60510-14-7

Usage

Uses

Used in Plastics Industry:
1,3,5-Benzenetricarbonitrile, 2,4,6-tribromois used as a flame retardant for enhancing the fire resistance of plastics. Its effectiveness in reducing flammability makes it a valuable component in the production of various plastic materials.
Used in Textile Industry:
In the textile industry, 1,3,5-Benzenetricarbonitrile, 2,4,6-tribromois utilized as a flame retardant to improve the fire safety of fabrics. This helps in creating textiles that are less likely to catch fire and slow the spread of flames in case of a fire incident.
Used in Electronic Components:
1,3,5-Benzenetricarbonitrile, 2,4,6-tribromois also used in the production of electronic components to reduce their flammability. This is crucial for ensuring the safety and reliability of electronic devices, as it minimizes the risk of fire hazards.

Upstream product

• 467420-07-1 (2,4,6-tribromobenzene-1,3,5-triyl)tris(methylene) triacetate 
• 86216-68-4 2,4,6-tribromo-1,3,5-benzene tricarboxylic acid 
• 86216-69-5 2,4,6-tribromo-1,3,5-trisbenzoyl chloride 
• 191529-09-6 2,4,6-tribromo-1,3,5-benzenetricarboxaldehyde 
• 191529-08-5 1,3,5-tribromo-2,4,6-tris(hydroxymethyl)benzene 
• 29165-34-2 1,3,5-tris(bromo)-2,4,6-tris(bromomethyl) benzene 
• 608-72-0 2,4,6-tribromomesitylene 
• 108-67-8 1,3,5-trimethyl-benzene 
• 1402134-31-9 1,3,5-tribromo-2,4,6-tri(hydroxyiminomethyl)benzene 

Relevant academic research and scientific papers

Interfacial synthesis of crystalline two-dimensional cyano-graphdiyne

A well-defined crystalline cyano-functionalized graphdiyne (CN-GDY) is synthesized at a liquid/liquid interface through alkyne-alkyne coupling reactions. The configurations and nanostructures of CN-GDY were well characterized by TEM, SEM, AFM, XPS, and Raman spectroscopy. HR-TEM and selected area electron diffraction (SAED) in combination with structure simulation firmly revealed a 9-fold stacking mode for CN-GDY.

Organic light-emitting diode materials

Described herein are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moiety D, each moiety D is covalently attached to either the moiety B or the moiety A, and each moiety B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D, and B are defined herein.

An efficient route to 1,3,5-triazido-2,4,6-tricyanobenzene

An efficient synthetic route starting from 1,3,5-trimethylbenzene is described for binary 1,3,5- triazido-2,4,6-tricyanobenzene. Besides 1,3,5-triazido-2,4,6-tricyanobenzene, all intermediates have been isolated and fully characterized.