89803-70-3

Basic information

• Product Name: 2,2'-BIS(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL
• Synonyms: 2,2'-DI(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL;2,2'-BIS(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL;2,2'-Bis(trifluoromethyl)-4,4'-diiodobiphenyl 98%;2,2'-Bis(trifluoromethyl)-4,4'-diiodobiphenyl98%
• CAS NO: 89803-70-3
• Molecular Formula: C₁₄H₆F₆I₂
• Molecular Weight: 542
• Mol File: 89803-70-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2'-BIS(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-BIS(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL(89803-70-3)
• EPA Substance Registry System: 2,2'-BIS(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL(89803-70-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• HazardClass: IRRITANT
• Hazardous Substances Data: 89803-70-3(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2,2'-BIS(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL is used as a reagent in organic synthesis for the formation of carbon-carbon bonds. Its presence facilitates the creation of these bonds, which are essential in the synthesis of various organic compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,2'-BIS(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL is utilized in the production of various drugs. Its unique structure and properties make it a valuable component in the synthesis of pharmaceuticals, contributing to the development of new and effective medications.
Used in Liquid Crystal Manufacturing:
2,2'-BIS(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL is employed in the manufacture of liquid crystals, which are crucial components in display technologies. Its properties enable the creation of liquid crystals with specific characteristics, enhancing the performance of electronic devices such as televisions, computer monitors, and smartphones.
Used in Fluorinated Organic Compounds Preparation:
As a building block, 2,2'-BIS(TRIFLUOROMETHYL)-4,4'-DIIODOBIPHENYL is used in the preparation of fluorinated organic compounds. These compounds have a wide range of applications, including in the development of new materials with unique properties and in the synthesis of specialty chemicals for various industries.

Upstream product

• 7664-93-9 sulfuric acid 
• 341-58-2 2,2'-bis(trifluoromethyl)benzidine 

Downstream Products

• 719293-36-4 (S,S)-3-{4-[3-(4'-{3-[4-(2-carboxy-2-ethoxy-ethyl)-phenoxy]-propyl}-2,2'-bis-trifluoromethyl-biphenyl-4-yl)-propoxy]-phenyl}-2-ethoxy-propionic acid 
• 719293-48-8 [4-(3-{4'-[3-(4-carboxymethoxy-3-methyl-phenylsulfanyl)-propyl]-2,2'-bis-trifluoromethyl-biphenyl-4-yl}-propylsulfanyl)-2-methyl-phenoxy]-acetic acid 
• 719293-47-7 [4-(3-{4'-[3-(4-methoxycarbonylmethoxy-3-methyl-phenylsulfanyl)-propyl]-2,2'-bis-trifluoromethyl-biphenyl-4-yl}-propylsulfanyl)-2-methyl-phenoxy]-acetic acid methyl ester 

Relevant articles and documents

Solution-processible fluorinated carbazole derivative for phosphorescent organic light-emitting diodes

A fluorinated carbazole, 9,9′-[2,2′-bis(trifluoromethyl) biphenyl-4,4′-diyl]bis(9H-carbazole) (6FCBP) was prepared, which exhibited better solubility compared to the well-known hole-transporting material 4,4′-bis(carbazol-9-yl)biphenyl (CBP). 6FCBP was employed to fabricate OLEDs by spin coating or vacuum deposition with excellent performance. Copyright

A series of CBP-derivatives as host materials for blue phosphorescent organic light-emitting diodes

We report a series of CBP-derivatives with superior thermal and electronic properties for the use as host materials for blue electrophosphorescent organic light emitting diodes. We applied a systematic variation of the substitution pattern in the 2- and 2′-position of the biphenyl unit and the 3- and 6-position of the carbazole moieties. In contrast to the crystalline parent compound CBP, all methyl and trifluoromethyl substituted derivatives show amorphous behaviour. Substitution in the 2- and 2′-position of the biphenyl causes a twisting of the phenyl rings. Hence, the degree of conjugation of the molecules is limited which leads to enlarged triplet energies of approximately 2.95 eV compared to 2.58 eV for CBP. The methyl substitution at the active 3- and 6-position of the pendant carbazole units yields materials with an electrochemically stable behaviour against oxidation. The Royal Society of Chemistry.

Novel compounds, their preparation and use

A novel class of dicarboxylic acid derivatives, the use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds and methods of treatment employing these compounds and compositions. The present compounds may be useful in the treatment and/or prevention of conditions mediated by Peroxisome Proliferator-Activated Receptors (PPAR).

DICARBOXYLIC ACID DERIVATIVES AS PPAR-AGONISTS

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