Category: 15833-61-1

15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol, belongs to tetrahydrofurans compound, is a common compound. Recommanded Product: (Tetrahydrofuran-3-yl)methanolIn an article, once mentioned the new application about 15833-61-1.

The present invention relates to compounds of general formula I, (I), wherein the groups R1, R2 and m are defined as in claim 1, which have valuable pharmacological properties, in particular bind to the GPR40 receptor and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.

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

Reference of 15833-61-1, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol, molecular formula is C5H10O2. In a Patent，once mentioned of 15833-61-1

Process for the preparation of 3-methyltetrahydrofuran

Disclosed is a process for the preparation of 3-methyltetrahydrofuran (MeTHF) from 3-(hydroxymethyl)tetrahydrofuran (HOMeTHF) by contacting HOMeTHF with hydrogen in the presence of an acidic, supported catalyst comprising a Group VIII metal.

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

Related Products of 15833-61-1, 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, 15833-61-1, molcular formula is C5H10O2, introducing its new discovery.

NEW ACETYL COENZYME A CARBOXYLASE (ACC) INHIBITORS AND USES IN TREATMENTS OF OBESITY AND DIABETES MELLITUS – 087

Field of the invention The present invention relates to Acetyl Coenzyme A Carboxylase (ACC) inhibitors, to processes for preparing such compounds, to pharmaceutical compositions containing them, to the use of such inhibitors and to methods for their therapeutic use, particularly in the treatments of obesity and diabetes mellitus.

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 15833-61-1 is helpful to your research. Related Products of 15833-61-1

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, Product Details of 15833-61-1, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol, molecular formula is C5H10O2

A production method of the dinotefuran (by machine translation)

The invention discloses a production method of the dinotefuran, comprises the following steps: the tetrahydrofuran methanol, toluene, triethylamine after stirring, to join the toluene sulfonyl chloride, steam heating reflux reaction, by adding water to stir layered, and distilled to remove the toluene […] a share intermediate A; methyl nitroguanidine, ethanol, methyl amine in the aqueous solution is added to the reaction kettle, dropping formaldehyde aqueous solution, after heating reaction, cooling crystallization, filtration and drying get intermediate B; the intermediate A, intermediate in DMF B and put into a reaction kettle, stirring and mixing of the latter adds by drops the liquid caustic soda, stirring after the temperature of the cooling to the room temperature, adding hydrochloric acid up stirring, then dichloromethane is used for extraction, concentration, cooling crystallization, filtering, drying get intermediate C; the intermediate C and urea added in a reaction kettle, adding isobutanol, insulation after the temperature of the cooling and filtering, after the water washing is obtained after drying. The invention has simple operation, the total high yield, low cost, environmental protection and pollution-free, and is suitable for industrial production. (by machine translation)

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

Application of 15833-61-1, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol,introducing its new discovery.

3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same.

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

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. COA of Formula: C5H10O2. Introducing a new discovery about 15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol

The Negative Ion Mass Spectra of Deprotonated Carbohydrates. Part 1. The Basic Hydroxymethyl-substituted Ring Systems

Tetrahydrofuran-2-methanol and tetrahydropyran-2-methanol are models for the basic ring systems of simple carbohydrates.These compounds deprotonate, in the gas phase, principally at the HO group.The major fragmentations of these systems involve competitive losses of H2O and CH2O.Labelling (18O and 2H), and product ion studies, indicate that proton transfer between the 3-position on the ring and -CH2O- yields a 3-anion which immediately ring opens.The ring opened alkoxide may undergo proton transfers which effectively make both of the oxygens equivalent.Other tetrahydrofuran- and tetrahydropyran-methanols also undergo ring cleavage: their negative ion spectra show subtle differences.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.COA of Formula: C5H10O2, you can also check out more blogs about15833-61-1

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

Related Products of 15833-61-1, 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. 15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol, molecular formula is C5H10O2. In a Patent£¬once mentioned of 15833-61-1

AMIDE COMPOUND AND USE THEREOF FOR PEST CONTROL

An amide compound represented by formula (I) has an excellent pest control effect. (In the formula, Y represents a 3-7 membered saturated heterocyclic ring which contains, as ring-forming component(s), one or more atoms or groups that are selected from the group consisting of an oxygen atom and -S(O)t-, the saturated heterocyclic ring may have one to three atoms or groups selected from group D and t represents 0 or the like; X represents a C1-C10 chain hydrocarbon group which may have one or more atoms or groups that are selected from group A, or the like; W represents -CR8- or the like; r represents 1 or the like; R1, R2, R3, R4, R5, R6, R7 and R8 may be the same or different and each represents a hydrogen atom or the like; and n represents 1 or the like.)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Related Products of 15833-61-1. In my other articles, you can also check out more blogs about 15833-61-1

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

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Quality Control of (Tetrahydrofuran-3-yl)methanol. Introducing a new discovery about 15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol

Electron-induced chemistry of alcohols

We studied dissociative electron attachment to a series of compounds with one or two hydroxyl groups. For the monoalcohols we found, apart from the known fragmentations in the 6-12 eV range proceeding via Feshbach resonances, also new weaker processes at lower energies, around 3 eV. They have a steep onset at the dissociation threshold and show a dramatic D/H isotope effect. We assigned them as proceeding via shape resonances with temporary occupation of sigma*O-H orbitals. These low energy fragmentations become much stronger in the larger molecules and the strongest DEA process in the compounds with two hydroxyl groups, which thus represent an intermediate case between the behavior of small alcohols and the sugar ribose which was discovered to have strong DEA fragmentations near zero electron energy [S. Ptasinska, S. Denifl, P. Scheier and T. D. Maerk, J. Chem. Phys., 2004, 120, 8505]. Above 6 eV, in the Feshbach resonance regime, the dominant process is a fast loss of a hydrogen atom from the hydroxyl group. In some cases the resulting (M – 1)- anion (loss of hydrogen atom) is sufficiently energy-rich to further dissociate by loss of stable, closed shell molecules like H2 or ethene. The fast primary process is state- and site selective in several cases, the negative ion states with a hole in the n O orbital losing the OH hydrogen, those with a hole in the sigmaC-H orbitals the alkyl hydrogen. the Owner Societies.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Quality Control of (Tetrahydrofuran-3-yl)methanol, you can also check out more blogs about15833-61-1

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

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Formula: C5H10O2, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 15833-61-1, name is (Tetrahydrofuran-3-yl)methanol. In an article£¬Which mentioned a new discovery about 15833-61-1

Hydrogenation of furfural to butanol and pentanols for renewable gasoline blendstocks

Butanols and pentanols can be prepared in high selectivity from furfural reduction in a catalyzed continuous hydrogenation process. The catalyst should have bifunctional activity with both hydrogenation and acidic sites. A co-solvent is necessary to mitigate furfural plugging during extended operation. Both ethanol and hydroxymethyl tetrahydrofuran are suitable co-solvents. Hydroxymethyl tetrahydrofuran is an intermediate in the reduction of furfural to alcohols and higher overall yields from furfural can be obtained by recycling unreacted hydroxymethyl tetrahydrofuran for use as the reaction solvent.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 15833-61-1, help many people in the next few years.Formula: C5H10O2

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

Synthetic Route of 15833-61-1, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol, molecular formula is C5H10O2. In a Patent£¬once mentioned of 15833-61-1

Heterocyclic compounds as inhibitors of rotomase enzymes

Compounds of the formula: wherein R1, Y, W, A and R2 are as defined above are inhibitors of rotamase enzymes in particular FKBP-12 and FKBP-52. The compounds therefore moderate neuronal regeneration and outgrowth and can be used for treating neurological disorders arising from neurodegenerative diseases and nerve damage.

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