170112-66-0

Basic information

• Product Name: 3,4,5-TRIFLUOROIODOBENZENE
• Synonyms: 3,4,5-TRIFLUOROIODOBENZENE;1,2,3-trifluoro-5-iodobenzene;5-Iodo-1,2,3-trifluorobenzene;1-Iodo-3,4,5-Trifluorobenzene
• CAS NO: 170112-66-0
• Molecular Formula: C₆H₂F₃I
• Molecular Weight: 257.98
• Mol File: 170112-66-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 176.4 °C at 760 mmHg
• Flash Point: 65.1 °C
• Appearance: /
• Density: 2.078 g/cm³
• Vapor Pressure: 1.47mmHg at 25°C
• Refractive Index: 1.543
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 3,4,5-TRIFLUOROIODOBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,5-TRIFLUOROIODOBENZENE(170112-66-0)
• EPA Substance Registry System: 3,4,5-TRIFLUOROIODOBENZENE(170112-66-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• HazardClass: IRRITANT
• Hazardous Substances Data: 170112-66-0(Hazardous Substances Data)

Usage

General Description

3,4,5-Trifluoroiodobenzene is a chemical compound with the formula C6H2F3I. It is a colorless liquid at room temperature and is commonly used as a reagent in organic synthesis. The trifluoro group on the benzene ring makes the compound more reactive and helps in various chemical reactions. 3,4,5-Trifluoroiodobenzene is also used as a building block in the production of pharmaceuticals and agrochemicals, due to its ability to introduce the trifluoromethyl group to organic molecules. It is considered to be an important intermediate compound in the field of organic chemistry and plays a significant role in the development of new materials and pharmaceuticals.

InChI:InChI=1/C6H2F3I/c7-4-1-3(10)2-5(8)6(4)9/h1-2H

Upstream product

• 138526-69-9 3,4,5-trifluoro-1-bromobenzene 

Downstream Products

• 205526-31-4 (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(3,4,5-trifluorophenyl)propanoic acid 
• 505058-38-8 3,3′,4,4′,5,5′-hexafluoro-1,1′-biphenyl 
• 137019-95-5 3,4,5-trifluoro-4'-(4-pentyl-cyclohexyl)-biphenyl 

Relevant articles and documents

BIS(3-PHENETHYLOXYPHENYL) DISULFIDE AND METHOD FOR PRODUCING THE SAME

PROBLEM TO BE SOLVED: To provide a disulfide derivative that is an intermediate allowing a substituted phenyl ether compound having pest controlling effect to be synthesized conveniently and efficiently and a method for producing the same. SOLUTION: The present invention provides a bis(3-phenethyloxyphenyl) disulfide derivative represented by formula (1) (X is H or a halogen atom; R1 and R2 are a halogen atom, or R1 and R2 together bond to one O or S to represent (=O) or (=S); Y1-Y3 are a halogen atom or a C1-4 haloalkyl group). SELECTED DRAWING: None COPYRIGHT: (C)2016,JPO&INPIT

METHOD FOR PRODUCING SUBSTITUTED PHENYL ETHER COMPOUND

PROBLEM TO BE SOLVED: To provide a method for producing conveniently and efficiently a substituted phenyl ether compound having pest controlling effect. SOLUTION: The present invention provides a method for producing a substituted phenyl ether derivative in which a substituted phenyl ether derivative represented by formula (1) reacts with an oxidizing agent for sulfoxidation of sulfide, and also provide a method for producing a compound represented by formula (1) (X is H or a halogen atom; R1 and R2 are a halogen atom; Y1-Y3 are a halogen atom or a C1-C4 haloalkyl group). SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Method for producing tetrakis ( fluoroaryl) borate-magnesium compound

Fluoroaryl magnesium halide is reacted with a boron compound so that a molar ratio of the fluoroaryl magnesium halide to the boron compound is not less than 3.0 and not more than 3.7, so as to produce a tetrakis (fluoroaryl) borate·magnesium compound. With this method, there occurs no hydrogen fluoride which corrodes a producing apparatus and requires troublesome waste water treatment.