2368-49-2

Usage

Uses

Used in Pharmaceutical Industry:
1,3,5-tribromo-2,4,6-trifluoro-benzene is used as a building block for the production of pharmaceuticals due to its ability to be incorporated into complex organic molecules. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1,3,5-tribromo-2,4,6-trifluoro-benzene is used as a precursor for the synthesis of various agrochemicals. Its halogenated nature contributes to the creation of compounds with pesticidal or herbicidal properties, enhancing crop protection.
Used in Organic Synthesis:
1,3,5-tribromo-2,4,6-trifluoro-benzene is utilized as a reagent in organic reactions, particularly in the preparation of complex organic molecules. Its presence facilitates the formation of desired products through various synthetic pathways, contributing to the advancement of organic chemistry.
Used in Materials Science and Chemical Engineering:
Due to its unique chemical structure and properties, 1,3,5-tribromo-2,4,6-trifluoro-benzene is of interest to researchers in materials science and chemical engineering. It has potential applications in the development of new materials and compounds, such as polymers, coatings, and other specialty chemicals, that can be tailored for specific performance characteristics.

InChI:InChI=1/C6Br3F3/c7-1-4(10)2(8)6(12)3(9)5(1)11

Upstream product

• 372-38-3 1,3,5-trifluorobenzene 
• 87-82-1 hexabromobenzene 
• 2265-94-3 1,3-difluoro-5-nitrobenzene 
• 372-39-4 3,5-difluoroaniline 
• 399-36-0 N-(2,4-difluoro-phenyl)-acetamide 

Downstream Products

• 107540-19-2 1,3,5-trifluoro-2,4,6-tris(p-tolylthio)benzene 
• 59831-92-4 perfluoro-1,3,5-triphenylbenzene 
• 811718-81-7 3,5-dibromotrifluorobenzene 
• 107540-21-6 1,3,5-tris(4,6-dimethyl-3-(methoxymethylthio)phenylthio)-24,6-tris(p-tolylthio)benzene 
• 107540-22-7 1,3,5-tris((4,6-dimethyl-3-mercaptophenyl)thio)-2,4,6-tris(p-tolylthio)benzene 
• 262422-64-0 C₆₀H₁₂F₃₀ 
• 519002-11-0 C₄₂Br₃F₂₇ 
• 519002-10-9 C₄₂H₃F₂₇ 

Relevant academic research and scientific papers

Strategies for the synthesis of fluorinated liquid crystal derivatives from perbromofluoroaromatic systems

The use of perbromofluorobenzene derivatives as starting materials for the synthesis of a variety of model liquid crystal systems by a combination of nucleophilic aromatic substitution, debromolithiation/trapping, dehydration and reduction processes is de

Fluorophenylborates and their use as activators in catalyst systems for olefin polymerization

A fluorophenylborate useful as an activator for an olefin polymerization catalyst is represented by the formula: [in-line-formulae]Ct+[B—(ArfRn)4]?[/in-line-formulae]where Ct+ is a cation capable of extracting an alkyl group from, or breaking a carbon-metal bond of, an organo metallic compound; Arf is a fluorophenyl group; n is 1 or 2; and each R is independently selected from a fluorophenyl group and a fluoronaphthyl group, provided that when n=1, each R group is connected at the 3-position relative the connection between the associated Arf group and the boron atom and, when n=2; the R groups are connected at the 3-position and the 5-position respectively relative the connection between the associated Arf group and the boron atom.

Process for preparation of substituted aromatic compound

A substituted aromatic compound substituted with Q is obtained by reacting a phosphazenium compound represented by formula (1) (in the formula, Q?represents an anion in a form derived by elimination of a proton from an inorganic acid, or an active hydrogen compound having an active hydrogen on an oxygen atom, a nitrogen atom or a sulfur atom; a, b, c and d, each independently, is 0 or 1, but all of them are not 0 simultaneously; and R groups represent the same or different hydrocarbon groups having 1 to 10 carbon atoms, or two Rs on each common nitrogen atom may be bonded together to form a ring structure) with a halogenated aromatic compound having halogen atoms; whereby, at least one halogen atom in the halogenated aromatic compound is substituted with Q (where, Q represents an inorganic group or an organic group in a form derived by elimination of one electron from Q?in formula (1)).

PHOTOCHEMICAL BROMINATION OF ARENES. 2. FLUOROBENZENE DERIVATIVES (1)

Photochemically induced reaction of fluorobenzene and a range of polyfluorobenzenes, both in an excess of the arene and with fluorotrichloromethane as solvent, gave isolable adducts only with fluorobenzene, the isomeric difluorobenzenes, and in very small yield with 1,3,5-trifluorobenzene.These adducts were identified by combustion analysis, mass spectrometry, and n.m.r. techniques (1H, 13C, 19F).In every case, the expected substitution products accompanied these adducts, and in the more fully fluorinated benzene derivatives substitution was the only process observed.Fluorotrichloromethane encouraged the formation of adducts, but the concurrent formation of substantial amounts of substitution products suggested that adducts are not the necessary precursors of the substitution products, in contrast with other systems.