64248-57-3

Usage

Uses

Used in Pharmaceutical Industry:
1,2-Difluoro-3-iodo-benzene is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure allows for the creation of molecules with specific properties that can be tailored for medicinal applications.
Used in Agrochemical Industry:
In the agrochemical sector, 1,2-difluoro-3-iodo-benzene serves as an intermediate for the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness and selectivity in controlling pests and weeds.
Used in Organic Synthesis:
1,2-Difluoro-3-iodo-benzene is employed as a reagent in organic synthesis, particularly for the production of complex organic molecules. Its presence in these reactions can facilitate the formation of desired products and improve the overall efficiency of the synthesis process.
Used in Research and Development:
1,2-DIFLUORO-3-IODO-BENZENE is also utilized in research and development settings, where it can be explored for new applications and to understand its chemical properties and reactivity. This can lead to the discovery of novel uses and advancements in the field of chemistry.

InChI:InChI=1/C6H3F2I/c7-4-2-1-3-5(9)6(4)8/h1-3H

Upstream product

• 367-11-3 ortho-difluorobenzene 

Downstream Products

• 1152719-78-2 4-chloro-1-(2,3-difluorophenyl)-1H-pyrazole 
• 1262239-33-7 1,2-difluoro-3-iodobenzene diacetate 
• 859538-20-8 2,3-difluoro(methylsulfonyl)benzene 
• 333780-74-8 2,3-difluoro-5-iodobenzoic acid 
• 501433-08-5 1,2-difluoro-3,5-diiodobenzene 
• 61346-81-4 5-fluoro-1,4-dihydro-1,4-methano-naphthalene 
• 63608-69-5 5-iodobenzonorbornadiene 
• 501433-06-3 2,3-difluoro-1,4-diiodobenzene 
• 501433-05-2 2,3-difluoro-4-iodobenzoic acid 

Relevant academic research and scientific papers

Enhancing charge mobilities in selectively fluorinated oligophenyl organic semiconductors: a design approach based on experimental and computational perspectives

Fluorination can be used to tune optoelectronic properties at the molecular level. A series of oligophenyls with various difluorinations of the phenyl rings has been synthesized, crystalized, structurally resolved and computationally analyzed for charge m

Fine electronic state tuning of cobaltadithiolene complexes by substituent groups on the benzene ring

A series of 3,6- and 4,5-dihalogen-substituted 1,2-benzenedithiol (H2bdt) ligands, (3,6-X12-4,5-X22-1,2-H2bdt) (X2 = H, X1 = F (1a), Cl (1b), Br (1c); X1 = H, X2 = Cl (4)), and their cobalt complexes, [Cp?Co(3,6-X12-4,5-X22-1,2-bdt)] (X2 = H, X1 = F (2a), Cl (2b), Br (2c); X1 = H, X2 = Cl (5)), were synthesized by a modified selective thiolation reaction. The 1,2-diphenyl-substituted cobaltadithiolene complex (2d) was also synthesized. The molecular structures of all cobaltadithiolene complexes were determined by single crystal X-ray diffraction analysis. Compounds 2a, 5 and 12 showed unique packing structures with intermolecular interactions that confirmed them as the first examples of half-sandwich-type metalladithiolene complexes with a Cp? ligand. The effects of the benzene substituent type and position on the metalladithiolene ring were investigated using UV-vis spectroscopy measurements and cyclic voltammetry. The results indicate that substitution of halogen atoms at the 3 and 6 position of the benzene ring had a larger effect on the dithiolene ring than substitution at the 4 and 5 positions.

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.