Extended knowledge of 17190-29-3

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Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 17190-29-3, is researched, Molecular C9H9NO, about Unexpected Stereorecognition in Nitrilase-Catalyzed Hydrolysis of β-Hydroxy Nitriles, the main research direction is nitrile hydroxy preparation enantioselective enzymic hydrolysis nitrilase; carboxylic acid hydroxy aryl asym synthesis.Recommanded Product: 17190-29-3.

Biocatalytic enantioselective hydrolysis of β-hydroxy nitriles RCH(OH)CH2CN (R = Ph, 4-FC6H4, 2-MeOC6H4, 2,4-Cl2C6H3, etc.) to the corresponding (S)-enriched β-hydroxy carboxylic acids RCH(OH)CH2COOH has been achieved for the first time by an isolated nitrilase bll6402 from Bradyrhizobium japonicum USDA110. This offers a new “”green”” approach to optically pure β-hydroxy nitriles and β-hydroxy carboxylic acids. The observed remote stereorecognition is surprising because this nitrilase shows no enantioselectivity for the hydrolysis of α-hydroxy nitriles such as mandelonitrile.

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Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Machine Learning in Chemistry about 25956-17-6

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The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate( cas:25956-17-6 ) is researched.Related Products of 25956-17-6.Khan, Menhad; Khan, Adnan; Khan, Hammad; Ali, Nisar; Sartaj, Seema; Malik, Sumeet; Ali, Nauman; Khan, Hamayun; Shah, Sumaira; Bilal, Muhammad published the article 《Development and characterization of regenerable chitosan-coated nickel selenide nano-photocatalytic system for decontamination of toxic azo dyes》 about this compound( cas:25956-17-6 ) in International Journal of Biological Macromolecules. Keywords: chitosan nickel selenide toxic azo dye photocatalytic decontamination; Chitosan; Degradation; Nickel selenide; Organic pollutants; Photocatalyst; Reusability. Let’s learn more about this compound (cas:25956-17-6).

In this investigation, chitosan-coated nickel selenide nano-photocatalyst (CS-NiSe) was successfully prepared through the chem. reduction method. FTIR spectroscopy confirmed the synthesis of CS-NiSe nano-photocatalyst. Further, XRD anal. exhibited a monoclinic crystalline phase of photocatalyst with a crystallite size of 32 nm based on Scherer’s equation. The SEM micrographs showed that the photocatalyst has an average particle size of 60 nm. The bandgap of CS-NiSe was (2.85 eV) in the visible region of the spectrum. Due to this reason, the CS-NiSe was applied under solar light illumination for the photocatalytic activity of Erythrosine and Allura red dyes. The CS-NiSe presented the highest degradation efficiency of 99.53% for Erythrosine dye in optimized exptl. conditions of 100 min at 30°C, 30 ppm concentration, pH 5.0, and 0.14 g catalyst dose. For Allura red dye, a high degradation of 96.12% was attained in 120 min at pH 4.0, 100 ppm initial dye concentration, 35°C temperature, and 0.1 g catalyst dose. The CS-NiSe showed excellent degradation efficiency and reduced to (95% for Erythrosine and 91% for Allura red dye) after five consecutive batches. Moreover, the statistical and neural network modeling anal. showed the significant influence of all studied variables on dyes degradation performance. The results demonstrated that CS-NiSe exhibited excellent photocatalytic performances for Erythrosine and Allura red dyes and could be a better photocatalyst for removing these dyes from industrial effluents.

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Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Continuously updated synthesis method about 17190-29-3

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Category: pyrazoles-derivatives. 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. Compound: 3-Hydroxy-3-phenylpropanenitrile, is researched, Molecular C9H9NO, CAS is 17190-29-3, about Addition of α-Halo-substituted Carbonitriles to Aldehydes and Ketones in the Presence of Iron Pentacarbonyl.

Halo-substituted carbonitriles in the presence of iron pentacarbonyl react with aldehydes and ketones by Reformatsky reaction type. In contract to halo-substituted esters the nitriles are considerably more reactive toward ketones than aldehydes. At the same time the structure and yield of products obtained from both nitriles and esters are strongly and similarly affected by the character of the para-substituents in the benzaldehyde. Thus, Fe(CO)5-mediated reaction of ICH2CN with 2-hexanone in C6H6 gave 70% 3-hydroxy-3-methylenanthonitrile.

