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From this literature《Solvent Dependence of the Monomer-Dimer Equilibrium of Ketone-Substituted Triscatecholate Titanium(IV) Complexes》,we know some information about this compound(693-67-4)Computed Properties of C11H23Br, but this is not all information, there are many literatures related to this compound(693-67-4).

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Kwamen, A. Carel N.; Jenniches, Judith; Oppel, Iris M.; Albrecht, Markus researched the compound: 1-Bromoundecane( cas:693-67-4 ).Computed Properties of C11H23Br.They published the article 《Solvent Dependence of the Monomer-Dimer Equilibrium of Ketone-Substituted Triscatecholate Titanium(IV) Complexes》 about this compound( cas:693-67-4 ) in Chemistry – A European Journal. Keywords: titanium triscatecholate preparation monomer dimer equilibrium solvent effect; helicates; intermolecular interactions; self assembly; solvent effect; thermodynamics. We’ll tell you more about this compound (cas:693-67-4).

Hierarchical helicates based on ketone-substituted titanium(IV)triscatecholates show different monomer-dimer behavior depending on different solvents. The dimerization constants of a whole series of differently alkyl-substituted complexes is analyzed to show that the solvent has a very strong influence on the dimerization. Hereby, effects like solvophobicity/philicity, sterics, electronics of the substituents and weak side-chain-side-chain interactions seem to act in concert.

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From this literature《The effects of single administration of an antitumor platinum compound on ornithine decarboxylase activity in certain tissues of mice bearing L1210 leukemia》,we know some information about this compound(15227-42-6)Category: tetrahydroisoquinoline, but this is not all information, there are many literatures related to this compound(15227-42-6).

Category: tetrahydroisoquinoline. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: cis-Dichlorobis(pyridine)platinum(II), is researched, Molecular C10H10Cl2N2Pt, CAS is 15227-42-6, about The effects of single administration of an antitumor platinum compound on ornithine decarboxylase activity in certain tissues of mice bearing L1210 leukemia. Author is Morris, Carl R.; Atkins, Loretta M.; Gale, Glen R..

A single dose of cis-dichloro(dipyridine)platinum(II) [15227-42-6], when given to mice bearing 1-day-old L1210 leukemia, suppressed the increase of spleen and liver ornithine decarboxylase (ODC) [9024-60-6] activity which occurs concomitantly with development of the leukemia. The inhibition of ODC, the rate-limiting enzyme in polyamine synthesis, appeared to correlate with the prolonged chemotherapeutic efficacy of a single dose of the platinum complex. These observations suggest an addnl. mechanism by which platinum complexes express their antitumor actions and, in addition, support the view that polyamine synthesis and excretion patterns can be used as predictors of chemotherapeutic response.

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From this literature《Oxidation of platinum(II) complexes by antimony pentachloride derivatives》,we know some information about this compound(15227-42-6)Application In Synthesis of cis-Dichlorobis(pyridine)platinum(II), but this is not all information, there are many literatures related to this compound(15227-42-6).

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Oxidation of platinum(II) complexes by antimony pentachloride derivatives, published in 1989, which mentions a compound: 15227-42-6, mainly applied to platinum 2 complex oxidation; antimony chloro derivative oxidation platinum 2; glycine platinum 2 oxidation; pyridine platinum 2 oxidation, Application In Synthesis of cis-Dichlorobis(pyridine)platinum(II).

[Ph3PCH2Ph]2[PtXCl3] (X = Cl, NO2) are oxidized by Sb(BzCl)Cl5 (I) or Et3NCH2Ph[SbCl6] (II) in MeNO2, MeCN or DMF to give (Ph3PCH2Ph)2[PtXCl5]. SbCl5 oxidizes cis- and trans-Pt(py)2Cl2 to give cis- and trans-[Pt(py)2Cl4], resp. I oxidizes trans-[Pt(NH2CH2CO2H)2Cl2] to give trans-[Pt(NH2CH2CO2H)2Cl4] which on reaction with PCl5 in MeCN gives trans-[Pt(NH2CH2COCl)2Cl4]. [Pt(py)4]Cl2 reacted with I to give trans-[Pt(py)2Cl4]. cis- And trans-[PtL2Cl2] (L = PPh3, SMe2) are not oxidized by I or II.

