107934-68-9

Usage

Uses

Used in Electronics Industry:
4,4'-(9H-Fluoren-9-ylidene)bis(2-chlorobenzenamine) is used as a hardener for epoxy resins in the electronics industry. The primary amine groups in CAF readily react with the glycidyl moieties of epoxy resins, resulting in cured epoxy matrices with outstanding electronic properties. This makes it an essential component in the manufacturing of electronic devices and components that require high-performance materials.
Used in Polymer Chemistry:
In the field of polymer chemistry, 4,4'-(9H-Fluoren-9-ylidene)bis(2-chlorobenzenamine) is used as a curing agent for epoxy resins. The reaction between the amine groups and the epoxy groups leads to the formation of a cross-linked network, which enhances the mechanical and thermal properties of the resulting polymer. This makes CAF a valuable additive in the production of high-performance polymers for various applications, including aerospace, automotive, and construction industries.
Used in Composite Materials:
4,4'-(9H-Fluoren-9-ylidene)bis(2-chlorobenzenamine) is also utilized as a component in the development of advanced composite materials. The combination of CAF with epoxy resins and other reinforcing agents, such as carbon fibers or glass fibers, results in composites with improved mechanical strength, thermal stability, and electrical insulation properties. These composites find applications in various industries, including aerospace, automotive, and sports equipment manufacturing.

Flammability and Explosibility

Notclassified

Upstream product

• 486-25-9 9-fluorenone 
• 95-51-2 o-chloroaniline 
• 15499-84-0 9,9-bis(4-aminophenyl)fluorene 

Relevant academic research and scientific papers

METHOD FOR MAKING A DI(AMINOARYL)FLUORENE COMPOUND

The present invention is directed to a method for making a di(aminoaryl)fluorene compound that includes the steps of: (a) reacting a fluorenone compound according structure (I) with excess aminobenzene according to structure (II) wherein: each R1/su

9,9-bis[4-aminophenyl]fluorene derivative preparation method

The invention discloses a 9,9-bis[4-aminophenyl]fluorene derivative preparation method, which comprises: carrying out a condensation reaction on 9-fluorenone and substituted aniline at a temperature of 120-160 DEG C by using concentrated sulfuric acid as

BENZOTHIAZOLE HAVING FLUORENE SKELETON AND METHOD FOR PRODUCING THE SAME

PROBLEM TO BE SOLVED: To provide a novel 2-mercaptobenzothiazole having a fluorene skeleton which can be used as the raw material for a polybenzothiazole having a fluorene skeleton, and a method for producing the same. SOLUTION: It is found out that the reaction between a bis-o-bromoaniline having a fluorene skeleton and a xanthic acid and/or an alkali metal salt of the xanthic acid makes it possible to produce a novel 2-mercaptobenzothiazole having a fluorene skeleton with good selectivity. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Chlorination process, alkylation of products of said process and some products thereof

Compounds having acidic protons and a molecular structure which can delocalize the electron density of the conjugate base (target compounds) are chlorinated by contacting such compounds with a perchloroalkane and aqueous base in the presence of a phase transfer catalyst which is an tetraalkylammonium hydroxide. Chlorinated products, preferably gem-dichloro compounds, are produced. The gem-dichloro compounds are useful for alkylation of aromatic compounds. For instance fluorene is chlorinated to form 9,9-dichlorofluorene which is reacted with such compounds as phenol or aniline to form such compounds as 9,9-bis(hydroxyphenyl)fluorene, 9,9-bis(aminophenyl)fluorene, or 9-aminophenyl-9-chlorofluorene.

Epoxy resin curing agent, curing process and composition containing it

Epoxy resin compositions which on curing yield cured resins having a high glass transition temperature, high ductility, and low moisture pick-up sed. To obtain such cured resins, 9,9--bis(aminophenyl)fluorenes are used as cured agents.