Category: 117977-21-6

As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 117977-21-6, name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, molecular formula is C18H21N3O2S, The compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below. COA of Formula: C18H21N3O2S

50 g of 2-[4-(3-methoxy propoxy-3-methylpyridine-2-yl) methyl thio]- lH-benzimidazole was taken in 100 ml acetonitrile. To this mixture 185.2 g (0.95mol) sodium hypochlorite was added drop wise between 0-50C in a nitrogen atmosphere and the obtained mixture was stirred at 0-50C for 30 minutes. After completion of reaction, the pH of reaction mixture was adjusted to 9.0 by using 5 % acetic acid. The mixture was extracted with methylene dichloride, and the extract was dried over sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and dried under vacuum. The obtained residue was dissolved in 20 ml of methylene dichloride followed by t-butyl methyl ether to get the clear solution. Stir the mass for one hour at room temperature to get the precipitate. Filtered the precipitated product and washed with 100 ml of t-butyl methyl ether. Dry the product at 600C under vacuum to obtain title compound 41 g (78.25%) as off white solid

With the rapid development of chemical substances, we look forward to future research findings about 117977-21-6.

Reference:
Patent; IPCA LABORATORIES LIMITED; WO2009/116072; (2009); A2;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, SMILES is COCCCOC1=C(C(=NC=C1)CSC2=NC3=C([NH]2)C=CC=C3)C, belongs to pyridine-derivatives compound. In a document, author is Bhoi, Manoj N., introduce the new discover, Name: 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole.

Novel benzothiazole containing 4H-pyrimido[2,1-b]benzothiazoles derivatives: One pot, solvent-free microwave assisted synthesis and their biological evaluation

Synthesis of new and desired compounds has an everlasting demand. The present work emphasizes on the one pot, three component microwave assisted synthesis of novel ethyl 2-methyl-4-(pyridin-2-yl)-4H-benzo[4,5]thiazolo[3,2-a]pyrimidine-3-carboxylate derivatives by the reaction of 2-aminobenzothiazole derivatives with Pyridine 2-aldehyde and Ethyl acetoacetate in the presence of PdCl2 as an expeditious catalyst under solvent-free condition. The salient features of this approach are operational simplicity, convergence, short reaction time, high atom economy, easy workup, mild reaction conditions and environmentally benign conditions. All the newly synthesized diverse poly-functionalized tri-heterocyclic benzothiazole derivatives have been characterized by elemental analysis and various spectroscopic methods such as FT-IR, H-1 NMR, C-13 NMR, ESI-MS and Single crystal X-ray analysis (4a). All the final scaffolds have been screened for antibacterial and antioxidant activities. Also their antitubercular activity against Mycobacterium tuberculosis H37RV was screened. (C) 2016 The Authors. Published by Elsevier B.V. on behalf of King Saud University.

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 117977-21-6 is helpful to your research. Name: 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, molecular formula is C18H21N3O2S, belongs to pyridine-derivatives compound, is a common compound. In a patnet, author is Lapointe, Sebastien, once mentioned the new application about 117977-21-6, SDS of cas: 117977-21-6.

Nickel(II) Complexes with Electron-Rich, Sterically Hindered PNP Pincer Ligands Enable Uncommon Modes of Ligand Dearomatization

We report the reactivity and characterization of hydride, methyl, and bromo Ni-II complexes with a new class of electron-rich and sterically hindered PNP pincer ligands, Me4PNPR (R = Pr-i, Bu-t), in which a classical metal-ligand cooperative mode of reactivity via CH2 arm deprotonation is blocked by methylation. This enables new, uncommon modes of PNP ligand dearomatization that involve reactivity in the para position of the pyridine ring. In particular, the reduction of [(Me4PNPiPr) (NiMe)-Me-II]B(Ar-F)(4) with KC8 leads to the formation of a new C-C bond via dimerization of two complexes through the para position. This reactivity stands in sharp contrast to the previously reported bromo or chloro complexes, where stable Ni-I halogen moieties are formed. Computational analysis showed a greater propensity for ligand-centered radical formation for the presumed intermediate one-electron-reduced species. UV-induced homolysis of the Ni-II-Me bond in [(Me4PNPiPr) (NiMe)-Me-II]B(Ar-F)(4) leads to the formation of a Me radical detected by radical traps and Ni(I )intermediates that can be trapped in the presence of halide ions to give previously characterized, stable Ni-I halogen complexes. In addition, treatment of the bromo complexes [(Me4PNPR)(NiBr)-Br-II]BPh4 with a powerful hydride source, LiBEt3H, leads to the reduction of the pyridine ring and the formation of Ni-II complexes with an anionic amide donor reduced pincer ligand, although aromatic Ni-II hydride complexes could also be obtained with a weaker hydride source. We have observed that steric bulk at the phosphine donors controls the reactivity of the resulting Ni(II)H( )complexes. While t-Bu-substituted [(Me4PNPtBu) (NiH)-H-II]Y(Y=BPh4, B(Ar-F)(4)) does not react with O-2, the less sterically hindered Pr-i-substituted [(Me4PNPiPr)(NiH)-H-II]Y reacts instantaneously to give an unstable superoxide adduct that can be observed by EPR.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Chemistry is an experimental science, Formula: C18H21N3O2S, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, molecular formula is C18H21N3O2S, belongs to pyridine-derivatives compound. In a document, author is Zhou, Qiang.