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From this literature《Separation of square planar complexes by thin layer chromatography》,we know some information about this compound(15227-42-6)Name: cis-Dichlorobis(pyridine)platinum(II), but this is not all information, there are many literatures related to this compound(15227-42-6).

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Separation of square planar complexes by thin layer chromatography, published in 1966, which mentions a compound: 15227-42-6, mainly applied to PYRIDINE COMPLEX CHROMATOG; THIN LAYER CHROMATOG; CHROMATOG SEPN SQUARE PLANAR COMPLEX; PLATINUM COMPLEX CHROMATOG; PALLADIUM COMPLEX CHROMATOG; SEPN SQUARE PLANAR COMPLEX, Name: cis-Dichlorobis(pyridine)platinum(II).

Uncharged sq. planar Pt and Pd complexes were separated by using plates with a 100 μ coating of silica gel bound by poly(vinyl alc.) and activated for 30 min. at 115°. The solvent was HCCl3 containing 3 drops Me2SO per 100 ml. Typical Rf values are given. Separation of cis- and trans-Ptpy2X2 (X = Cl, Br) was particularly successful, while cis- and trans-Pt(NH3)2Cl2 could not be separated The mechanism of separation appears to be via surface adsorption. Layer thickness, activation conditions, and solvent travel time are therefore very critical

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Product Details of 882562-40-5. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 3-(2,5-Dichloropyrimidin-4-yl)-1-(phenylsulfonyl)-1H-indole, is researched, Molecular C18H11Cl2N3O2S, CAS is 882562-40-5, about Structure- and Reactivity-Based Development of Covalent Inhibitors of the Activating and Gatekeeper Mutant Forms of the Epidermal Growth Factor Receptor (EGFR). Author is Ward, Richard A.; Anderton, Mark J.; Ashton, Susan; Bethel, Paul A.; Box, Matthew; Butterworth, Sam; Colclough, Nicola; Chorley, Christopher G.; Chuaqui, Claudio; Cross, Darren A. E.; Dakin, Les A.; Debreczeni, Judit E.; Eberlein, Cath; Finlay, M. Raymond V.; Hill, George B.; Grist, Matthew; Klinowska, Teresa C. M.; Lane, Clare; Martin, Scott; Orme, Jonathon P.; Smith, Peter; Wang, Fengjiang; Waring, Michael J..

A novel series of small-mol. inhibitors has been developed to target the double mutant form of the epidermal growth factor receptor (EGFR) tyrosine kinase, which is resistant to treatment with gefitinib and erlotinib. Our reported compounds also show selectivity over wild-type EGFR. Guided by mol. modeling, this series was evolved to target a cysteine residue in the ATP binding site via covalent bond formation and demonstrates high levels of activity in cellular models of the double mutant form of EGFR. In addition, these compounds show significant activity against the activating mutations, which gefitinib and erlotinib target and inhibition of which gives rise to their observed clin. efficacy. A glutathione (GSH)-based assay was used to measure thiol reactivity toward the electrophilic functionality of the inhibitor series, enabling both the identification of a suitable reactivity window for their potency and the development of a reactivity quant. structure-property relationship (QSPR) to support design.

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Archives for Chemistry Experiments of 1452-77-3

From this literature《Green ultrasound assisted magnetic nanofluid-based liquid phase microextraction coupled with gas chromatography-mass spectrometry for determination of permethrin, deltamethrin, and cypermethrin residues》,we know some information about this compound(1452-77-3)Name: Picolinamide, but this is not all information, there are many literatures related to this compound(1452-77-3).

Name: Picolinamide. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: Picolinamide, is researched, Molecular C6H6N2O, CAS is 1452-77-3, about Green ultrasound assisted magnetic nanofluid-based liquid phase microextraction coupled with gas chromatography-mass spectrometry for determination of permethrin, deltamethrin, and cypermethrin residues. Author is Shirani, Mahboube; Akbari-adergani, Behrouz; Jazi, Masoud Boroumand; Akbari, Ali.

Ultrasound-assisted magnetic nanofluid-based liquid-phase microextraction was coupled to GC-MS in a method for simultaneous determination of the pyrethroid insecticides permethrin, deltamethrin, and cypermethrin. A highly efficient extraction solvent called “”magnetic nanofluid (MNF)”” is introduced for preconcentration of pyrethroids. The MNF consists of magnetic multiwalled carbon nanotubes (MMWCNTs) and deep eutectic solvent. Following microextraction, the MNF was detached by an external magnet from the medium without the need for centrifugation. 2-Pyridinecarboxamide, choline chloride, and anhydrous ferric chloride were used for the synthesis of the deep eutectic solvent. The effects of pH value, volume of MNF, sonication time, sample volume, and ionic strength, type and amount of back extraction solvent were investigated. Under optimum conditions of MNF volume of 50μL, time of 5 min, 100μL acetone as back extraction solvent, NaCl concentration of 1 mol.L-1 and sample volume of 30 mL, the detection limits are 2.8, 2.7 and 2.0 ng.mL-1 for permethrin, deltamethrin and cypermethrin, resp. The linear response ranges are between 0.01 and 250 ng.mL-1, and relative standard deviations (for n = 7) are 3.5, 3.2 and 2.8%. The method was successfully applied to the determination of trace levels of permethrin, deltamethrin and cypermethrin in (spiked) milk samples.

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Our Top Choice Compound: 15227-42-6

From this literature《The investigation of platinum(II) complexes with adenine, adenosine and 2-aminopyrimidines》,we know some information about this compound(15227-42-6)Application of 15227-42-6, but this is not all information, there are many literatures related to this compound(15227-42-6).

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: cis-Dichlorobis(pyridine)platinum(II)( cas:15227-42-6 ) is researched.Application of 15227-42-6.Stetsenko, A. I.; Dmitrieva, E. S.; Yakovlev, K. I. published the article 《The investigation of platinum(II) complexes with adenine, adenosine and 2-aminopyrimidines》 about this compound( cas:15227-42-6 ) in Journal of Clinical Hematology and Oncology. Keywords: platinum adenine adenosine aminopyrimidine; adenine platinum complex; adenosine platinum complex; aminopyrimidine platinum complex; pyrimidine amino platinum complex; ammine platinum complex; pyridine platinum complex; ethylenediamine platinum complex. Let’s learn more about this compound (cas:15227-42-6).

[Pt2(NH3)4Cl2L]Cl2 (L = adenine, adenosine) were prepared by the addition of ligand to cis-[Pt(NH3)2Cl2] solution [Pt(NH3)2L](NO3)2 were obtained by adding L to cis-[Pt(NH3)2(H2O)2](NO3)2 solution 2-Aminopyrimidine (L1) and 2-amino-4-phenylpyrimidine (L2) reacted with aqueous K2[PtCl4] to yield trans-[PtL12Cl2] and trans-[PtL22Cl2], resp. The cis-[PtA2L12]Cl2 (A = NH3, pyridine, 0.5 ethylenediamine) were obtained by the substitution reaction of cis-[PtA2Cl2] with 2-aminopyrimidine. The cis-[PtA2(H2O)2](NO3)2 reacted with 2-aminopyrimidine to afford cis-[PtA2L12](NO3)2 and cis-[PtA2L1](NO3)2 (A = NH3, 0.5 ethylenediamine), depending on the stoichiometric ratios of the reactants.

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The Absolute Best Science Experiment for 15227-42-6

From this literature《Solid-phase thermal transformations of platinum(IV) aminate complexes》,we know some information about this compound(15227-42-6)SDS of cas: 15227-42-6, but this is not all information, there are many literatures related to this compound(15227-42-6).

SDS of cas: 15227-42-6. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: cis-Dichlorobis(pyridine)platinum(II), is researched, Molecular C10H10Cl2N2Pt, CAS is 15227-42-6, about Solid-phase thermal transformations of platinum(IV) aminate complexes. Author is Kukushkin, Yu. N.; Sedova, G. N.; Belyaev, A. N.; Konovalov, L. V..

The thermal behavior of onium chloroplatinates of the type (AH)2[PtCl6] (A = NH3, MeNH2, 0.5 en, piperidine, py, γ-picoline, NH2Ph, p-toluidine, quinoline, 0.5 2,2′-bipyridine) was studied by derivatog. and IR spectral anal. The heating of solid (AH)2[PtCl6] led to the formation of trans-PtL2Cl4 (L = py, γ-picoline) and cis-PtQ2Cl4 (Q = p-toluidine) and subsequently to the formation of cis-PtA2Cl2. When (AH)2[PtCl6] (A = piperidine) was heated (AH)2[PtCl4] was formed. These results were compared with those for the corresponding palladates.

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In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called α-Hydroxy-Tetrazoles as Latent Ethynyl Moieties: A Mechanistic Investigation, published in 2019, which mentions a compound: 57399-11-8, Name is 4-Chloro-4′-ethynyl-1,1′-biphenyl, Molecular C14H9Cl, Application of 57399-11-8.

This article focuses on the dehydration of α-hydroxy-tetrazoles, leading to tetraazafulvenes and then to vinylic carbenes that rearrange into ethynyl moieties through the Fritsch-Buttenberg-Wiechell rearrangement. Each step of this sequence was scrutinized, either by examination of the substrate and/or dehydrating agent scope, or through AM1 calculations, to understand the limiting step of this process. This underrated transformation appears to be a viable alternative to existing methods used for transforming aldehydes into alkynes.

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From this literature《Understanding the extraction behaviour of UO2+2 and Th4+ using novel picolinamide/N-oxo picolinamide in ionic liquid: A comparative evaluation with molecular diluent》,we know some information about this compound(1452-77-3)Recommanded Product: 1452-77-3, but this is not all information, there are many literatures related to this compound(1452-77-3).

Recommanded Product: 1452-77-3. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: Picolinamide, is researched, Molecular C6H6N2O, CAS is 1452-77-3, about Understanding the extraction behaviour of UO2+2 and Th4+ using novel picolinamide/N-oxo picolinamide in ionic liquid: A comparative evaluation with molecular diluent. Author is Das, Debasish; Hashmi, Sabiha; Sengupta, Arijit; Kannan, S.; Kaushik, C. P..

The manuscript deals with efficient separation of hexavalent UO2+2 and tetravalent Th4+ from aqueous acidic waste solution in green way using ionic liquid with novel picolinamide (L I) and N-oxo picolinamide (L II) based ligands. A comparative evaluation was carried out to understand the extraction mechanism, kinetics, thermodn., speciation, radiolytic stability and stripping behavior of UO2+2 and Th4+ in ionic liquid vis-a-vis mol. diluent. The investigation demonstrates the predominance of cation exchange mechanism in ionic liquid and solvation mechanism in n-dodecane based systems. The slower extraction kinetics in ionic liquid was attributed to the viscosity effect. The extractive mass transfer processes were found to be spontaneous, endothermic and entropically driven in nature. The picolinamide and N-oxo picolinamide ligands were found to form inner-sphere complexes in ionic liquid as well as n-dodecane. The CO2-3 was more effective aqueous phase complexing agent to back extract UO2+2, while C2O2-4 exhibited the same for Th4+.

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