117635-23-1

Usage

Type of compound

Dibromobenzene derivative

Common uses

Flame retardant
Additive in lubricants and coatings

Synthesis

Multi-step reaction process involving bromination of benzene derivatives and subsequent alkylation with dodecyl groups

Thermal stability

High

Volatility

Low

Effectiveness as flame retardant

Long-lasting in various materials

Lubricant additive properties

Enhanced surface protection
Reduced friction

Environmental impact

Harmful to aquatic organisms

Bioaccumulation

May bioaccumulate in the environment

Upstream product

• 143-15-7 1-dodecylbromide 
• 15890-72-9 laurylmagnesium bromide 
• 106-46-7 para-dichlorobenzene 
• 5149-65-5 4,4'-di-n-dodecylbenzene 

Downstream Products

• 325144-77-2 4-bromo-2,5-didodecyl-benzaldehyde 
• 1110785-53-9 (2E,2'E)-dimethyl 3,3'-(2,5-didodecyl-1,4-phenylene)diacrylate 
• 117635-31-1 2,5-Didodecyl-terephthalic acid 
• 325144-96-5 C₆₈H₁₁₂ 
• 325144-92-1 (2,5-didodecyl-4-prop-1-ynyl-benzyl)-phosphonic acid diethyl ester 
• 325144-99-8 1,4-Didodecyl-2-prop-1-ynyl-5-((E)-styryl)-benzene 
• 325144-87-4 (2,5-didodecyl-4-prop-1-ynyl-phenyl)-methanol 
• 325144-80-7 2,5-didodecyl-4-prop-1-ynyl-benzaldehyde 
• 557085-67-3 2,5-didodecylterephthalaldehyde 
• 117635-27-5 2,5-Didodecyl-terephthalonitrile 

Relevant academic research and scientific papers

Two-Dimensional Chirality Transfer via On-Surface Reaction

Two-dimensional chirality transfer from self-assembled (SA) molecules to covalently bonded products was achieved via on-surface synthesis on Au(111) substrates by choosing 1,4-dibromo-2,5-didodecylbenzene (12DB) and 1,4-dibromo-2,5-ditridecylbenzene (13DB

For high-frequency devices, liquid crystal medium and compound

The present invention relates to a device for high-frequency technology, or for the microwave region and millimetre wave region of the electromagnetic spectrum, characterised in that it contains a liquid-crystal medium which consists of one or more compou

Conjugated monomers and polymers and preparation and use thereof

Disclosed are new conjugated compounds (e.g., monomers and polymers) that include ladder-type moieties which can be used for preparing semiconducting materials. Such conjugated compounds can exhibit high n-type carrier mobility and/or good current modulat

Design, synthesis, and characterization of ladder-type molecules and polymers. air-stable, solution-processable n-channel and ambipolar semiconductors for thin-film transistors via experiment and theory

The design, synthesis, and characterization of new high-performance n-channel molecular/ polymeric semiconductors that are solution-processable and air-stable is of great interest for the development of p - n junctions, bipolar transistors, and organic co

CONJUGATED MONOMERS AND POLYMERS AND PREPARATION AND USE THEREOF

Disclosed are new conjugated compounds (e.g., monomers and polymers) that include ladder-type moieties which can be used for preparing semiconducting materials. Such conjugated compounds can exhibit high n-type carrier mobility and/or good current modulat

Synthesis and characterization of electron-deficient and highly soluble (bis)indenofluorene building blocks for n-type semiconducting polymers

(Chemical Equation Presented) New electron-deficient and soluble indenofluorene-based and bisindenofluorene-based ladder-type building blocks embedding carbonyl and dicyanovinylene functionalities were synthesized, and their optical and electrochemical pr

A High-Yield Route to 2,5-Di-n-alkyl-1,4-benzenedicarboxylic Acids

A simple and inexpensive method for preparing the previously unknown 2,5-di-n-alkylterephthalic acids 5a-d in high yields is presented.The length of the alkyl chains can be varied easily (n=6,8,12,16).