Category: 121-00-6

He, Zhen published the artcileSulfoxide-mediated oxidative cross-coupling of phenols, Quality Control of 121-00-6, the main research area is phenol nucleophile sulfoxide mediator oxidative cross coupling regioselective; arylphenol preparation; benzofuran preparation; hydroxy teraryl preparation.

A metal-free, oxidative coupling of phenols with various nucleophiles, including arenes, 1,3-diketones and other phenols was reported. Cross-coupling was mediated by a sulfoxide which inverts the reactivity of the phenol partner. Crucially, the process showed high selectivity for cross-vs. homo-coupling and allowed efficient access to a variety of aromatic scaffolds including biaryls, benzofurans and through an iterative procedure aromatic oligomers.

Chemical Science published new progress about Benzofurans Role: PRP (Properties), SPN (Synthetic Preparation), PREP (Preparation). 121-00-6 belongs to class ethers-buliding-blocks, name is 4-Hydroxy-3-tert-butylanisole, and the molecular formula is C11H16O2, Quality Control of 121-00-6.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Zhang, Junhui published the artcileComparative (co-)pyrolytic performances and by-products of textile dyeing sludge and cattle manure: Deeper insights from Py-GC/MS, TG-FTIR, 2D-COS and PCA analyses, Category: ethers-buliding-blocks, the main research area is kinetic copyrolysis gas char textile dyeing sludge cattle manure; Cattle manure; Char functional groups; Gaseous products; Kinetics; Textile dyeing sludge.

Not only does pyrolysis recover energy and value-added byproducts but also reduces waste stream volume The low volatiles and high ash contents of textile dyeing sludge (TDS) limit its mono-pyrolysis performance. This study aimed to conduct an in-depth anal. of its co-pyrolytic performance with cattle manure (CM). The co-pyrolysis enhanced the volatiles emission from the early devolatilization stage whose reaction mechanism shifted from a diffusion model to a reaction-order model. The further cracking of macromol. materials was mainly elucidated by the reaction-order model. The temperature dependency of the co-pyrolytic gases was of the following order: aliphatic hydrocarbons > CO2 > alcs., phenols, ethers, aldehydes, ketones, and carboxylic acids. The main co-pyrolytic volatile products were coumaran and 4-vinylguaiacol. The relative content of guaiacol-type components could be enhanced by co-pyrolysis and lowering the operational temperature to 450°C. The interaction of co-pyrolysis enriched the char aromaticity. Our findings provide practical insights into the control and application opportunities and limitations on the high value-added energy and products from the co-pyrolysis of TDS and CM.

Journal of Hazardous Materials published new progress about Alcohols Role: FMU (Formation, Unclassified), PEP (Physical, Engineering or Chemical Process), FORM (Formation, Nonpreparative), PROC (Process). 121-00-6 belongs to class ethers-buliding-blocks, name is 4-Hydroxy-3-tert-butylanisole, and the molecular formula is C11H16O2, Category: ethers-buliding-blocks.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem