C8 reversed-phase silica packings for high-performance liquid chromatography

1986

Abstract C8 reversed-phase packings have been sysnthesised by reaction of a 25-nm pore-size high-performance liquid chromatographic silica (10 μm, as(BET) = 297 m2 g-1) with 2,4-lutidine as base and dichloromethane and N,N-dimethylflormamide as solvents, or without solvents and with the following silanes: n-octyldimenthylchlorosilane (C8-Cl), n-octyldimethylhydroxysilane (C8-OH), n-octyldimethylmethoxysilane (C8-OCH3), n-octyldimethylethoxysilane (C8-OC2H5), n-octyldimethyl(dimethylamino) silane [C8-N(CH3)2], n-octyldimethyl(trifluoroacetoxy)silane (C8- OCOCF3), and bis-(n-octyldimethylsiloxane) (C8-O-C8). C8-Cl, C8-OH and C8-OCH3 each form a reactive intermediate with 2,4-lutidine, favouri…

Reaction mechanismSilanesChromatographyOrganic ChemistryReactive intermediateGeneral MedicineBiochemistrySilaneAnalytical Chemistrychemistry.chemical_compoundchemistrySilanizationReactivity (chemistry)DimethylamineStoichiometryJournal of Chromatography A
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CCDC 679818: Experimental Crystal Structure Determination

2008

Related Article: C.Bonnot, J.-C.Chambron, E.Espinosa, R.Graff|2008|J.Org.Chem.|73|868|doi:10.1021/jo701984z

Space GroupCrystallography313-di-t-butyl-610-bis(p-tosyl)-678910111718-octahydro-5H-dibenzo[en][14812]dithiadiazacyclopentadecine-115-dicarbaldehyde N-methylformamide dimethylamine dichloromethane solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 907671: Experimental Crystal Structure Determination

2013

Related Article: Jochen Körber, Stefan Löffler, Dieter Schollmeyer, Udo Nubbemeyer|2013|Synthesis|45|2875|doi:10.1055/s-0033-1338519

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(2-((8-Chloro-5-oxidodibenzo[bf]thiepin-10-yl)oxy)ethyl)dimethylamine oxide dihydrateExperimental 3D Coordinates
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Synthesis and in vitro antileukemic activity of new 4-triazenopyrazole derivatives

2003

Several new 4-(3,3-dimethyltriazeno)-5-benzamidopyrazole derivatives were prepared by reacting 4-diazo-5-benzamidopyrazole derivatives with dimethylamine. The compounds were tested at 10 microM for their vitro antileukemic activity against K562 (Human chronic myelogenous leukemia) and Raji (human Burkitt limphoma ) cell lines. Dacarbazine and methotrexate were used for comparative purpose. The 3-methyl-4-(3,3-dimethyltriazeno)-5-(substituted benzamido)pyrazoles, bearing the pyrazole nucleus free at 1 position, resulted more active than the 1-(substituted phenyl)-3-methyl-4-(3,3-dimethyltriazeno)-5-benzamidopyrazoles. Dacarbazine at 10 microM showed no activity in the above tests. The observ…

StereochemistryDacarbazinePharmaceutical ScienceAntineoplastic AgentsPyrazoleSettore BIO/19 - Microbiologia GeneraleInhibitory Concentration 50Structure-Activity Relationshipchemistry.chemical_compoundCytochrome P-450 Enzyme SystemCell Line TumorLeukemia Myelogenous Chronic BCR-ABL PositiveDrug DiscoverymedicineHumansDimethylamine4-Triazenopyrazoles Antiproliferative activity In vitro antileukemic acitivityDemethylationTriazinesGeneral MedicineBurkitt LymphomaSettore CHIM/08 - Chimica FarmaceuticaIn vitroRaji cellchemistryMechanism of actionPyrazolesGrowth inhibitionmedicine.symptommedicine.drugIl Farmaco
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Mononuclear rearrangement of heterocycles in zwitterionic micelles of amine oxide surfactants.

2012

Abstract Rate constants for the mononuclear rearrangement (MRH) of Z -phenylhydrazones of some 5-substituted-3-benzoyl-1,2,4-oxadiazoles in water have been measured in the presence of zwitterionic micelles. The use of micellized N -tetradecyl- N , N -dimethylamineoxide (C 14 DMAO) as the reaction medium allowed to solubilize the otherwise water-insoluble oxadiazoles. Micellar rate effects were analyzed by using a simple pseudo-phase model and compared with those obtained in non-ionic micelles (Triton X-100). Evidence that both the rate of the rearrangement reaction and the binding of the substrates to the micelles are mainly governed by substrate hydrophobicity is obtained. The disagreement…

Steric effectsSpectrometry Mass Electrospray IonizationN-tetradecyl-NOctoxynolPhotochemistryMicelleMononuclear rearrangements of heterocycles (MHRs)Biomaterialschemistry.chemical_compoundSurface-Active AgentsColloid and Surface ChemistryReaction rate constantMicellar catalysiN-tetradecyl-NN-dimethylamineoxidePolymer chemistryRearrangement reactionzwitterionic micelleMicellesOxadiazolesHydrazonesSubstrate (chemistry)WaterSettore CHIM/06 - Chimica OrganicaSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmine oxideKineticschemistrySolubilitySolubilizationN-dimethylamineoxideThermodynamicsHydrophobic and Hydrophilic InteractionsMyristic AcidsDimethylaminesJournal of colloid and interface science
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Preparation of 2-amino-5-methyl-7H-1,3,4-thiadiazolo[3,2-α]pyrimidin-7-ones

2005

2-Amino substituted 7H-1,3,4-thiadiazolo[3,2-α]pyrimidin-7-ones 11a-e were prepared by the reaction of 2-bromo-5-amino-1,3,4-thiadiazole (1b) and diketene (8), subsequent cyclocondensation (9b 3b) and displacement of the bromo substituents by the reaction with primary or secondary amines (3b 11a-e). The hydrogen atom 6-H in the heterobicycle 3b is replaced by a Cl or Br atom in the transformation of 3b 14a,b. The 2-bromo-6-chloro compound 14a reacts chemoselectively in the 2-position with dimethylamine (14a 15). The structure elucidations are based on one- and two-dimensional NMR techniques including a heteronuclear NOE measurement.

Substitution reactionchemistry.chemical_compoundchemistryHeteronuclear moleculeStereochemistryOrganic ChemistryAtomGeneral MedicineHydrogen atomMedicinal chemistryDimethylamineDiketeneJournal of Heterocyclic Chemistry
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