Synthesis and Biological Activity of N-Aroyl (Aryloxyacetyl)-N’-ferrocenyl Thiourea Derivatives was written by Zhang, Qiong;Zhao, Bihong;Song, Yangyang;Hua, Chengwen;Gou, Xiaofeng;Chen, Bang;Zhao, Junlong. And the article was included in Heteroatom Chemistry in 2015.Related Products of 1877-75-4 This article mentions the following:
In this study, the synthesis of aminoferrocene was improved and a series of novel ferrocene-containing thiourea compounds were designed and synthesized as potential plant growth regulators. All the new compounds were characterized by IR, 1H NMR, and x-ray crystallog. Furthermore, the cytokinin and auxin activities of 5c and 5a–i were investigated. Notably, compounds 5e, 5g, and 5j in a concentration of 50 μg/mL exhibited significant cytokinin activity, and compounds 5b and 5h in a concentration of 50 μg/mL exhibited higher auxin activity than indoleacetic acid. In the experiment, the researchers used many compounds, for example, 2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4Related Products of 1877-75-4).
2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4) belongs to ethers. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Related Products of 1877-75-4
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem