Product Details of 150-19-6. Recently I am researching about RADICAL-MOLECULE REACTIONS; TRANSITION-STATE MODEL; THERMAL-DECOMPOSITION; LIGNOCELLULOSIC BIOMASS; ANISOLE PYROLYSIS; FLAME STRUCTURE; RATE CONSTANTS; KINETICS; OH; MECHANISM, Saw an article supported by the Fundamental Research Funds for the Central Universities of ChinaFundamental Research Funds for the Central Universities [2020ZDPYMS05]; Shanxi Scholarship Council of China [2020-115]. Published in ELSEVIER in AMSTERDAM ,Authors: Wang, QD; Sun, MM; Liang, JH. The CAS is 150-19-6. Through research, I have a further understanding and discovery of m-Methoxyphenol
The growing interest in the use of bio-oils requires a detailed understanding of its combustion chemical kinetics. Bio-oils contain a large variety of oxygenated organic species, in which substituted phenolic compounds are among the most significant fractions. Hence, accurate assessment of key reaction rate constants and systematically investigated the structural effect on the reactivity are critical. This work reports a systematic theoretical study of the hydrogen abstraction reactions from phenol, anisole, o-guaiacol, m-guaiacol, and p-guaiacol, which are considered as reference components in bio-oil surrogates. The hydrogen abstraction reactions by five different radicals (H/CH3/O(P-3)/OH/HO2) are investigated at ROCBS-QB3//M06-2X/cc-pVTZ level. The highpressure limit rate constants are computed via transition state theory with Eckart tunnelling and the 1-D hindered rotor approximation. Comparisons of site-specific hydrogen abstractions from the studied species with other related species are performed to understand the effects of the aromatic ring and side-chain substituent on hydrogen abstractions.
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Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles