18-Sep-21 News Some tips on 4249-72-3

The synthetic route of 4249-72-3 has been constantly updated, and we look forward to future research findings.

Adding a certain compound to certain chemical reactions, such as: 4249-72-3, 2-Phenoxy-1-phenylethanol, 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, Safety of 2-Phenoxy-1-phenylethanol, blongs to alcohols-buliding-blocks compound. Safety of 2-Phenoxy-1-phenylethanol

General procedure: In a typical reaction, 125 ML phosphate buffer (0.2 mol L-1, pH 7),90 ML distilled water, 265 ML AuNPs-GQDs18 (0.72 g L-1, 0.01 mg gold)were mixed. Then, 0.1 mg substrate in 50 ML ethanol was dried at 50 Cin an open bottle. The bottle was sealed after the AuNPs-GQDs18 solutionand 20 ML fresh H2O2 (30 g L-1) was injected into it. The reactionmixture was heated at 75 C for 4 h in a horizonal oscillator. The conversionand yield were determined by HPLC. The catalyst could be recoveredby dialysis (8000-140,000 Da) and reused for 2 times (seeTable S3).

The synthetic route of 4249-72-3 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Zhang, Fangwei; Zhang, Jiali; Guo, Shouwu; Inorganic Chemistry Communications; vol. 104; (2019); p. 105 – 109;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts