Category: 24484-93-3

Electric Literature of 24484-93-3, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, 24484-93-3, Name is Methyl 4-chloropicolinate, SMILES is COC(=O)C1=NC=CC(Cl)=C1, belongs to pyridine-derivatives compound. In a article, author is Belusso, Anne C., introduce new discover of the category.

Vapor-liquid equilibrium pressure of ethanolamine hydrochloride, and vapor-solid equilibrium pressure of methylamine, pyridine, and trimethylamine hydrochlorides by thermogravimetric method

In this work, vapor-liquid and vapor-solid equilibrium pressure and enthalpies of amine hydrochlorides were determined using a thermogravimetric method. Ferrocene was used as the reference compound to determine the calibration constant k. Then, ammonium bromide, ammonium chloride and benzoic acid were used for testing the k-ferrocene. Experimental vapor-solid equilibrium pressure of methylamine hydrochloride obtained in this study showed good agreement with recent literature data. For the other substances investigated, ethanolamine hydrochloride, pyridine hydrochloride, and trimethylamine hydrochloride, no reliable equilibrium data is available in the open literature. Among these substances, ethanolamine hydrochloride was found to be the less volatile, followed by methylamine, trimethylamine, and pyridine hydrochloride. Regarding the equilibrium enthalpies found in this work, all salts have shown a similar value. This can be explained by the similar reaction (dissociation) that takes place for these substances.

Electric Literature of 24484-93-3, 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 24484-93-3 is helpful to your research.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – 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. 24484-93-3, Name is Methyl 4-chloropicolinate, molecular formula is C7H6ClNO2. In an article, author is Staszak, Katarzyna,once mentioned of 24484-93-3, Formula: C7H6ClNO2.

Surface activity measurements and quantum molecular modeling – The way to extraction behavior knowledge?

The interfacial behavior of novelty hydrophobic carboximidamide derivatives extractants has been presented. The influence of the type of alkyl groups and their position in the pyridine ring, as well as the type of solvent, on the adsorption and metal extraction has been investigated. Moreover, the relationship between the interfacial activity and the dependence of the extraction efficiency has been discussed. The interfacial behavior of the extractants has been also confirmed by quantum molecular modeling. It has been confirmed that knowledge of extraction phenomena such as extractants adsorption on the liquid/liquid interface as well as knowledge of the structure of the molecules allows for an initial assessment of the extraction properties of the extractants. (C) 2020 Elsevier B.V. All rights reserved.

Interested yet? Keep reading other articles of 24484-93-3, you can contact me at any time and look forward to more communication. Formula: C7H6ClNO2.

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

Application of 24484-93-3, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 24484-93-3, name is Methyl 4-chloropicolinate. This compound has unique chemical properties. The synthetic route is as follows.

4-Chloro-2-picolinic acid methyl ester(10 g, 58.3 mmol) was added to 70 mL of methanol and stirred to dissolve,Cooled to 0-5 C with stirring,Then, methylamine (5.4 g, 0.175 mol) in methanol (40 mL) was added dropwise with constant stirring,The dropping process temperature is maintained at 0-5 C.Drop finished,Reaction at 0-5 C for 4 h.The solvent is recovered under reduced pressure,The residue was added to 200 mL of ethyl acetate,Stir evenly after filtration,The filtrate was washed with saturated brine,Dried over anhydrous sodium sulfate,Concentrated under reduced pressure,crystallization,filter,washing,dry,To give 9.4 g of pale yellow crystals,Yield 94.5%

According to the analysis of related databases, 24484-93-3, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Yantai University; Yao Jianwen; Kong Xiangkai; Chen Jing; Wang Chengpeng; Zhang Guoying; (26 pag.)CN104045598; (2017); B;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem