191529-08-5

Usage

Common Uses

Flame retardant, additive in industrial and consumer products

Synthesis

Bromination of 1,3,5-benzenetrimethanol

Stability

Highly stable and heat-resistant

Flammability Reduction

Effective at reducing flammability of materials

Industries

Used in manufacturing of plastics, textiles, electronic components, construction, and automotive industries

Environmental Concerns

Persistence in the environment, potential toxicity to aquatic organisms and humans

Ongoing Research

Research aimed at minimizing risks associated with its use

Regulation

Ongoing regulation to address potential environmental and health impacts

Upstream product

• 108-67-8 1,3,5-trimethyl-benzene 
• 29165-34-2 1,3,5-tris(bromo)-2,4,6-tris(bromomethyl) benzene 
• 608-72-0 2,4,6-tribromomesitylene 
• 127-08-2 potassium acetate 
• 467420-07-1 (2,4,6-tribromobenzene-1,3,5-triyl)tris(methylene) triacetate 

Downstream Products

• 1392224-10-0 C₁₈H₃₀O₃S₃ 
• 1402134-31-9 1,3,5-tribromo-2,4,6-tri(hydroxyiminomethyl)benzene 
• 60510-14-7 1,3,5-tribromo-2,4,6-tricyanobenzene 
• 86216-69-5 2,4,6-tribromo-1,3,5-trisbenzoyl chloride 
• 86216-68-4 2,4,6-tribromo-1,3,5-benzene tricarboxylic acid 
• 191529-13-2 1,3,5-Tris-(2,2-dibromo-vinyl)-2,4,6-tris-triethylsilanylethynyl-benzene 
• 191529-12-1 1,3,5-Tris-(2,2-dibromo-vinyl)-2,4,6-tris-phenylethynyl-benzene 
• 191529-11-0 2,4,6-Tris-triethylsilanylethynyl-benzene-1,3,5-tricarbaldehyde 
• 191529-10-9 2,4,6-tris(phenylethynyl)benzene-1,3,5-tricarbaldehyde 
• 502157-79-1 1,3,5-tris(2,2-dibromo-1-ethenyl)-2,4,6-tris[(trimethylsilyl)ethynyl]benzene 
• 502157-78-0 2,4,6-tris[(trimethylsilyl)ethynyl]-1,3,5-benzenetricarbaldehyde 
• 191529-09-6 2,4,6-tribromo-1,3,5-benzenetricarboxaldehyde 

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.

A Trefoil Macrocycle Synthesized by 3-Fold Benzannulation

A new trefoil-shaped molecular architecture consisting of three conjugated macrocycles was synthesized through an unprecedented 3-fold copper catalyzed [4 + 2] benzannulation. DFT calculations indicate that the most stable conformation of this trefoil macrocycle is D3-symmetric. In agreement with the calculated results, the trefoil macrocycle in single crystals exists as a pair of enantiomers with D3-symmetry and exhibits interesting honeycomb-like supramolecular structures.

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.

En route to archimedene: Total synthesis of C3h-symmetric [7]phenylene

(Matrix presented) The total synthesis of C3h-symmetric [7]phenylene has been accomplished by triple cobalt-catalyzed cycloisomerization of an appropriate nonayne. Its spectral data are in accord with the expectations for a triply angularly fus

1,3,5 / 2,4,6-Differentiated hexaalkynylbenzenes: Absorption and fluorescence properties of a D(3h)-symmetric donor-substituted system

The synthesis of 1,3,5 / 2,4,6 differentially functionalized hexaethynylbenzene derivatives is described. Interesting solvatochromic behavior was observed for 9b in the absorption and emission spectre. A twisted intramolecular charge transfer (TICT) state in polar solvents appears to be involved.