A novel 3D-printable hydrogel with high mechanical strength and shape memory properties

The three-dimensional (3D)-printing of hydrogels with excellent mechanical properties has attracted extensive attention owing to their potential applications in many fields. Through the photoinitiated copolymerization of methacrylic acid (MAAc) and N-(pyridin-2-yl)acrylamide (NPAM) in dimethylsulfoxide (DMSO), a copolymer solution was prepared; it was then 3D printed at 70 degrees C followed by solvent replacement of DMSO with water at 25 degrees C, and a novel 3D-printed tough hydrogel was prepared. In the presence of water, NPAM could undergo multi-fold hydrogen bonding with MAAc. Thus, the hydrogen bonding is strengthened and stabilized by the hydrophobic alpha-methyl of MAAc and the pyridine N-heterocycle of NPAM, meaning that the modules of the hydrogel can be up to five times stronger than the original organogels. The swelling or shrinkage of the gel is negligible during solvent replacement and the resultant hydrogel exhibits excellent mechanical properties, with an elastic modulus of 1.8-66 MPa, a tensile fracture stress of 2.2-6.3 MPa, a fracture strain of 360-570% and a fracture energy of 0.5-7.2 kJ m(-2). In addition, owing to the dynamic nature and temperature sensitivity of the hydrogen bonds, the hydrogel also exhibited fast self-recovery abilities and temperature activated shape memory properties. In particular, the hydrogen-bonding hydrogel could be quickly degraded and recovered by adjusting the pH, which allowed convenient recycling of the hydrogels. Our experimental results indicated that the combination of a 3D-printing technique and solvent replacement may provide a novel and effective method to obtain 3D-printed hydrogels with high mechanical strength and shape recovery properties, fostering their use in a number of fields such as soft robots, implant devices, tissue engineering and other environment friendly materials.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 117977-21-6. Formula: C18H21N3O2S.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Reference of 117977-21-6, Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. 117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, SMILES is COCCCOC1=C(C(=NC=C1)CSC2=NC3=C([NH]2)C=CC=C3)C, belongs to pyridine-derivatives compound. In a article, author is Li, Chifeng, introduce new discover of the category.

Ligand-Directed Approach in Polyoxometalate Synthesis: Formation of a New Divacant Lacunary Polyoxomolybdate [gamma-PMo10O36](7-)

A new ligand-directed approach for synthesizing lacunary polyoxomolybdates in organic solvents, which afforded an unprecedented lacunary polyoxomolybdate, is presented by Chifeng Li, Kazuya Yamaguchi, Kosuke Suzuki in their Communication (DOI: 10.1002/anie.202016642). By controlling the equilibrium of lacunary polyoxomolybdate ([alpha-PMo9O34](9-)) with pyridine molecules in N,N-dimethylacetamide, a selective structure transformation delivered the new lacunary polyoxomolybdate [gamma-PMo10O36](7-).

Reference of 117977-21-6, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 117977-21-6.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Application of 117977-21-6, As an important bridge between the micro and macro material world, chemistry is one of the main methods and means for humans to understand and transform the material world. 117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, SMILES is COCCCOC1=C(C(=NC=C1)CSC2=NC3=C([NH]2)C=CC=C3)C, belongs to pyridine-derivatives compound. In a article, author is Moses, Isaiah A., introduce new discover of the category.

Structural and electronic properties of layered nanoporous organic nanocrystals

In this work, we present the optimized geometric stacking of several layered nanoporous organic nanocrystals (NONs) and the stacking effect on their electronic structure. Hexagonal layered structures, C12H6-h2D, B6N6H6-h2D and C6N6-h2D are built from aromatic organic molecular units benzene, borazine and 1,3,5-triazine, respectively while oblique structures, C10N2H4-o2D, C8N4H2-o2D, C10P2H4-o2D and C10As2H4-o2D, are built from pyridine, 1,3-diazine, phosphinine and arsinine, respectively. Our density functional theory calculations show stacking energy profiles of NONs that are similar to graphene in both the stand-alone and bulk C12H6-h2D and B6N6H6-h2D structures while the rest of the studied layered materials deviate from the perfect AB stacking. The number of layers as well as the stacking configuration significantly influence the electronic properties of these materials. Indirect to direct band gap crossovers from the bulk to monolayers are observed in all of the NONs except in C6N6-h2D which exhibits a direct band gap in both the monolayer, isolated few-layers, and bulk. Furthermore, it is observed that the electronic nature of C10As2H4-o2D changes from a semiconducting character in the isolated monolayer to a metallic character in the bulk. The porous nature and the stability of these layered NONs combined with the electronic properties observed in this work point at them as valuable materials for potential applications in nanoelectronics and gas separation membranes, as well as deep ultraviolet optoelectronics and laser devices.

Application of 117977-21-6, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about 117977-21-6 is helpful to your research.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. Safety of 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, 117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, SMILES is COCCCOC1=C(C(=NC=C1)CSC2=NC3=C([NH]2)C=CC=C3)C, in an article , author is Das, Amal, once mentioned of 117977-21-6.

Energetically significant nitrile center dot center dot center dot nitrile and unconventional C-H center dot center dot center dot pi(nitrile) interactions in pyridine based Ni(II) and Zn(II) coordination compounds: Antiproliferative evaluation and theoretical studies

Two new coordination compounds viz. [Ni(2,6-PDC)(Hdmpz)(H2O)(2)]center dot H2O (1) and [Zn(3-CNpy)(2)Cl-2] (2) (2,6-PDC = 2,6-pyridinedicarboxylate, Hdmpz = 3,5-dimethylpyrazole, 3-CNpy = 3-cyanopyridine) have been synthesized and characterized using elemental analysis, thermogravimetric analysis, electronic, infrared spectroscopy and single crystal X-ray diffraction techniques. Crystal structure analyses reveal the presence of supramolecular assemblies involving interesting dimers with unconventional contacts in the compounds. DFT (Density Functional Theory) calculations on the supramolecular dimers in the crystal structure of 1 reveal that the sum of contributions of anion-pi, pi-pi and other long range interactions due to the approximation of the bulk monomers is energetically significant. Molecular Electrostatic Potential (MEP) surface and Quantum Theory of Atoms in Molecules (QTAIM) analyses on the interesting supramolecular dimers of the crystal structures of 2 reveal the presence of unconventional anion center dot center dot center dot pi contacts involving coordinated chlorido ligands and C-H center dot center dot center dot pi(nitrile) interactions involving the pi-system of the nitrile moiety of 3-cyanopyridine. Remarkably, Atoms in Molecules analysis also confirms the existence of energetically significant unconventional anti-parallel nitrile center dot center dot center dot nitrile interaction in the crystal structure of 2. Cell cytotoxicity of the compounds performed in Dalton’s lymphoma (DL) malignant cancer cell line showed effective potency with negligible cytotoxicity in normal cells (similar to 12%). It is interesting that compound 1has excellent cytotoxic potency with IC50 closer to cisplatin and can bind different biological targets with similar signalling pathways. Structure activity relationship (SAR) analyses of 1 and 2 based on pharmacophore modelling reveal that the molecular features associated with the structures of the compounds play important role in the biological activities. (C) 2020 Elsevier B.V. All rights reserved.

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 117977-21-6, you can contact me at any time and look forward to more communication. Safety of 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Electric Literature of 117977-21-6, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, SMILES is COCCCOC1=C(C(=NC=C1)CSC2=NC3=C([NH]2)C=CC=C3)C, belongs to pyridine-derivatives compound. In a article, author is Han, Shunyu, introduce new discover of the category.

Hierarchical Mg/ZSM-5 catalysts for methanol-to-propylene reaction via one-step acid treatment

One-step acid treatment for template- and solvent-free synthesized NaZSM-5 was developed to obtain hierarchical HZSM-5. Hierarchical Mg/ZSM-5 was obtained by the incipient impregnation method, which further increased the propylene yield of the methanol-to-propylene (MTP) reaction. The physicochemical properties of the samples were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), N-2 adsorption-desorption, pyridine adsorption-IR (Py-IR) and NH3 temperature-programmed desorption (NH3-TPD). The results indicated that one-step acid treatment (250 degrees C, 12 h) could increase the SiO2/Al2O3 molar ratio from 29.43 to 53.33 and maintain the well-distributed state of acid sites. The blocked pore structure was opened to introduce additional mesoporosity. Additionally, NaZSM-5 was synchronously converted to HZSM-5, thereby avoiding ion-exchange procedures. Synchronization of dealumination, desodiation and introduction of the mesoporous structure was achieved in one step, providing a good matrix for further impregnation with Mg species. The obtained hierarchical Mg/ZSM-5 (0.3 M-MgO) showed low diffusion hindrance and reduction in external surface acid sites (especially Bronsted acid sites), affording high propylene selectivity (53.34%) and good resistance to carbon deposition (similar to 0.77%) in the MTP reaction. [GRAPHICS] .

