Category: 149809-43-8

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels. 149809-43-8, Name is ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate, molecular formula is C21H21F2N3O4S. In an article, author is Sato, Ryoya,once mentioned of 149809-43-8, Product Details of 149809-43-8.

Formation of Three-Dimensional Electronic Networks Using Axially Ligated Metal Phthalocyanines as Stable Neutral Radicals

Organic pi-radical crystals are potential single-component molecular conductors, as they involve charge carriers. We fabricated new organic pi-radical crystals using axially ligated metal phthalocyanine anions ([M-III(Pc)L-2](-)) as starting materials. Electrochemical oxidation of [M-III(Pc)L-2](-)afforded single crystals of organic pi-radicals of the type M-III(Pc)Cl-2 center dot THF (M = Co or Fe, THF = tetrahydrofuran), where the pi-conjugated macrocyclic phthalocyanine ligand is one-electron oxidized. The X-ray crystal structure analysis revealed that M-III(Pc)Cl-2 formed three-dimensional networks with pi-pi overlaps. The electrical resistivities of Co-III(Pc)Cl-2 center dot THF and Fe-III(Pc)Cl-2 center dot THF at room temperature along thea-axis were 6 x 10(2)and 6 x 10(3) Omega cm, respectively, and were almost isotropic, meaning that M-III(Pc)Cl-2 center dot THF had three-dimensional electronic systems.

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Reference:
Tetrahydrofuran – Wikipedia,
,Tetrahydrofuran | (CH2)3CH2O – PubChem

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. SDS of cas: 149809-43-8, 149809-43-8, Name is ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate, SMILES is O=S(C1=CC=C(C)C=C1)(OC[C@H]2CO[C@](C3=CC=C(F)C=C3F)(CN4N=CN=C4)C2)=O, in an article , author is Li, Zi-Han, once mentioned of 149809-43-8.

Breaking the axiality of pentagonal-bipyramidal dysprosium(iii) single-molecule magnets with pyrazolate ligands

A range of pyrazolate-based ligands have been used to balance the multidentate-chelating feature and the magnetic axiality in destroyed pentagonal-bipyramidal (DPB) dysprosium(iii) single-molecule magnets (SMMs). This family of complexes are air-stable and share the general formulae of [(DyXX2)-X-1(L-eq)(5)][BPh4], where X-1 and X-2 are the anionic axial ligands, including pyrazolate-based ligands and chloride; L-eq is the equatorial solvent molecule such as tetrahydrofuran (THF), pyridine (py) and thiazole (NS). Compared to the prototype PB SMMs, the bidentate-chelating features of the pyrazolate ligands show, albeit slow magnetic relaxation behavior, a much smaller energy barrier for magnetization reversal (U-eff). Static electronic calculation shows that the magnetic axiality above the ground m(J) = +/- 15/2 states has been much reduced, leading to the mixing of other states at higher levels. Nevertheless, this systematic study reveals that the variation of the substituents on the pyrazolate ligands and the replacement of planar solvents are effective at influencing the magnetic relaxation behavior. We found that the chloride coordinating mono-pyrazolate complexes, such as [(DyXCl)-Cl-1(THF)(5)][BPh4] (X-1 = 3-(trifluoromethyl)pyrazole (tfpz) 1, X-1 = 3-methylpyrazole (Mepz) 2, X-1 = 3-isopropyl-1H-pyrazole (Iprpz) 3, X-1 = 3,5-dimethylpyrazole (Me(2)pz) 4, X-1 = 3,5-diisopropylpyrazole (Ipr(2)pz) 5, and X-1 = pyrazole (pz) 6, generally show lower U-eff, while bi-pyrazolate complexes, such as [Dy(tfpz)(2)(THF)(5)][BPh4] 7, [Dy(pz)(2)(THF)(5)][BPh4] 8, [Dy(pz)(2)(py)(5)][BPh4]center dot 2py 9 and [Dy(pz)(2)(NS)(5)][BPh4] 10, show higher U-eff. Among them, 8 shows the largest U-eff of 521(8) K and a comparable open hysteresis temperature of similar to 5 K (at a field sweeping rate of 12 Oe s(-1)) with 9 and 10. The enhanced blocking temperature for 8 is different from that for the PB Dy(iii) SMMs in which the py ligand can cause a much higher hysteresis temperature than the one coordinated with THF due to the aromatic pi-pi interactions, indicating that the bis-bidentate-chelating Dy(iii) ion is rigid enough to reduce the influence from the equatorial ligands. Moreover, substitution with electron-withdrawing groups such as the -CF3 group reduces U-eff prominently. Such a clear magnetostructural correlation in Dy(iii) SMMs is fundamentally important, indicating that a subtle balance between magnetic axiality and molecular rigidity is critical to design high-performance Dy(iii) SMMs.

