29052-00-4

Usage

Uses

Used in Organic Synthesis:
3-Iodophenetole is used as a reagent for the introduction of the iodophenyl group into various organic compounds. Its ability to be easily incorporated into different molecules makes it a valuable tool in organic synthesis.
Used in Pharmaceutical Preparation:
3-Iodophenetole serves as a building block in the preparation of pharmaceuticals and other biologically active molecules. Its presence in the synthesis process contributes to the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-Iodophenetole has a wide range of applications. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, playing a crucial role in the creation of new and effective compounds.
Used in Organic Reactions and Mechanisms Study:
3-Iodophenetole is also a useful tool in studying organic reactions and mechanisms. Its unique properties allow researchers to gain insights into the behavior of different chemical reactions, making it a valuable compound in the field of organic chemistry.

Upstream product

• 74-96-4 ethyl bromide 
• 626-02-8 3-Iodophenol 

Downstream Products

• 86704-82-7 3-ethoxybenzenethiol 

Relevant academic research and scientific papers

Discotic liquid crystals of transition metal complexes, 53?: Synthesis and mesomorphism of phthalocyanines substituted by m -alkoxyphenylthio groups

We have successfully synthesized a series of novel octakis(m-alkoxyphenylthio)phthalocyaninato copper(II) complexes, (m-CnOPhS)8PcCu (n = 2, 4, 6, 8, 10, 12, 14, 16: 1b～1i), by our developed method to reveal their mesomorphism. The phase transition behavior and mesophase structures have been established by using a polarizing optical microscope, a differential scanning calorimeter, and a temperature-dependent small angle X-ray diffractometer. Interestingly, the very short chain-substituted derivatives, (m-C1OPhS)8PcCu (1a) and (m-C2OPhS)8PCu (1b), show a hexagonal ordered columnar (Colho) mesophase, whereas each of the other longer-chain-substituted derivatives, (m-CnOPhS)8PcCu (n = 4～16: 1c～1i), shows only rectangular ordered columnar (Colro) mesophase(s). In contrast to the present longer-chain-substituted phenylthio derivatives, each of the previous longer-chain-substituted phenoxy derivatives, (m-CnOPhO)8PcCu (n = 10-20), shows a different columnar mesophase of Colho. We discuss this difference of mesomorphism from the viewpoint of the different steric hindrance originated by the peripheral substituents, PhO and PhS groups. Moreover, we could estimate the optical band gaps of (m-C10OPhO)8PcCu and (m-C10OPhS)8PcCu (1f) from absorption edge of the Q-bands to be 1.79 eV and 1.70 eV, respectively. Therefore, the phenylthio-substituted derivative gave a narrower band gap byca. 0.1 eV in comparison with the phenoxy-substituted derivative.