34859-78-4

Basic information

• Product Name: Benzene, 1-(4-nitrophenoxy)-4-(trifluoromethyl)-
• CAS NO: 34859-78-4
• Molecular Formula: C13H8F3NO3
• Molecular Weight: 283.207
• Mol File: 34859-78-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(4-nitrophenoxy)-4-(trifluoromethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(4-nitrophenoxy)-4-(trifluoromethyl)-(34859-78-4)
• EPA Substance Registry System: Benzene, 1-(4-nitrophenoxy)-4-(trifluoromethyl)-(34859-78-4)

Safety Data

• Hazardous Substances Data: 34859-78-4(Hazardous Substances Data)

Upstream product

• 56-23-5 tetrachloromethane 
• 620-88-2 4-nitrophenyl phenyl ether 
• 100-02-7 4-nitro-phenol 
• 402-43-7 p-trifluoromethylphenyl bromide 
• 402-45-9 4-hydroxybenzotrifluoride 
• 100-00-5 4-chlorobenzonitrile 
• 350-46-9 4-Fluoronitrobenzene 

Downstream Products

• 57478-19-0 4-(4-trifluoromethylphenoxy)-aniline 

Relevant articles and documents

Synthesis and gas transport properties of novel functional polyimide/ZnO nanocomposite thin film membranes

In this study, the synthesis, morphology, thermal properties and gas transport of new polyimide/ZnO nanohybrid films were investigated. The novel diamine, containing functional trifluoromethyl groups, was prepared in two steps by the nucleophilic substitu

Synthesis and evaluation of aminobenzothiazoles as blockers of N- and T-type calcium channels

Both N- and T-type calcium ion channels have been implicated in pain transmission and the N-type channel is a well-validated target for the treatment of neuropathic pain. An SAR investigation of a series of substituted aminobenzothiazoles identified a subset of five compounds with comparable activity to the positive control Z160 in a FLIPR-based intracellular calcium response assay measuring potency at both CaV2.2 and CaV3.2 channels. These compounds may form the basis for the development of drug leads and tool compounds for assessing in vivo effects of variable modulation of CaV2.2 and CaV3.2 channels.

Room temperature Ullmann type C-O and C-S cross coupling of aryl halides with phenol/thiophenol catalyzed by CuO nanoparticles

C-O/C-S cross coupling of aryl halides with phenol or thiophenol was studied under ligand-free condition at room temperature over CuO nanocatalyst. The scope of the reaction was extended to various aryl halides and substituted phenols under optimized condition. In general, efficient, selective, and reusable heterogeneous nano CuO catalytic system has been developed for room temperature C-O and C-S Ullmann type cross coupling reactions.