Electric Literature of 117977-21-6, One of the oldest and most widely used commercial enzyme inhibitors is aspirin, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 117977-21-6.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Chemistry can be defined as the study of matter and the changes it undergoes. You¡¯ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology. 117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, molecular formula is , belongs to pyridine-derivatives compound. In a document, author is Siegel, David, Recommanded Product: 117977-21-6.

A redox-mediated conformational change in NQO1 controls binding to microtubules and alpha-tubulin acetylation

The localization of NQO1 near acetylated microtubules has led to the hypothesis that NQO1 may work in concert with the NAD(+)-dependent deacetylase SIRT2 to regulate acetyl alpha-tubulin (K-40) levels on microtubules. NQO1 catalyzes the oxidation of NADH to NAD + and may supplement levels of NAD(+) near microtubules to aid SIRT2 deacetylase activity. While HDAC6 has been shown to regulate the majority of microtubule acetylation at K-40, SIRT2 is also known to modulate microtubule acetylation (K-40) in the perinuclear region. In this study we examined the potential roles NQO1 may play in modulating acetyl alpha-tubulin levels. Knock-out or knock-down of NQO1 or SIRT2 did not change the levels of acetyl alpha-tubulin in 16HBE human bronchial epithelial cells and 3T3-L1 fibroblasts; however, treatment with a mechanism-based inhibitor of NQO1 (MI2321) led to a short-lived temporal increase in acetyl alpha-tubulin levels in both cell lines without impacting the intracellular pools of NADH or NAD(+). Inactivation of NQO1 by MI2321 resulted in lower levels of NQO1 immunostaining on microtubules, consistent with redox-dependent changes in NQO1 conformation as evidenced by the use of redox-specific, anti-NQO1 antibodies in immunoprecipitation studies. Given the highly dynamic nature of acetylation-deacetylation reactions at alpha-tubulin K-40 and the crowded protein environment surrounding this site, disruption in the binding of NQO1 to microtubules may temporally disturb the physical interactions of enzymes responsible for maintaining the microtubule acetylome.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 117977-21-6, in my other articles. Recommanded Product: 117977-21-6.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, SMILES is COCCCOC1=C(C(=NC=C1)CSC2=NC3=C([NH]2)C=CC=C3)C, belongs to pyridine-derivatives compound. In a document, author is Malpani, Sakshi Kabra, introduce the new discover, SDS of cas: 117977-21-6.

Green, efficient and economical coal fly ash based phosphomolybdic acid catalysts: preparation, characterization and application

Cost-effective, efficient and green solid acid catalysts have been synthesized by incipient wetness impregnation of various weight fractions of phosphomolybdic acid (5, 10, 15 and 25 wt. %) on mechanically and thermally activated coal fly ash. N-2 adsorption-desorption, XRD, FT-IR, SEM, SEM-EDX, TEM, TGA, UV-Vis DRS, solid state P-31 MAS NMR were used for characterization of as synthesized catalysts. Catalytic active sites were developed on inert surface of coal fly ash by using various activation techniques whose performance was assessed over a series of acylation of various aliphatic alcohols. For rapid and higher catalytic activity, reactions were conducted in microwave heating mode. Impregnation of phosphomolybdic acid generates Lewis acidic sites on coal fly ash surface as inferred by pyridine adsorbed FT-IR studies which were then utilized in acylation reactions. Various reaction parameters like weight fraction of catalysts, molar ratio of reactants, time, temperature, etc. were optimized for attaining highest conversion %. The catalyst with 15 wt. % of phosphomolybdic acid was found to be more efficient and could be recycled up to five reaction cycles with analogous conversion %. Negligible leaching of catalyst was confirmed by hot filtration test. This work suggests an alternative approach for valorisation of industrial solid waste, coal fly ash in development of innovative, economical solid catalysts. [GRAPHICS] .

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 117977-21-6 is helpful to your research. SDS of cas: 117977-21-6.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem