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Related Products of 497-25-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.497-25-6, Name is Oxazolidin-2-one, molecular formula is C3H5NO2. In a Article，once mentioned of 497-25-6

We prepared gold nanoparticles encapsulated in poly(amidoamine) (PAMAM) dendrimers as templating agents. The resulting gold nanoparticles were used as catalysts for the carboxylative cyclization of propargylic amines with carbon dioxide to afford the corresponding 1,3-oxazolidin-2-ones in yields of up to 99%.

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Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H802NO – PubChem

Synthetic Route of 497-25-6, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Article, and a compound is mentioned, 497-25-6, Oxazolidin-2-one, introducing its new discovery.

The zwitterionic intermediate generated from the reaction of triphenylphosphine with electron deficient acetylenic compounds was trapped by various NH acids. The synthesis resulted in a new class of highly functionalized heterocyclic compounds. Some of the reactions produced E and Z isomers. And the stability and transformation of them were studied by dynamic 1H NMR and density functional theory (DFT) calculations.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 497-25-6. In my other articles, you can also check out more blogs about 497-25-6

Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H969NO – PubChem

497-25-6, Name is Oxazolidin-2-one, belongs to oxazolidine compound, is a common compound. SDS of cas: 497-25-6In an article, once mentioned the new application about 497-25-6.

This paper describes a novel approach to CO2 hydrogenation, in which CO2 capture with aminoethanols at low pressure is coupled with hydrogenation of the captured product, oxazolidinone, directly to MeOH. In particular, (2-methylamino)ethanol or valinol captures CO2 at 1-3 bar in the presence of catalytic Cs2CO3 to give the corresponding oxazolidinones in up to 65-70 and 90-95% yields, respectively. Efficient hydrogenation of oxazolidinones was achieved using PNN pincer Ru catalysts to give the corresponding aminoethanol (up to 95-100% yield) and MeOH (up to 78-92% yield). We also have shown that both CO2 capture and oxazolidinone hydrogenation can be performed in the same reaction mixture using a simple protocol that avoids intermediate isolation or purification steps. For example, CO2 can be captured by valinol at 1 bar with Cs2CO3 catalyst followed by 4-isopropyl-2-oxazolidinone hydrogenation in the presence of a bipy-based pincer Ru catalyst to produce MeOH in 50% yield after two steps.

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Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H690NO – PubChem

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 497-25-6, name is Oxazolidin-2-one, introducing its new discovery. Product Details of 497-25-6

Poly(urethane-oxazolidone) were synthesized by reacting isocyanate-terminated oxazolidone with hydroxy-telechelic poly(tetramethylene oxide) (PTMO). The molar ratios of the reactants were varied to get polymers of varying oxazolidone and urethane compositons. The polymers were characterized by DSC, FTIR, XRD, dynamic mechanical thermal analysis and chemical analyses. An increase in the concentration of urethane and oxazolidone groups caused a decrease in tensile strength and elongation of the poly(urethane-oxazolidone). The polymers possessed crystallites of PTMO whose melting transition temperature decreased on enhancing the oxazolidone concentration. The polymers exhibited thermo-responsive shape memory properties, which was confirmed and quantified by cyclic tensile tests. The influence of oxazolidone modification and the consequent soft/hard segment variation on the thermal, mechanical, dynamic-mechanical and shape recovery properties of the resultant polymers was investigated. The oxazolidone moities conferred enhanced shape recovery and shape fixity to the polyurethane.

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Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H810NO – PubChem

Application of 497-25-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.497-25-6, Name is Oxazolidin-2-one, molecular formula is C3H5NO2. In a Patent，once mentioned of 497-25-6

The present invention relates to compounds of formula (I): in which Y, Y, R, R2, R3 and R4 are defined in the Summary of the Invention; capable of inhibiting the activity of BCR-ABL1 and mutants thereof. The invention further provides a process for the preparation of compounds of the invention, pharmaceutical preparations comprising such compounds and methods of using such compounds in the treatment of cancers

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Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H98NO – PubChem

Reference of 497-25-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.497-25-6, Name is Oxazolidin-2-one, molecular formula is C3H5NO2. In a Patent，once mentioned of 497-25-6

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I): and salts thereof. The compounds of the invention are inhibitors of kinase activity, in particular Itk activity

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Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H9NO – PubChem

Application of 497-25-6, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 497-25-6, molcular formula is C3H5NO2, introducing its new discovery.

