Category: 108-30-5

Related Products of 108-30-5, 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. 108-30-5, Name is Dihydrofuran-2,5-dione, SMILES is O=C(CC1)OC1=O, belongs to tetrahydrofurans compound. In a article, author is Kim, Min Cheol, introduce new discover of the category.

Complementary Genomic, Bioinformatics, and Chemical Approaches Facilitate the Absolute Structure Assignment of lonostatin, a Linear Polyketide from a Rare Marine-Derived Actinomycete

A new linear type-1 polyketide, ionostatin (1), has been fully defined using a combined genomic and bioinformatics approach coupled with confirmatory chemical analyses. The 41 carbon-containing polyether is the product of the 101 kbp ion biosynthetic cluster containing seven modular type-1 polyketide synthases. Ionostatin is composed of 15 chiral centers that were proposed using the stereospecificities installed by the different classes of ketoreductases and enoylreductases and confirmed by rigorous NMR analyses. Incorporated into the structure are two tetrahydrofuran rings that appear to be the product of stereospecific epoxidation, followed by stereospecific ring opening and cyclization. These transformations are proposed to be catalyzed by conserved enzymes analogous to those found in other bacterial-derived polyether biosynthetic clusters. Ionostatin shows moderate cancer cell cytotoxicity against U87 glioblastoma and SKOV3 ovarian carcinoma at 7.4 mu g/mL.

Related Products of 108-30-5, 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 108-30-5.

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. Computed Properties of C4H4O3, 108-30-5, Name is Dihydrofuran-2,5-dione, SMILES is O=C(CC1)OC1=O, in an article , author is Kang, Houng, once mentioned of 108-30-5.

Nickel-Catalyzed Vinylidene Insertions into O-H Bonds

A (pybox)Ni catalyst (where pybox = pyridine-bis(oxazoline)) promotes the reductive cyclization of beta-hydroxy 1,1-dichloroalkenes to form 2,3-dihydrofurans. The substrates for this reaction are conveniently prepared by an aldol addition, followed by one-carbon homologation. Chiral substrates are accessible in highly enantioenriched form, allowing for the synthesis of stereochemically complex 2,3,4-trisubstituted products. Mechanistic studies support a vinylidene O-H insertion rather than a C-O cross-coupling pathway.

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 108-30-5, you can contact me at any time and look forward to more communication. Computed Properties of C4H4O3.

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

Related Products of 108-30-5, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 108-30-5, Name is Dihydrofuran-2,5-dione, SMILES is O=C(CC1)OC1=O, belongs to tetrahydrofurans compound. In a article, author is Hussain, S. G. Mohammed, introduce new discover of the category.

Steric effect in the formation of hydrogen bonded complexes of isopropylamine with alicyclic ethers by ultrasonic and DFT approach

Experimental (acoustical) and theoretical (DFT) analyses have been undertaken to unravel the possibility of hydrogen bonded complexes of isopropylamine (IPA) with two industrially important cyclic ethers, tetrahydrofuran (THF) and 1,4 dioxane (DIOX) in n – hexane at 303.15 K and at atmospheric pressure. The trend in acoustical and excess parameters with concentration revealed the dominance of structure breaking behavior of like molecules of solute components and formation of intermolecular H-bonding between IPA and ethers in the two ternary systems at room temperature. The data obtained through DFT studies further support the existence of intermolecular H-bond between amine and ethers. The strength of interactions has been assessed from the formation constants (K) determined by acoustic method and interaction energies by DFT respectively. The reduced density gradient (RDG) and non-covalent interaction (NCI) plots clearly exhibit the presence of intermolecular interactions in the twosystems. The stability of these complexes and the strength of the interactions are explained with the structure of ether. Comparison of K and interaction energy values in the present study with those obtained in n-propylamine interactions with ethers showed steric effect in the formation of complex of IPA with the two ethers. (c) 2020 Elsevier B.V. All rights reserved.

Related Products of 108-30-5, 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 108-30-5.

