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

Uses

Used in Organic Synthesis:
3,4,5-Trifluoroiodobenzene is used as a reagent in organic synthesis for its increased reactivity due to the trifluoro group. This property aids in various chemical reactions, facilitating the formation of desired products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3,4,5-Trifluoroiodobenzene is utilized as a building block. Its ability to introduce the trifluoromethyl group to organic molecules makes it a valuable component in the synthesis of new pharmaceuticals, contributing to the development of innovative treatments and medications.
Used in Agrochemical Production:
3,4,5-Trifluoroiodobenzene also finds application in the agrochemical sector, where it serves as a key intermediate in the synthesis of various agrochemicals. Its role in creating compounds with the trifluoromethyl group is essential for enhancing the effectiveness of these products in agricultural applications.
Overall, 3,4,5-Trifluoroiodobenzene is a multifaceted compound with applications spanning across different industries, primarily due to its unique structural features and reactivity.

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 
• 1616828-85-3 6-(3,4,5-trifluorophenyl)-8-((2-(trimethylsilyl)ethoxy)methoxy)-3-((2-(trimethylsilyl)ethoxy)methyl)quinazolin-4(3H)-one 
• 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

The method for manufacturing the same and hydroxybenzenesulfonic deriv. phenethyloxy substd. (by machine translation)

PROBLEM TO BE SOLVED: having a harmful effect substd. rnethylphenylsilicone compd. hydroxybenzenesulfonic deriv. synthesizable substd. phenethyloxy easily and efficiently and to provide a manufacturing method thereof. SOLUTION: phenethyloxy substd. represented by hydroxybenzenesulfonic deriv. eq. (1). (= O or = S; Y 1-Y 3 is H, Br, mercapto group, amino group, nitro group, or thiocyanate group; X is H or a halogen atom; R 1 and R 2 the A is a halogen atom or the alkyl group or a halogen atom halopyridine C 1-C 4 of) selected drawing: no (by machine translation)

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

DIFLUOROALKYLBENZENE DERIVATIVE AND METHOD FOR PRODUCING THE SAME

PROBLEM TO BE SOLVED: To provide a difluoroalkylbenzene 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 method for producing a 2-substituted phenyl-2,2-difluoro ethanol derivative by allowing a 2-substituted phenyl-2,2-difluoroacetate derivative represented by formula (1c) to be prepared by the following reaction and further making the derivative react with a reductant such as hydrogenated boron sodium (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.

Synthesis and mesomorphic properties of some liquid crystals with 2,3,5,6-tetrafluorophenylene unit

Nine fluorosubstituted liquid crystals have been synthesized and their mesomorphic properties have been studied by texture observation in a polarizing microscope and confirmed by DSC. They show enantiotropic smectic A and nematic phases. The effect of ter