The effect of tethering a thioether to a rhodium(II) paddlewheel complex are evaluated in Si?H insertion reactions. This study provides further evidence for the benefits of incorporating thioethers into the rhodium paddlewheel motif. When using a tethered complex, the in situ carbenoid formation and subsequent Si?H insertion are not impeded, yields are improved by up to 12 % at elevated temperatures, and selectivity for diazo compounds is greater when compared to non-tethered catalysts. Computational modelling of the complexes is also presented in order to rationalize the results.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 497-25-6 is helpful to your research. Application of 497-25-6

Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H976NO – PubChem

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Recommanded Product: Oxazolidin-2-one, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 497-25-6, name is Oxazolidin-2-one. In an article，Which mentioned a new discovery about 497-25-6

Amine-based CO2 capture (ACC) has become one cost-effective method for reducing carbon emissions in order to mitigate climate changes. The amine-rich wastewater (ARWW) generated from ACC may contain a series of degradation products of amine-based solvents (ABSs). These products are harmful for ecological environment and human health. Effective and reliable ARWW treatment methods are highly required for mitigating the harmfulness. However, there is a lack of a comprehensive review of the existing limited methods that can guide ARWW-related technological advancements and treatment practices. To fill this gap, the review is achieved in this study. All available technologies for treating the ARWW from washwater, condenser, and reclaimer units in ACC are examined based on clarification of degradation mechanisms and ARWW compounds. A series of significant findings and recommendations are revealed through this review. For instance, ARWW treatment methods should be selected according to degradation conditions and pollution concentrations. UV light can be only used for treating wastewater from washwater and condenser units in ACC. Biological activated carbon is feasible for removing nitrosamines from washwater and condenser units. Sequence batch reactors, microbial fuel cells, and the other techniques for removing amines and similar degradation products are applicable for treating ARWW. This review provides scientific support for the selection and improvement of ARWW treatment techniques, the mitigation of ACC’s consequences in environment, health and other aspects, and the extensive development and applications of ACC systems.

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Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H498NO – PubChem

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Product Details of 497-25-6, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 497-25-6, Name is Oxazolidin-2-one, molecular formula is C3H5NO2

3-[(4-Substituted) (2-oxo-1,3-oxazolidin-3-yl)-phosphoryl]-1,3-oxazolidin- 2-ones (4a-j) were synthesized through a two-step process. Bis-(2-oxo-1,3- oxazolidin-3-yl)-phosphonic chloride (2) prepared by the reaction of two moles of oxazolidin-2-one (1) with phosphorus oxychloride in dry tetrahydrofuran in the presence of triethylamine and treatment with various heterocyclic aromatic and aliphatic amines under the same experimental conditions afforded the title compounds (4a-j). They were characterized by elemental analysis, IR, NMR ( 1H, 13C and 31P) and mass spectroscopy. Their antimicrobial activities were also evaluated.

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Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H928NO – PubChem

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 497-25-6, name is Oxazolidin-2-one, introducing its new discovery. Recommanded Product: 497-25-6

The conjugate addition nitro-Mannich reactions of ethyl-beta-nitroacrylate (1) and beta-nitrostyrene (2) with electron rich aromatic nucleophiles, stabilized carbanions, alcohols, amines, thiols, and diphenyl phosphine oxide were investigated. The one pot conjugate addition nitro-Mannich reaction was unsuccessful except for the addition of alkoxides to 2 in alcohol as solvent. Isolation of the conjugate addition products followed by deprotonation with nBuLi and treatment with a simple imine in the presence of TFA led to beta-nitroamine derived products. Products derived from 1 spontaneously cyclised in only a few examples and on the whole led to inherently unstable products. Products derived from 2 were isolated as their trifluoroacetamides, gave good yields of single diastereoisomers for aromatic and alkoxide nucleophiles and the structures were verified by single crystal X-ray crystallography. Products derived from amine nucleophiles were isolated in low yields while sulfur nucleophiles gave poor diastereoselectivities.

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Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H299NO – PubChem