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

Synthetic Route of 108-30-5, 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. 108-30-5, Name is Dihydrofuran-2,5-dione, SMILES is O=C(CC1)OC1=O, belongs to tetrahydrofurans compound. In a article, author is Olonisakin, Kehinde, introduce new discover of the category.

Effect of TDI-Assisted Hydrophobic Surface Modification of Microcrystalline Cellulose on the Tensile Fracture of MCC/PLA Composite, and Estimation of the Degree of Substitution by Linear Regression

Microcrystalline cellulose (MCC) was modified using toluene-2,4-diisocyanate (TDI) in tetrahydrofuran (THF). The reaction was set up for 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, and 24 h at 75 degrees C. The study was aimed at hydrophobic modification of microcrystalline cellulose (MCC) to improve its dispersion in PLA matrix. Data from the elemental analysis were used to develop a statistical model to predict the degree of substitution (DS) of the OH on the surface of the MCC using both the water contact angle (WCA) and the time of carbamation as the independent variables. Composite was fabricated at 1%, 2%, 3%, 4%, and 5% fiber loading. Fourier transformed infrared spectroscopy was used to characterize the MCC and to confirm the successful graft of TDI to the MCC surface. The morphology and elemental analysis of the modified samples were examined with SEM-EDX. The samples’ wettability was analyzed with a contact angle meter to measure the water contact angle (WCA). The tensile properties of composites were analyzed on a universal testing machine. The result showed that, after 1 h of carbamation, the minimum DS recorded was 0.11, and the maximum DS after 24 h was 0.16. The SEM revealed that the modified MCC had homogeneous dispersion in the polymer matrix. At 3% fiber loading, the tensile strength (TS) and elongation were at a maximum and had improvements of 80.67% and 79.44% as compared to neat PLA. The fractured tensile surface from SEM analysis showed that surface modification enhanced fiber-matrix adhesion and significantly improved the composite’s strength and toughness. The proposed model that was developed in this study had a coefficient of determination (R-2) of 93% to show that the model has a near-perfect goodness of fit and can well be an effective approach to predict the DS of OH from WCA and the time of reaction at similar or the same reaction conditions.

Synthetic Route of 108-30-5, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 108-30-5.

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

Application of 108-30-5, 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. 108-30-5, Name is Dihydrofuran-2,5-dione, SMILES is O=C(CC1)OC1=O, belongs to tetrahydrofurans compound. In a article, author is Yaragani, Muralikrishna, introduce new discover of the category.

Design and synthesis of novel tetrahydrofuran cyclic urea derivatives as androgen receptor antagonists

In order to improve the antiproliferative activity of androgen receptor (AR) antagonists, which used clinically for the treatment of prostate cancer that is a major cause of male death in worldwide, we report the design and synthesis of a series of tetrahydrofuran cyclic urea-based non-steroidal small molecule AR antagonists and exhibit potent AR antagonistic activity. These molecules with higher stereochemical aspects have been achieved by changing the hydantoin analogue antiandrogens to 4-(2-oxohexahydro-1H-furo[3,4-d] imidazol-1-yl)-2-(trifluoromethyl)benzonitrile analogues. Here, the thio-hydantoin pharmacophore of the recently reported antagonists is replaced by tetrahydrofuran cyclic urea. The antiproliferative properties of these molecules have been evaluated against androgen-dependent (LNCaP) cell line. Among the reported molecules, 4-(2-oxohexahydro-1H-furo[3,4-d]imidazol-1-yl)-2-(trifluoromethyl)benzonitrile (AR04) showed significantly improved in vitro activity, IC50= 3.926 mu M. Molecular structure-activity relationship studies confirm that the oxetane analogueAR04is distinct from other synthesized AR antagonists. These results have suggested thatAR04exhibiting their potential as a lead compound for the alternative treatment of prostate cancer.

Application of 108-30-5, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 108-30-5 is helpful to your research.

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

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. 108-30-5, Name is Dihydrofuran-2,5-dione, molecular formula is C4H4O3. In an article, author is Chen, Yao,once mentioned of 108-30-5, Recommanded Product: 108-30-5.

One-Pot Synthesis of the Biofuel 5-Ethoxymethylfurfural from Carbohydrates Using a Bifunctional Catalyst Prepared through a Pickering HIPE Template and Pore-Filled Strategy

As a very promising biofuel or fuel additive, the synthesis of 5-ethoxymethylfurfural (EMF) directly from renewable carbohydrates is an important biomass transformation process. Herein, a novel bifunctional catalyst has been successfully synthesized via a Pickering high internal phase emulsion (HIPE) template and pore-filled strategy and employed for the production of EMF from glucose in a one-pot manner. Catalytic results indicated that the grafted Cr3+ by the atom transfer radical polymerization (ATRP) method smoothly processed the isomerization of glucose to intermediate fructose and that the accessible -SO3H and Cr3+ active sites coexisted in the obtained bifunctional catalyst possessing synergistic effects. A high EMF yield of 48.1% was achieved under optimal reaction conditions in an ethanol/tetrahydrofuran (THF) medium. Besides, employing inulin, sucrose, cellobiose, maltose, and starch as the starting materials excellent EMF yields were also obtained over the developed bifunctional catalyst. This study offers new insights into the design of functional catalysts anchoring desirable active sites, and also highlights their applications for biomass transformation.

Interested yet? Keep reading other articles of 108-30-5, you can contact me at any time and look forward to more communication. Recommanded Product: 108-30-5.

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

Application of 108-30-5, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 108-30-5, Name is Dihydrofuran-2,5-dione, SMILES is O=C(CC1)OC1=O, belongs to tetrahydrofurans compound. In a article, author is Mermat, Nihad, introduce new discover of the category.

Original Mesogenic Citronellol-Based Stationary Phase for Both Normal- and Reversed-Phase HPLC Modes: Properties and Applications

In this work, the synthesis, characterization and chromatographic performance of a silica material chemically bonded with a liquid crystal based on terminal citronellol for HPLC separation were investigated. This bonded liquid crystal stationary phase denoted as LC-LCC(8)resulted from the grafting of a mesogenic carboxylic acid, 3 ‘-((3,7-dimethyloct-6-en-1-y1)oxy)-[1,1 ‘-biphenyl]-4-carboxylic acid (LCC8), on 4-(1,1-dimethyldisiloxanyl)butan-1-amine. LCC(8)was previously synthesized and characterized by proton NMR, and a nematic mesophase at 127 degrees C was confirmed by differential scanning calorimetry and microscopy. The resulting stationary phase LC-LCC(8)was characterized by using diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy and elemental analysis. The granulometric distribution was evaluated by scanning electron microscopy (SEM) before and after grafting. An analytical column (150 mm x 2.1 mm x 5 mu m) was packed with the stationary phase for the chromatographic study. The chromatographic behaviour of the stationary phase was first characterized using the Tanaka test, exhibiting an exceptionally high shape selectivity (alpha(T/O) = 3.9). In normal-phase mode, using a 92/8 cyclohexane/tetrahydrofuran (THF)(v/v)mixture as the mobile phase, the isomeric mixture (Z and E) of crotamiton was well separated. In reversed-phase mode, good selectivity was observed towards organic pollutants [polycyclic aromatic hydrocarbons (PAHs)] and pharmaceutical compounds (xanthines, steroids and antihistamines). The new bonded phase showed satisfactory results both in normal- and reversed-phases modes except in terms of peak shape. The temperature effect on the selectivity and resolution of LC-LCC(8)was estimated by injecting different isomers at various temperatures ranging from 293 to 333 K, demonstrating an improved resolution of solutes at high temperatures, which was probably due to a change in orientation order of the grafted ligands.

Application of 108-30-5, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 108-30-5 is helpful to your research.

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

Synthetic Route of 108-30-5, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 108-30-5, Name is Dihydrofuran-2,5-dione, SMILES is O=C(CC1)OC1=O, belongs to tetrahydrofurans compound. In a article, author is Morinaga, Hisatoyo, introduce new discover of the category.

Synthesis of polymers via cationic ring-opening polymerization using (NH4)(3)PW12O40-SiO(2)composite catalyst

Composite catalyst of heteropolyacid ammonium salt, (NH4)(3)PW12O40, and SiO(2)was prepared by sol-gel method. The resultant catalyst ((NH4)(3)PW12O40-SiO2, 3.38wt%) having W/Si molar ratio of 2/8 enabled to proceed ring-opening polymerizations of tetrahydrofuran (THF), epsilon-caprolactone (CL), and glycidyl phenyl ether (GPE) to give the corresponding poly(THF), poly(CL), and poly(GPE) having number-average molecular weights (M-n) of 6610, 4010, and 2370 with polydispersity index (M-w/M-n) of 1.57, 1.36, and 1.49 in 24%, 88%, and 59% yields, respectively. Matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS) spectra of poly(CL) and poly(GPE) exhibited that Bronsted acid induced from (NH4)(3)PW12O40-SiO(2)is the only one species that initiates the polymerization.

Synthetic Route of 108-30-5, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 108-30-5.

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

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 108-30-5, Name is Dihydrofuran-2,5-dione, formurla is C4H4O3. In a document, author is Kato, Shota, introducing its new discovery. SDS of cas: 108-30-5.

Total synthesis and complete configurational assignment of amphirionin-2

Amphirionin-2 is a linear polyketide metabolite that exhibits potent and selective cytotoxic activity against certain human cancer cell lines. We disclose herein the first total synthesis of amphirionin-2 and determination of its absolute configuration. Our synthesis featured an extensive use of cobalt-catalyzed Mukaiyama-type cyclization of gamma-hydroxy olefins for stereoselective formation of all the tetrahydrofuran rings found in the natural product, and a late-stage Stille-type coupling for convergent assembly of the entire carbon backbone. Four candidate diastereomers of amphirionin-2 were synthesized in a unified, convergent manner, and their spectroscopic/chromatographic properties were compared with those of the authentic material. The present study culminated in the reassignment of the C5/C7 relative configuration, assignment of the C12/C18 relative configuration, and determination of the absolute configuration of amphirionin-2.

If you are hungry for even more, make sure to check my other article about 108-30-5, SDS of cas: 108-30-5.

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

Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 108-30-5, Name is Dihydrofuran-2,5-dione, SMILES is O=C(CC1)OC1=O, belongs to tetrahydrofurans compound. In a document, author is Mrowka, Jan, introduce the new discover, Application In Synthesis of Dihydrofuran-2,5-dione.

Poly(methylvinylsiloxane)-Based High Internal Phase Emulsion-Templated Materials (polyHIPEs)-Preparation, Incorporation of Palladium, and Catalytic Properties

Poly(methylvinylsiloxane) (V-3 polymer) obtained by kinetically controlled anionic ring-opening polymerization of 1,3,5-trimethy1-1,3,5-trivinylcyclotrisiloxane was cross-linked with various amounts of 1,3,5,7-tetramethylcyclotetrasiloxane (D-4(H)) in w/o high internal phase emulsions (HIPEs). PolyHIPEs thus prepared differed in the polymer cross-linking degree, which affected their porous morphology and total porosity. The obtained V-3 polymer-based polyHIPEs were applied as matrices for the incorporation of Pd from the Pd(OAc)(2) solution in tetrahydrofuran. This process involved the conversion of Si-H groups remaining in the polymer networks and resulted in the formation of crystalline, metallic Pd in the systems. Mean sizes of the generated Pd crystallites were lower in polyHIPEs of higher than in those of lower polymer cross-linking degrees and porosities (similar to 5 nm vs similar to 8 nm, respectively). The Pd-containing polyHIPEs showed activity in catalytic hydrogenation of the triple carbon-carbon bond in phenylacetylene giving the unsaturated product, styrene with a selectivity of ca. 80%. To the best of our knowledge, this is the first work devoted to polysiloxane-based polyHIPEs with dispersed metallic particles.

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 108-30-5 is helpful to your research. Application In Synthesis of Dihydrofuran-2,5-dione.

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