Category: 33332-25-1

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. 33332-25-1, Name is Methyl 5-chloropyrazine-2-carboxylate, molecular formula is , belongs to Pyrazines compound. In a document, author is Dehury, Niranjan, HPLC of Formula: C6H5ClN2O2.

Tandem alpha/beta-alkylation and transfer hydrogenation by heterodimetallic ruthenium-iridium complex

Herein, we present a new and air-stable polypyridyl based heterodimetallic complex [cp*Ir-III(mu-L)Ru-II(p-cym)] (PF6)(2) (5) exhibiting facile tandem alpha/beta-alkylation/transfer hydrogenation of ketones/alcohol under mild re-action conditions. The heterodimetallic 5 is found to show better reactivity and selectivity as compared to their homodimetallic analogues (3 and 4), monometallic (1 and 2) and dimeric precursors [cp*IrCl(mu-Cl)](2) and [(p-cym)RuCl(mu-Cl)](2). In addition, the present catalytic system 5 demonstrates a good flexibility and selective formation of alpha-alkylated ketones (C) or beta-alkylated alcohol (D) by simple variation of reagents and reaction condition which may be envisioned to play a pivotal role in organic and organometallic chemistry as it lead to the development of pharmaceutically relevant intermediates for the synthesis of different types of heterocycles.

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 33332-25-1, in my other articles. HPLC of Formula: C6H5ClN2O2.

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. In an article, author is Takabatake, Tohru, once mentioned the application of 33332-25-1, Name is Methyl 5-chloropyrazine-2-carboxylate, molecular formula is C6H5ClN2O2, molecular weight is 172.57, MDL number is MFCD01632102, category is Pyrazines. Now introduce a scientific discovery about this category, Recommanded Product: Methyl 5-chloropyrazine-2-carboxylate.

Chemical and Biochemical Reactions of Aromatic Furazan Compounds

Aromatic furazan has numerous pharmacologic and industrial applications. As part of our work on aromatic furazan chemistry and biochemistry, benzofurazan N-oxides, on irradiation using a high-pressure mercury lamp with a Pyrex filter in acetonitrile containing a little water, afforded 1H-azepine-2,7-dione. Mechanistic studies on the photoreaction using a low-pressure mercury lamp and photosensitizer suggest that photosensitized formation of 1H-azepine-2,7-dione with the aromatic hydrocarbon may be carried out by reabsorption of fluorescence. Quinoxaline 1,4-dioxide, phenazine 5,10-dioxide, and pyrido [2,3-b] pyrazine derivatives were synthesized from the corresponding aromatic or heteroaromatic furazan N-oxides by silica gel or molecular sieves under solvent-free conditions using microwave irradiation. The toxicities of some benzofurazans were examined on Escherichia coli; these may due to their reduction within the E. coli cell and their reoxidization by molecular dioxygen to form superoxide and hydrogen peroxide. The formation of 4,7-dicyanobenzofurazan anion radical in the E. coli cell suspension-4,7-dicyanobenzofurazan-glucose system in the absence of O-2 was followed by ESR spectroscopy. 4,7-Dimethylbenzofurazan was transformed by O-1(2) produced by irradiation of C-60 into 4,7-dimethylbenzofurazan 4,7-endoperoxide. The endoperoxide decomposed back to 4,7-dimethylbenzofurazan at room temperature. 4,7-Dimethylbenzofurazan was transformed by irradiation with the third harmonic of a Quanta-Ray Nd:YAG laser (355 nm) into (2Z,4Z)-2,5-dimethylhexa-2,4-dienedinitrile monoxide. Irradiation of 4,7-dimethylbenzofurazan yielded a photoproduct with a quantum yield 0.48 and chemical yield 99%.

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 33332-25-1, Recommanded Product: Methyl 5-chloropyrazine-2-carboxylate.

Reference of 33332-25-1, 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. 33332-25-1, Name is Methyl 5-chloropyrazine-2-carboxylate, SMILES is ClC1=CN=C(C=N1)C(=O)OC, belongs to Pyrazines compound. In a article, author is Benecke, Jannik, introduce new discover of the category.

A Flexible and Porous Ferrocene-Based Gallium MOF with MIL-53 Architecture

A new gallium based metal-organic framework, denoted as Ga-MIL-53-FcDC, with the chemical formula [Ga(OH)(FeC12H8O4)] was synthesized using the ferrocene containing linker molecule 1,1′-ferrocenedicarboxylic acid (H(2)FcDC, FeC12H10O4). The porous nature of the compound could be confirmed by nitrogen sorption and a specific surface area of 270 m(2)/g was determined. The persistence of the ferrocene complex inside the structure was confirmed by Mossbauer-, EPR and UV/VIS-spectroscopy. Ga-MIL-53-FcDC shows structural flexibility depending on which guest molecule is located in the pores of the compound. The mechanism of structural flexibility was analyzed by means of powder X-ray diffraction adsorbing pyrazine or iodine. The flexibility of the crystal structure can be attributed to the torsion of the GaO6 octahedra in the IBU respective to each other and the torsion of the carboxylate groups of FcDC(2-) relative to the aromatic ring.

Reference of 33332-25-1, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 33332-25-1 is helpful to your research.

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 33332-25-1, Name is Methyl 5-chloropyrazine-2-carboxylate, SMILES is ClC1=CN=C(C=N1)C(=O)OC, in an article , author is Sorkhi, Seyyed Erfan Sadati, once mentioned of 33332-25-1, Computed Properties of C6H5ClN2O2.

Introduction of a novel dicationic Bronsted acidic ionic liquid based on pyrazine and its application in the synthesis of xanthenediones and 3, 4-dihydropyrimidin-2(1H)-ones under solvent-free conditions

A novel dicationic Bronsted acidic ionic liquid based on pyrazine has been prepared and characterized by FTIR, H-1 NMR, C-13 NMR, MS, thermal gravimetric and differential thermal gravimetric analysis and also Hammett acidity function. The prepared dicationic ionic liquid is found to be an efficient and reusable catalyst for the synthesis of xanthenediones and 3,4-dihydropyrimidin-2(1H)-ones under solvent-free conditions. The merits of the developed procedure include novelty in terms of the ionic liquid, easy preparation of the ionic liquid, easy workup, reusability of the catalyst, high yield, short reaction time and absence of toxic organic solvent.

Interested yet? Read on for other articles about 33332-25-1, you can contact me at any time and look forward to more communication. Computed Properties of C6H5ClN2O2.

Related Products of 33332-25-1, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 33332-25-1, Name is Methyl 5-chloropyrazine-2-carboxylate, SMILES is ClC1=CN=C(C=N1)C(=O)OC, belongs to Pyrazines compound. In a article, author is Chen, Yuyu, introduce new discover of the category.

Changes in volatile compounds of fermented minced pepper during natural and inoculated fermentation process based on headspace-gas chromatography-ion mobility spectrometry

Changes in volatile compounds of fermented minced pepper (FMP) during natural fermentation (NF) and inoculated fermentation (IF) process were analyzed by the headspace-gas chromatography-ion mobility spectrometry (HS-GC-IMS). A total of 53 volatile compounds were identified, including 12 esters, 17 aldehydes, 13 alcohols, four ketones, three furans, two acids, one pyrazine, and one ether. Generally, fermentation time played an important role in volatile compounds of FMP. It was found that most esters, aldehydes, and alcohols obviously decreased with the increase in fermentation time, including isoamyl hexanoate, methyl octanoate, gamma-butyrolactone, phenylacetaldehyde, methional, and E-2-hexenol. Only a few volatile compounds increased, especially for 2-methylbutanoic acid, 2-methylpropionic acid, linalool, ethanol, and ethyl acetate. However, no significant difference in volatile compounds was found between NF and IF samples at the same fermentation time. In addition, the fermentation process in all samples was well discriminated as three stages (0 days; 6 day; and 12, 18, and 24 days), and all volatile compounds were divided into two categories (increase and decrease) based on principal component analysis and heat map.

Related Products of 33332-25-1, 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 33332-25-1.

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, Recommanded Product: Methyl 5-chloropyrazine-2-carboxylate33332-25-1, Name is Methyl 5-chloropyrazine-2-carboxylate, SMILES is ClC1=CN=C(C=N1)C(=O)OC, belongs to Pyrazines compound. In a article, author is Tantawy, Eman S., introduce new discover of the category.

Synthesis, characterization of some pyrazine derivatives as anti-cancer agents: In vitro and in Silico approaches

In continuation of our interest on the synthesis of fused quinoxalines and pyrazines derivatives and due to the resultant pharmacological interest in compounds which belong to these heterocyclic derivatives. In this manuscript, we direct for preparation of some indenoquinoxaline and pyrazine derivatives, with spectral characterization using different spectral techniques including IR, NMR, together with elemental analyses. The newly synthesized derivatives were subjected to cytotoxic screening using the MTT assay against MCF-7 and A549 cell lines. Compounds 6, 8a, 9, 10, and 11 exhibited a potent cytotoxic activity, especially compound 11 with IC50 values 5.4 and 4.3 mu M against MCF-7 and A549, respectively. Molecular docking calculations of the tested derivatives exhibited a good binding affinity towards EGFR receptor binding site, which might explain their proposed mode of action. (C) 2020 Elsevier B.V. All rights reserved.

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. you can also check out more blogs about 33332-25-1. Recommanded Product: Methyl 5-chloropyrazine-2-carboxylate.

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 33332-25-1, Name is Methyl 5-chloropyrazine-2-carboxylate, SMILES is ClC1=CN=C(C=N1)C(=O)OC, in an article , author is Al-Turk, Anhar, once mentioned of 33332-25-1, Recommanded Product: Methyl 5-chloropyrazine-2-carboxylate.

Isolation and Molecular Characterization of Antibiotic Producing Bacillus licheniformis Strains Isolated from Soil

Currently, there is an increase prevalence of antibiotic-resistant bacteria worldwide. Therefore, the need for characterization of naturally occuring antibiotics with less antibiotic resistance is required. Soil resources contains valuable antibiotic producing microorganisms that increasingly being utilized for the production of suitable antibiotics. Therefore, this study aimed at identifying an antibiotic bacteria with ability of producing antibiotic that is isolated from soil samples collected from Al Zarqa provenance, an arid area in Jordan. Morphological and biochemical characterization of the isolates were carried out and found that all of the isolates belong to Bacillus genus. Further confirmation of the characterization of the bacteria was done by ribosomal RNA and PCR. The results reveal that the isolates represent Basilluslicheniformis. These bacilli were further investigated for antimicrobial activities against 6 ATCC human pathogens viz., S. aureus, S. pneumonia, Salmonella typhi., E. coli, P. mirabels and E. cloacae. Additionally, the results of Gas Chromatography Mass Spectrometry (GCMS) of ethyl acetate extracts for B. licheniformis secondary metabolites showed that they contain two main antimicrobial compounds namely Pyrrolo [1, 2-a] pyrazine-1, 4-dione,hexahydro and Trans-13-octadecenoic acid. The present work maybe suggests that soil isolates from the studied arid area include antibiotic producing strains that can be utilized commercially.

Interested yet? Read on for other articles about 33332-25-1, you can contact me at any time and look forward to more communication. Recommanded Product: Methyl 5-chloropyrazine-2-carboxylate.

Reference of 33332-25-1, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 33332-25-1, Name is Methyl 5-chloropyrazine-2-carboxylate, SMILES is ClC1=CN=C(C=N1)C(=O)OC, belongs to Pyrazines compound. In a article, author is Shivanna, Mohana, introduce new discover of the category.

Control of local flexibility towardsp-xylene sieving in Hofmann-type porous coordination polymers

Adsorption-based xylene isomer separation is more energy efficient than conventional processes. Herein, three isostructural Hofmann-type porous coordination polymers (PCPs), {M(Pz)[Ni(CN)(4)](n)} (M = Fe, FePzNi, Co, CoPzNi, and Ni, NiPzNi; Pz = pyrazine) were synthesized and shown to exhibit coordination-dependent lability for the selectivity towardp-xylene overm- ando-xylene.

Reference of 33332-25-1, 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 33332-25-1.

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 33332-25-1, name is Methyl 5-chloropyrazine-2-carboxylate, A new synthetic method of this compound is introduced below., Computed Properties of C6H5ClN2O2

Diisobutylaluminum hydride (4.29 mL, 4.29 mmol) was added dropwise over 5 min to a solution of methyl 5-chloropyrazine-2-carboxylate (185 mg, 1.07 mmol) in tetrahydrofuran (10 mL) at -70 0C under an athmosphere of nitrogen. The reaction mixture was stirred at – 70 0C for 5 min and then allowed to reach ambient temperature and stirred over night. The reaction mixture was cooled on ice and approximately 2 mL of 1 M sodium hydroxide was added dropwise while stirring. The reaction mixuture was diluted with diethyl ether and stirred for 45 min at ambient temperature and then filtered. The filtrate was concentrated in vacuo and the residue was purified by column chromatography using a gradient of ethyl acetate in heptane to yield 43 mg (28 %) of the title product; 1H NMR (400 MHz, DMSO- dbeta) delta ppm 8.72 (d, 1 H), 8.52 – 8.55 (m, 1 H), 5.71 (t, 1 H), 4.64 (d, 2 H);

The synthetic route of 33332-25-1 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; ASTRAZENECA AB; WO2008/130320; (2008); A2;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

Synthetic Route of 33332-25-1, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 33332-25-1, name is Methyl 5-chloropyrazine-2-carboxylate, This compound has unique chemical properties. The synthetic route is as follows.

Example 29 5- [2 (R)- (3-CHLORO-4-METHANESULFONYL-PHENYL)-3-CYCLOPENTYL-PROPIONYLAMINO]- PYRAZINE-2-CARBOXYLIC acid HYDROXYAMIDE [000197] A solution of methyl 5-chloropyrazine-2-carboxylate (30.00 g, 0.17 mol) in tetrahydrofuran (87 mL) was treated with a solution of potassium carbonate (72.08 g, 0.52 mol) in water (261 mL). The resulting reaction mixture stirred at 25C for 42 h. The reaction mixture was then acidified to a pH of about 2 with concentrated hydrochloric acid, diluted with a saturated aqueous sodium chloride solution (300 mL), and was continuously extracted with ethyl acetate (4L total) until no product was present in the aqueous layer. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to afford 5-chloro-pyrazine-2-carboxylic acid (26.54 g, 96%) as an off-white solid: mp 150-151C ; EI-HRMS m/e calcd for CSH3CIN202 (M 157.9883, found 157.9877.

The chemical industry reduces the impact on the environment during synthesis Methyl 5-chloropyrazine-2-carboxylate. I believe this compound will play a more active role in future production and life.

Reference:
Patent; F. HOFFMANN-LA ROCHE AG; WO2004/52869; (2004); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem