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2,4,6-Trifluoroiodobenzene, with the molecular formula C6H2F3I, is a chemical compound that serves as a crucial intermediate in organic synthesis. It is renowned for its unique properties, such as its versatility as a building block for synthesizing a range of fluorine-containing organic molecules. 2,4,6-TRIFLUOROIODOBENZENE's trifluoromethyl and iodo functional groups endow it with special characteristics that make it valuable for research in medicinal and material sciences, as well as for its applicability in various chemical reactions, including cross-coupling reactions.

506407-82-5

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506407-82-5 Usage

Uses

Used in Pharmaceutical Industry:
2,4,6-Trifluoroiodobenzene is used as a key intermediate for the synthesis of pharmaceutical compounds due to its ability to enhance the biological activity and pharmacokinetic properties of drug molecules. Its unique functional groups facilitate the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4,6-Trifluoroiodobenzene is utilized as a precursor in the production of various agrochemicals, contributing to the development of pesticides and herbicides with enhanced performance and selectivity for targeted pests and weeds.
Used in Organic Synthesis:
2,4,6-Trifluoroiodobenzene is employed as a versatile building block in organic synthesis for creating complex organic compounds. Its reactivity in cross-coupling reactions allows for the formation of diverse molecular structures, which are essential in the synthesis of specialty chemicals, materials, and other organic compounds.
Used in Medicinal Chemistry Research:
2,4,6-Trifluoroiodobenzene is used as a research compound in medicinal chemistry to explore its potential in the development of new therapeutic agents. Its unique properties and reactivity make it a valuable tool for studying structure-activity relationships and optimizing drug candidates.
Used in Material Science Research:
In material science, 2,4,6-Trifluoroiodobenzene is utilized for the synthesis of novel materials with specific properties, such as high thermal stability, chemical resistance, or unique electronic characteristics. Its functional groups can be tailored to create materials with tailored properties for various applications, including sensors, electronic devices, or advanced coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 506407-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,6,4,0 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 506407-82:
(8*5)+(7*0)+(6*6)+(5*4)+(4*0)+(3*7)+(2*8)+(1*2)=135
135 % 10 = 5
So 506407-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H2F3I/c7-3-1-4(8)6(10)5(9)2-3/h1-2H

506407-82-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-Trifluoro-2-iodobenzene

1.2 Other means of identification

Product number -
Other names Cyclohexane,1,3-didecyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:506407-82-5 SDS

506407-82-5Relevant academic research and scientific papers

Trifluoro-1,3,5-tridehydrobenzene

Venkataramani, Sugumar,Winkler, Michael,Sander, Wolfram

, p. 4888 - 4893 (2008/02/08)

(Chemical Equation Presented) Three stay, three go: Flash vacuum pyrolysis (FVP) of 1 and subsequent trapping of the products in solid argon at 3 K produces trifluoro-1,3,5-tridehydrobenzene (2). IR spectroscopy, the photochemical behavior, and quantum chemical calculations confirm that for the first time a derivative of the elusive 1,3,5-tridehydrobenzene could be isolated and spectroscopically characterized.

Generation of fluorinated m-benzyne derivatives in neon matrices

Wenk, Hans Henning,Sander, Wolfram

, p. 3927 - 3935 (2007/10/03)

The fluorinated m-didehydrobenzenes 5-H-, 5-deuterio-, 5-(trifluoromethyl)-, 5-(trimethylsilyl)-, and 5-iodo-2,4,6-trifluoro-1,3-didehydrobenzene 6b-6f were generated by UV photolysis of the corresponding 1,3-diiodobenzene derivatives 4b-4f in solid neon

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