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Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

The effect of the change of synthetic route on the product 17190-29-3

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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 Preparation of β-hydroxyesters from isoxazolines. A selective Ni0bpy-catalyzed electrochemical method, published in 2003-11-03, which mentions a compound: 17190-29-3, Name is 3-Hydroxy-3-phenylpropanenitrile, Molecular C9H9NO, Quality Control of 3-Hydroxy-3-phenylpropanenitrile.

An electrocatalytic method for the reductive N-O cleavage of isoxazolines I [R1 = Ph; R2 = H; R3 = OMe, Br; R1R2 = (CH2)4; R3 = OMe], is described. Ni0bpy, generated in situ, was used to promote selective ring opening of I. DMF and NaI were used as solvent and supporting electrolyte resp., and β-hydroxyesters were obtained in high yields, after acid hydrolysis. β-Hydroxynitriles were also identified as side products.

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Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Continuously updated synthesis method about 17190-29-3

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Category: pyrazoles-derivatives. 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: 3-Hydroxy-3-phenylpropanenitrile, is researched, Molecular C9H9NO, CAS is 17190-29-3, about Reformatskii type additions of haloacetonitriles to aldehydes mediated by metallic nickel. Author is Inaba, Shinichi; Rieke, Reuben D..

β-Hydroxy nitriles HOCHRCH2CN [R = (un)substituted Ph, styryl, alkyl, alkenyl] were prepared by Reformatskii type addition of haloacetonitriles to aldehydes RCHO in the presence of metallic Ni (generated in situ).

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Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Chemical Research in 22600-77-7

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Recommanded Product: 22600-77-7. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: (1H-Imidazol-2-yl)methanamine dihydrochloride, is researched, Molecular C4H9Cl2N3, CAS is 22600-77-7, about Development of Selective Clk1 and -4 Inhibitors for Cellular Depletion of Cancer-Relevant Proteins. Author is ElHady, Ahmed K.; Abdel-Halim, Mohammad; Abadi, Ashraf H.; Engel, Matthias.

In cancer cells, kinases of the Clk family control the supply of full-length, functional mRNAs coding for a variety of proteins essential to cell growth and survival. Thus, inhibition of Clks might become a novel anticancer strategy, leading to a selective depletion of cancer-relevant proteins after turnover. On the basis of a Weinreb amide hit compound, the authors designed and synthesized a diverse set of methoxybenzothiophene-2-carboxamides, of which the N-benzylated derivative showed enhanced Clk1 inhibitory activity. Introduction of a m-fluorine in the benzyl moiety eventually led to the discovery of compound 21b (5-methoxybenzo[b]thiophene-2-carboxylic acid (3-fluorobenzyl)methylamide), a potent inhibitor of Clk1 and -4 (IC50 = 7 and 2.3 nM, resp.), exhibiting an unprecedented selectivity over Dyrk1A. Compound 21b triggered the depletion of EGFR, HDAC1, and p70S6 kinase from the cancer cells, with potencies in line with the measured GIC50 values. In contrast, the cellular effects of congener 21a (5-methoxybenzo[b]thiophene-2-carboxylic acid 3-fluorobenzylamide), which inhibited Clk1 only weakly, were substantially lower.

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Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

New explortion of 814-94-8

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COA of Formula: C2O4Sn. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: Tin(II) oxalate, is researched, Molecular C2O4Sn, CAS is 814-94-8, about A new lithium diffusion model in layered oxides based on asymmetric but reversible transition metal migration. Author is Ku, Kyojin; Kim, Byunghoon; Jung, Sung-Kyun; Gong, Yue; Eum, Donggun; Yoon, Gabin; Park, Kyu-Young; Hong, Jihyun; Cho, Sung-Pyo; Kim, Do-Hoon; Kim, Hyungsub; Jeong, Eunsuk; Gu, Lin; Kang, Kisuk.

Lithium-rich layered oxides (LLOs) are considered promising cathode materials for lithium-ion batteries because of their high reversible capacity, which is attributed to the exploitation of the novel anionic redox in addition to the conventional cationic redox process. Transition metal (TM) migration, which is known to be the main cause of the voltage decay in LLOs, is now understood to also be the critical factor triggering anionic redox, although this origin is still under debate. A better understanding of the specific TM migration behavior and its effect during charge/discharge would thus enable further development of this class of materials. Herein, we demonstrate that the unique TM migration during charge/discharge significantly alters the lithium diffusion mechanism/kinetics of LLO cathodes. We present clear evidence of the much more sluggish lithium diffusion occurring during discharge (lithiation) than during charge (de-lithiation), which contrasts with the traditional lithium diffusion model based on simple topotactic lithium intercalation/deintercalation in the layered framework. The reversible but asym. TM migration in the structure, which originates from the non-equivalent local environments around the TM during the charge and discharge processes, is shown to affect the lithium mobility. This correlation between TM migration and lithium mobility led us to propose a new lithium diffusion model for layered structures and suggests the importance of considering TM migration in designing new LLO cathode materials.

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Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Extracurricular laboratory: Synthetic route of 17190-29-3

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Application of 17190-29-3. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 3-Hydroxy-3-phenylpropanenitrile, is researched, Molecular C9H9NO, CAS is 17190-29-3, about Synthetic application of cyanoaminosilanes as azomethine ylide equivalents. Author is Padwa, Albert; Chen, Yon Yih; Dent, William; Nimmesgern, Hildegard.

A series of α-cyanoaminosilanes acted as azomethine ylide equivalent Treatment of these compounds with AgF in the presence of electron-deficient alkynes and olefins gives substituted pyrroles and pyrrolidines in high yield. Me3SiCH2N(CH2Ph)CH2CN (I) undergoes stereospecific cycloaddition with di-Me fumarate and maleate. The stereospecificity of the reaction is consistent with a concerted cycloaddition reaction. The cycloaddition behavior of an unsym. substituted α-cyanosilylamine with MeO2CCCH was also examined and found to react with high overall regioselectivity. The synthetic utility of cyanoaminosilanes as azomethine ylide equivalent was demonstrated by the preparation of a Reniera isoindole alkaloid (II). The key step in the synthesis involved the reaction of 2-methyl-3-methoxyquinone with I in the presence of AgF to give 2,5-dimethyl-6-methoxyisoindole-4,7-dione in good yield.

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Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

A new application about 25956-17-6

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Staples, Jack W.; Stine, Jessica M.; Maki-Lohiluoma, Eero; Steed, Emily; George, Kathleen M.; Thompson, Charles M.; Woodahl, Erica L. published the article 《Food dyes as P-glycoprotein modulators》. Keywords: allurared carmoisine ponceau4R sunset quinolone yellow tartrazine AtPase Pglycoprotein; Drug transporter; Food dye; P-glycoprotein.They researched the compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate( cas:25956-17-6 ).SDS of cas: 25956-17-6. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:25956-17-6) here.

The drug transporter P-glycoprotein (P-gp) is often investigated in drug-interaction studies because the activity is modulated by a wide variety of xenobiotics including drugs, herbal products, and food components. In this study, we tested six common arylsulfonate food dyes-allura red, carmoisine, ponceau 4R, quinolone yellow, sunset yellow, and tartrazine-as activators and inhibitors of P-gp activity in vitro. The dyes were studied as P-gp activators by measuring ATPase activity in P-gp-expressing membranes. Compared to verapamil, a known activator of P-gp, the six food dyes showed no stimulatory activity. The potential for these six food dyes to act as P-gp inhibitors was tested in an intracellular efflux assay with P-gp-expressing cells. Compared to GF120918, a known P-gp inhibitor, there was no inhibitory activity for these six food dyes. The six food dyes tested do not interact with P-gp in vitro and, therefore, are unlikely cause clin. drug-food dye interactions. Further investigation is necessary to determine whether these food dyes could interact with other drug transporters.

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Pyrazole – Wikipedia,
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Awesome Chemistry Experiments For 52287-51-1

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Recommanded Product: 52287-51-1. 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: 6-Bromo-2,3-dihydrobenzo[b][1,4]dioxine, is researched, Molecular C8H7BrO2, CAS is 52287-51-1, about 6-(4-Benzylpiperazin-1-yl)benzodioxanes as selective ligands at cloned primate dopamine D4 receptors. Author is Hodgetts, Kevin J.; Kieltyka, Andrzej; Brodbeck, Robbin; Tran, Jennifer N.; Wasley, Jan W. F.; Thurkauf, Andrew.

A series of novel 6-(4-benzylpiperazin-1-yl)benzodioxanes were prepared and screened at selected dopamine receptor subtypes. 6-(4-[4-Chlorobenzyl]piperazin-1-yl)benzodioxane had high affinity and selectivity for the D4 dopamine receptor subtype and was identified as a D4 antagonist via its attenuation of dopamine-induced GTPγ35S binding at the D4 receptor.

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Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics