133532-73-7

Usage

Physical state

Yellow crystalline solid

Uses

Precursor in the synthesis of dyes and pigments
Potential applications in the pharmaceutical industry as an intermediate in the production of various pharmaceutical compounds
Manufacturing of high-performance polymers
Reagent in organic synthesis

Toxicity

Low acute toxicity, but long-term effects on human health are not well-studied

Safety precautions

Proper safety precautions should be taken when handling and using 1,1'-OXYBIS[3-NITRO-5(TRIFLUOROMETHYL)BENZENE]

Upstream product

• 100-02-7 4-nitro-phenol 
• 401-99-0 3,5-dinitrobenzotrifluoride 
• 454-73-9 1-fluoro-3-(trifluoromethyl)-5-nitrobenzene 
• 393-75-9 4-chloro-3,5-dinitrobenzotrifluoride 

Downstream Products

• 133532-74-8 5,5'-oxy-bis[3-(trifluoromethyl)benzenamine] 
• 100-02-7 4-nitro-phenol 
• 101-63-3 bis(4-nitrophenyl)ether 
• 349-57-5 3-nitro-5-(trifluoromethyl)phenol 

Relevant academic research and scientific papers

Effect of the nucleophile structure on the relative mobility of the nitro group and fluorine atom in reactions of 3,5-dinitro- and 3-fluoro-5-nitrobenzotrifluorides with phenols in the presence of potassium carbonate

The relative mobility of the nitro group and fluorine atom in 3,5-dinitro- and 3-fluoro-5-nitrobenzofluorides was estimated by the competing reaction technique using phenols in the presence of potassium carbonate (DMF, 65-95°C). Correlation analysis of th

Nucleophilic Substitution of Nitro Group in 3,5-Dinitrobenzotrifluoride

In the reaction of 3,5-dinitrobenzotrifluoride with phenols and thiophenol in the presence of potassium carbonate, fluoride- and nitrite-ions in DMF at 25-145°C, substitution of a nitro group takes place with formation of the corresponding 3-nitro-5-R-benzotrifluorides.

Fluorinated N,N-bis-imides

This invention relates to novel fluorinated N,N-bis-imides of the formula STR1 wherein R is a bivalent radical of the formula STR2 The compounds are particularly useful as monomers in the preparation of high performance polymer.