29052-00-4

Basic information

• Product Name: 3-IODOPHENETOLE
• Synonyms: 1-ethoxy-3-iodobenzene;3-Iodophenylethyl ether;m-Iodophenetole;3-IODOPHENETOLE
• CAS NO: 29052-00-4
• Molecular Formula: C₈H₉IO
• Molecular Weight: 248.06
• Product Categories: Anisoles, Alkyloxy Compounds & Phenylacetates;Iodine Compounds
• Mol File: 29052-00-4.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-IODOPHENETOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-IODOPHENETOLE(29052-00-4)
• EPA Substance Registry System: 3-IODOPHENETOLE(29052-00-4)

Safety Data

• Hazardous Substances Data: 29052-00-4(Hazardous Substances Data)

Usage

General Description

3-Iodophenetole is a chemical compound with the molecular formula C8H9IO. It is a halogenated phenetole, which is an aromatic ether. 3-Iodophenetole is used in organic synthesis as a versatile reagent for the introduction of the iodophenyl group into various organic compounds. It can also be used as a building block in the preparation of pharmaceuticals and other biologically active molecules. 3-Iodophenetole has a wide range of applications in the field of medicinal chemistry and is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also a useful tool in the study of organic reactions and mechanisms, 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 articles and documents

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.