117635-23-1

Basic information

• Product Name: 1,4-dibromo-2,5-didodecylbenzene
• Synonyms: 1,4-dibromo-2,5-didodecylbenzene
• CAS NO: 117635-23-1
• Molecular Weight: 572.551
• Mol File: 117635-23-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,4-dibromo-2,5-didodecylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-dibromo-2,5-didodecylbenzene(117635-23-1)
• EPA Substance Registry System: 1,4-dibromo-2,5-didodecylbenzene(117635-23-1)

Safety Data

• Hazardous Substances Data: 117635-23-1(Hazardous Substances Data)

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

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

Downstream Products

• 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 
• 325144-77-2 4-bromo-2,5-didodecyl-benzaldehyde 
• 117635-27-5 2,5-Didodecyl-terephthalonitrile 

Relevant articles and documents

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

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

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