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Reference:
Tetrahydrofuran – Wikipedia,
,Tetrahydrofuran | (CH2)3CH2O – PubChem

Chemistry is an experimental science, Safety of ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 149809-43-8, Name is ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate, molecular formula is C21H21F2N3O4S, belongs to Tetrahydrofurans compound. In a document, author is Gundekari, Sreedhar.

In situ Generated Ru(0)-HRO@Na-beta From Hydrous Ruthenium Oxide (HRO)/Na-beta: An Energy-Efficient Catalyst for Selective Hydrogenation of Sugars

A green process for the hydrogenation of sugars to sugar alcohols was designed in aqueous medium using hydrous ruthenium oxide (HRO) as a pre-catalyst supported on Na-beta zeolite. Under optimized reaction conditions, sugars such as xylose, glucose, and mannose converted completely to the corresponding sugar alcohols xylitol, sorbitol, and mannitol with 100% selectivity. The pre-catalyst (HRO) is converted in situ to active Ru(0) species during the reaction under H-2, which is responsible for the hydrogenation. The catalyst was recyclable up to five cycles with no loss in activity. The reduction of HRO to the active Ru(0) species is dependent on the reaction temperature and H-2 pressure. Ru(0) formation increased and consequently an increased hydrogenation of sugars was observed with an increase in reaction temperature and hydrogen pressure. Further, in situ generation of Ru(0) from HRO was assessed in different solvents such as water, methanol, and tetrahydrofuran; aqueous medium was found to be the most efficient in reducing HRO. This work further demonstrates the use of supported HRO as an efficient pre-catalyst for biomass-based hydrogenation reactions.

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 149809-43-8. Safety of ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate.

Reference:
Tetrahydrofuran – Wikipedia,
,Tetrahydrofuran | (CH2)3CH2O – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. The former is the study of compounds containing at least one carbon-hydrogen bonds. 149809-43-8, Name is ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate, molecular formula is C21H21F2N3O4S, belongs to Tetrahydrofurans compound, is a common compound. In a patnet, author is Wang, Fang, once mentioned the new application about 149809-43-8, Recommanded Product: 149809-43-8.

Multi-Stimuli Responsive Luminescent beta-Diketones and Difluoroboron Complexes with Heterocyclic Substituents

Emissive beta-diketones (bdks) and difluoroboron complexes (BF(2)bdks) exhibit multi-stimuli responsive luminescence, including solvatochromism, viscochromism, aggregation induced emission, thermal and mechanochromic luminescence, halochromism and pH sensing. In this study, a series of six-membered heterocycle-substituted (piperidine, morpholine, 1-methyl piperazine) bdk ligands and boron complexes were synthesized, and their luminescent properties were investigated. All the compounds exhibited red-shifted emission in more polar solvents due to intramolecular charge transfer as well as higher emission intensity in more viscous environments. In response to solubility changes in water/tetrahydrofuran mixtures, while the piperazine bdk ligand showed aggregation caused quenching, the piperidine and morpholine bdks displayed enhanced emission upon aggregation. In the solid state, all ligands exhibited mechanochromism. More dramatic halochromism was observed for the piperidine boron dye spin cast film. In solution, for the boron dyes under varying pH values (1-13), different protonated and deprotonated forms were analyzed according to the measured emission spectra.

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Reference:
Tetrahydrofuran – Wikipedia,
,Tetrahydrofuran | (CH2)3CH2O – PubChem

Related Products of 149809-43-8, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 149809-43-8, Name is ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate, SMILES is O=S(C1=CC=C(C)C=C1)(OC[C@H]2CO[C@](C3=CC=C(F)C=C3F)(CN4N=CN=C4)C2)=O, belongs to Tetrahydrofurans compound. In a article, author is Gong, Li, introduce new discover of the category.

A superhydrophobic and porous polymer adsorbent with large surface area

A superhydrophobic hypercrosslinked microporous polymer adsorbent, SHMP-1, with a water contact angle of 167 degrees and an oil contact angle < 3 degrees, was synthesized. SHMP-1 has a specific surface area of up to 2100 m(2) g(-1), higher than the largest one (i.e. 1618 m(2) g(-1)) reported for superhydrophobic materials. It is an amorphous polymer with a highly cross-linked structure of monomers linked by methylene, and consists of packed amorphous porous cells with pore channel widths of 5-19 angstrom. SHMP-1 can be stable up to 380 degrees C, and in organic solvents (e.g. ethanol, acetone, carbon tetrachloride, tetrahydrofuran and n-hexane), HCl (5 mol L-1) and NaOH (5 mol L-1) solution. This polymer could be a promising adsorbent for absorption of organic solvents with capacities ranging from 4-25 times its own weight and capturing CO2 with an adsorption capacity of up to 6.02 mmol g(-1) (273 K, 1 bar). Moreover, the CO2 adsorption capacity of SHMP-1 will not be decreased significantly (loss < 2.03%) by moisture even at a relative humidity of up to 90%, because of the surface superhydrophobicity. Related Products of 149809-43-8, 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 149809-43-8.

Reference:
Tetrahydrofuran – Wikipedia,
,Tetrahydrofuran | (CH2)3CH2O – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. HPLC of Formula: C21H21F2N3O4S, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 149809-43-8

IMPROVED PROCESS FOR THE PREPARATION OF ((3S,5R)-5-((1H-1,2,4-TRIAZOL-1-YL)METHYL)-5-(2,4-DIFLUOROPHENYL)TETRAHYDROFURAN-3-YL)METHYL-4-METHYLBENZENESULFONATE

The present invention relates to process for the preparation of ((3S,5R)-5-((lH-l,2,4- triazol- 1 -yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl-4-methylbenzene sulfonate compound of formula- 1 through novel intermediates. Further the said compound of formula- 1 is useful as a key intermediate for the preparation of Posaconazole.

If you are interested in 149809-43-8, you can contact me at any time and look forward to more communication. HPLC of Formula: C21H21F2N3O4S

Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem

Synthetic Route of 149809-43-8, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 149809-43-8, Name is ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate, molecular formula is C21H21F2N3O4S. In a Patent£¬once mentioned of 149809-43-8

Process for the Preparation of Triazole Antifungal Drug, Its Intermediates and Polymorphs Thereof

A process for the preparation of 4-[4-[4-[4-[[(3R,5R)-5-(2,4-difluorophenyl)tetrahydro-5-(1H-1,2,4-triazol-1-ylmethyl)-3-furanyl]methoxy]phenyl]-1-piperazinyl]phenyl]-2-[(1S,2S)-1-ethyl-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one compound of formula-1, its intermediates and polymorphs thereof. (I)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 149809-43-8. In my other articles, you can also check out more blogs about 149809-43-8

Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem

Related Products of 149809-43-8, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 149809-43-8, Name is ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate, molecular formula is C21H21F2N3O4S. In a Patent£¬once mentioned of 149809-43-8

Posaconazole impurity and its preparation and use (by machine translation)

The invention discloses posaconazole impurity, for example 4 c (wherein PG is a hydroxy protecting group); at the same time, also discloses a method of preparing these impurities and use thereof. (by machine translation)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Related Products of 149809-43-8. In my other articles, you can also check out more blogs about 149809-43-8

Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem

Related Products of 149809-43-8, 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, 149809-43-8, molcular formula is C21H21F2N3O4S, introducing its new discovery.

A preparation method of posaconazole (by machine translation)

The invention discloses a method for preparation of posaconazole. The invention provides a preparation method of posaconazole I, comprising the following steps: inorganic proton acid under the condition, the compound II hydrolytic reaction, I obtain the posaconazole. Preparation method of this invention simple and safe operation, without special equipment, heavy metal residues, less reaction by-product, high yield, high purity of the prepared product (chiral purity is greater than 99.90%; the related substance purity is greater than 99.50%, all impurity is less than 0.1%, the raw materials to achieve standard), low production cost, environment-friendly, and is suitable for industrial production. (by machine translation)

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 149809-43-8 is helpful to your research. Related Products of 149809-43-8

Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem

Reference of 149809-43-8, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 149809-43-8, Name is ((3R,5R)-5-((1H-1,2,4-Triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate,introducing its new discovery.

Design and synthesis of potential inhibitors of the ergosterol biosynthesis as antifungal agents

A series of azolylmethyloxolane derivatives with modified sterol side-chain structures, designed as potential dual functional inhibitors of cytochrome P450 14alpha-demethylase (14DM) and Delta24-sterol methyltransferase (24-SMT) based on the common characteristic features of 24-aminosterols and azole antifungal agents, were synthesized and evaluated for their antifungal activities and inhibitory activities of 14DM and 24-SMT. Among these compounds, imidazolylmethyloxolane derivatives 28a and 28b showed potent in vitro antifungal activities comparable to those of itraconazole. However, the in vitro bioactivities have not been linearly translated into in vivo protection data for some unknown reasons. Copyright (C) 2000 Elsevier Science Ltd.

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Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem