Category: 5223-06-3

Reference of 5223-06-3, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 5223-06-3, Name is 2-(5-Ethylpyridin-2-yl)ethanol, SMILES is CCC1=CN=C(CCO)C=C1, belongs to pyridine-derivatives compound. In a article, author is Karupnaswamy, Ramesh, introduce new discover of the category.

The First Fused N-Heterocyclic Imidazole Pyridine Selones and Their Coordination Ability Towards Bismuth(III) Salts

The first fused N-heterocyclic selone ligands, namely 2-(2′,6′-diisopropylphenyl) imidazole[1,5-a] pyridine-2-selone and 2-(2,4,6-trimethylphenyl) imidazole[1,5-a]pyridine-2-selone were isolated and their coordination ability was explored with bismuth trihalides to isolate the steric controlled bismuth(III) di-nuclear complexes. Notably, a similar approach with N,N’-disubstituted imidazole selone, such as imidazole-1-methyl-3-(2-iso-propyl)selone, gave the first polynuclear bismuth(III) selone chain. These new bismuth(III) selones were characterized by elemental analysis, FT-IR, multinuclear (H-1 and C-13) NMR spectroscopy, and single-crystal X-ray diffraction techniques. In solid-state structure, these new bismuth(III) selone complexes depict the unique coordination environment, geometry, and bonding features.

Reference of 5223-06-3, 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 5223-06-3 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. 5223-06-3, Name is 2-(5-Ethylpyridin-2-yl)ethanol, SMILES is CCC1=CN=C(CCO)C=C1, in an article , author is Yogita, once mentioned of 5223-06-3, Recommanded Product: 2-(5-Ethylpyridin-2-yl)ethanol.

The selective conversion of furfuryl alcohol to ethyl levulinate over Zr-modified tungstophosphoric acid supported on beta-zeolites

Catalysts of zirconium-exchanged proton-containing tungstophosphoric acid (TPA) supported on beta-zeolites were prepared by an impregnation method for the selective alcoholysis of furfuryl alcohol into ethyl levulinate. The prepared catalysts were characterized by different spectroscopic techniques. The results indicated the existence of a Keggin ion structure of TPA after its modification with Zr ions and successive dispersion on beta-zeolites. The introduction of Zr in TPA generated Lewis acidic sites in the catalyst. Pyridine-adsorbed FT-IR confirmed the presence of both Bronsted and Lewis acidic sites in catalysts. The catalytic activity for the alcoholysis of furfuryl alcohol depends on the strength of both Bronsted and Lewis acids of the catalyst. Among these catalysts, 20%Zr(0.75)TPA/beta-zeolite was active for the alcoholysis of furfuryl alcohol with a 96% yield of ethyl levulinate. Optimal conditions were established to obtain maximum yield. A plausible reaction mechanism was also proposed. The catalyst was reused without any appreciable loss of activity.

Interested yet? Read on for other articles about 5223-06-3, you can contact me at any time and look forward to more communication. Recommanded Product: 2-(5-Ethylpyridin-2-yl)ethanol.

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

Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. , HPLC of Formula: C9H13NO, 5223-06-3, Name is 2-(5-Ethylpyridin-2-yl)ethanol, molecular formula is C9H13NO, belongs to pyridine-derivatives compound. In a document, author is Spiewak, Amanda M., introduce the new discover.

Ruthenium-Catalyzed C-H Arylation of 1-Naphthol with Aryl and Heteroaryl Halides

While 8-aryl-1-napthols are promising dye molecules and useful intermediates in the synthesis of polycyclic aromatic hydrocarbons, they can be difficult to access. A new, rutheniumcatalyzed method for peri-C-H arylation of 1-naphthol with a variety of aryl and heteroaryl halides (iodides, bromides) is reported that overcomes the limitations of previous palladium-catalyzed approaches. Yields for the 21 examples range from 16 to 99%, with an average of 71%, and the reaction tolerates a variety of functional groups: pyridine, pyrimidine, primary aniline, aldehyde, and ester.

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 5223-06-3. HPLC of Formula: C9H13NO.

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

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels. 5223-06-3, Name is 2-(5-Ethylpyridin-2-yl)ethanol, molecular formula is C9H13NO. In an article, author is Hamza, Eman Kh,once mentioned of 5223-06-3, Product Details of 5223-06-3.

Synthesis and in vitro evaluation of novel tetralin-pyrazolo[3,4-b]pyridine hybrids as potential anticancer agents

New hybrids of tetralin-pyrazolo[3,4-b]pyridine were synthesized in good yields. The structures of newly synthesized compounds were confirmed by IR, NMR, MS, and elemental analyses. Some of the new compounds were in vitro evaluated as antiproliferative candidates against two human cancer cell lines (HCT116 and MCF-7). Most of the examined derivatives showed promising anticancer activity.

Interested yet? Keep reading other articles of 5223-06-3, you can contact me at any time and look forward to more communication. Product Details of 5223-06-3.

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

5223-06-3, Adding some certain compound to certain chemical reactions, such as: 5223-06-3, name is 2-(5-Ethylpyridin-2-yl)ethanol,molecular formula is C9H13NO, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 5223-06-3.

General procedure: To a solution of A1B1 (1.0mmol) and triphenylphosphine (1.5mmol) in anhydrous tetrahydrofuran (3mL), added C1 or C2 (2.0mmol) and dropwise added diethyl azodicarboxylate (DEAD, 1.5mmol) in anhydrous and anoxybiotic conditions. The reaction mixture was stirred at-2C for 30min, and then stirred at room temperature for 24h. After completion of reaction was monitored through TLC, the reaction mixture was filtered and washed with ether and saturated salt water to get products because there would be a solid precipitate.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of 5223-06-3.

Reference:
Article; Wang, Fang; Sun, Jun-Rong; Huang, Mei-Yan; Wang, Hui-Ying; Sun, Ping-Hua; Lin, Jing; Chen, Wei-Min; European Journal of Medicinal Chemistry; vol. 72; (2014); p. 35 – 45;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem