7639-71-6

Basic information

• Product Name: 4-(trifluoromethyl)-N-[4-(trifluoromethyl)phenyl]aniline
• Synonyms: bis(4-(trifluoromethyl)phenyl)amine
• CAS NO: 7639-71-6
• Molecular Formula: C₁₄H₉F₆N
• Molecular Weight: 305.2184
• Mol File: 7639-71-6.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 304.3°C at 760 mmHg
• Flash Point: 137.8°C
• Density: 1.371g/cm³
• Vapor Pressure: 0.000883mmHg at 25°C
• Refractive Index: 1.501
• CAS DataBase Reference: 4-(trifluoromethyl)-N-[4-(trifluoromethyl)phenyl]aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(trifluoromethyl)-N-[4-(trifluoromethyl)phenyl]aniline(7639-71-6)
• EPA Substance Registry System: 4-(trifluoromethyl)-N-[4-(trifluoromethyl)phenyl]aniline(7639-71-6)

Safety Data

• Hazardous Substances Data: 7639-71-6(Hazardous Substances Data)

Upstream product

• 402-43-7 p-trifluoromethylphenyl bromide 
• 349-97-3 4-(trifluromethyl)acetanilide 
• 455-13-0 4-Iodobenzotrifluoride 
• 402-45-9 4-hydroxybenzotrifluoride 
• 455-14-1 4-trifluoromethylphenylamine 
• 146397-87-7 p-(trifluoromethyl)phenyl trifluoromethanesulfonate 
• 98-56-6 4-chlorobenzotrifluoride 
• 128796-39-4 4-trifluoromethylphenylboronic acid 

Downstream Products

• 1217271-23-2 Bn-N(4-CF₃-C₆H₄)2 

Relevant articles and documents

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With ～429,000 deaths in 2016, malaria remains a major infectious disease where the need to treat the fever symptoms, but also to provide relevant post-treatment prophylaxis, is of major importance. An azepanylcarbazole amino alcohol is disclosed with a long- and fast-acting in vivo antiplasmodial efficacy and meets numerous attributes of a desired post-treatment chemoprophylactic antimalarial agent. The synthesis, the parasitological characterization, and the animal pharmacokinetics and pharmacodynamics of this compound are presented along with a proposed target.

ORGANIC COMPOUNDS, LIGHT EMITTING DIODE AND LIGHT EMITTING DEVICE HAVING THE COMPOUNDS

The present invention relates to an organic compound having a condensed aromatic core with a fluorene moiety and substituted with one or more functional groups having excellent hole transport properties, and a light emitting diode and a light emitting device using the same. According to the present invention, the organic compound can be introduced into a light emitting diode by using a solution process, and has a very deep HOMO energy level. When the organic compound of the present invention is applied to a hole transport layer, a band gap of the HOMO energy level between the hole transport layer and a light emitting material layer can be reduced, and thus holes and electrons can be injected into the light emitting material layer in a balanced manner. Accordingly, the light emitting diode and the light emitting device capable of low-voltage driving with higher light emitting efficiency can be implemented.COPYRIGHT KIPO 2020

Amination of Aryl Boronic Acids with Alkylnitrites: A Convenient Complement to Cu-Promoted Reductive Amination

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