588-00-1

Basic information

• Product Name: (E)-bis[3-(trifluoromethyl)phenyl]diazene
• CAS NO: 588-00-1
• Molecular Formula: C₁₄H₈F₆N₂
• Molecular Weight: 318.2171
• Mol File: 588-00-1.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 327.5°C at 760 mmHg
• Flash Point: 151.9°C
• Density: 1.33g/cm³
• Vapor Pressure: 0.000384mmHg at 25°C
• Refractive Index: 1.484
• CAS DataBase Reference: (E)-bis[3-(trifluoromethyl)phenyl]diazene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-bis[3-(trifluoromethyl)phenyl]diazene(588-00-1)
• EPA Substance Registry System: (E)-bis[3-(trifluoromethyl)phenyl]diazene(588-00-1)

Safety Data

• Hazardous Substances Data: 588-00-1(Hazardous Substances Data)

Usage

Description

(E)-bis[3-(trifluoromethyl)phenyl]diazene, also known as difluorodiazene, is a chemical compound with the molecular formula C14H4F6N2. It is a highly reactive and unstable compound that is characterized by its double bond between the two nitrogen atoms. (E)-bis[3-(trifluoromethyl)phenyl]diazene is primarily used as a precursor in the synthesis of various organic and inorganic compounds.

Uses

Used in Chemical Synthesis:
(E)-bis[3-(trifluoromethyl)phenyl]diazene is used as a precursor in the chemical synthesis of various organic and inorganic compounds. Its reactivity and unique molecular structure make it a valuable component in the creation of new materials and substances.
Used in Rocket Propulsion Systems:
In the aerospace industry, (E)-bis[3-(trifluoromethyl)phenyl]diazene is used as a potential propellant for rocket propulsion systems. Its high reactivity and energy content contribute to its potential as a fuel source, although its unstable nature and handling challenges must be carefully managed.

Upstream product

• 98-16-8 3-trifluoromethylaniline 
• 2101-86-2 p-methylazidobenzene 
• 22001-17-8 3-trifluoromethylphenylazide 
• 351-19-9 1,2-bis(3-(trifluoromethyl)phenyl)hydrazine 
• 7664-93-9 sulfuric acid 
• 98-46-4 3-trifluoromethylnitrobenzene 

Downstream Products

• 98-16-8 3-trifluoromethylaniline 
• 535-52-4 2-fluoro-5-(trifluoromethyl)aniline 
• 324-32-3 2-methyl-7-trifluoromethylquinoline 
• 65934-71-6 (3-trifluoromethyl)-N-isopropylbenzenamine 
• 457-07-8 1,2‐bis(3‐(trifluoromethyl)phenyl)diazene 1‐oxide 
• 351-19-9 1,2-bis(3-(trifluoromethyl)phenyl)hydrazine 
• 341-58-2 2,2'-bis(trifluoromethyl)benzidine 
• 440-66-4 4,2'-bis-trifluoromethyl-biphenyl-2,4'-diyldiamine 

Relevant articles and documents

A synthetic method of aromatic azo compounds

The present invention belongs to the field of azo compound technology, discloses a method of synthesis of an aromatic azo compound. The present invention is an aromatic amine and a catalyst massager ratio 1: 0.05 ~ 0.06 mixed, at 95 ~ 110 ° C reaction 22

Synthesis of 2 - fluoro aniline compounds of the method

The invention discloses a method for synthesizing 2 - fluoro aniline compounds of the method, the method is: shown in formula Ia aniline compound of formula Ib α and β shown aniline compound as raw materials, through coupling reaction shown [...] azobenzene compound II, then the type II shown azobenzene compound with a palladium catalyst, fluorination reagent, additive, organic solvent, in the 30 - 150 °C temperature closed agitating the fluorination reaction, [...] compound of formula III, type III compounds are shown in the reaction under the action of a reducing [...] shown IV 2 - fluoro aniline compounds; this invention synthetic 2 - fluoro aniline compounds substrate wide adaptability, mild reaction conditions, the operation is simple, fluorinated and good selectivity, [...] aniline compounds is prepared by many drug molecule is an important intermediate and starting material, wide application prospects.

Application of Silicon-Initiated Water Splitting for the Reduction of Organic Substrates

The use of water as a donor for hydrogen suitable for the reduction of several important classes of organic compounds is described. It is found that the reductive water splitting can be promoted by several metalloids among which silicon shows the best efficiency. The developed methodologies were applied for the reduction of nitro compounds, N-oxides, sulfoxides, alkenes, alkynes, hydrodehalogenation as well as for the gram-scale synthesis of several substrates of industrial importance.