106418-67-1

Basic information

• Product Name: 1-BROMO-4-DECYLBENZENE
• Synonyms: 4-DECYLBROMOBENZENE;4-N-DECYLBROMOBENZENE;1-BROMO-4-DECYLBENZENE;1-BROMO-4-N-DECYLBENZENE;4-Bromo-1-decylbenzene;4-Decyl-1-bromobenzene;Benzene,1-bromo-4-decyl-
• CAS NO: 106418-67-1
• Molecular Formula: C₁₆H₂₅Br
• Molecular Weight: 297.27
• Product Categories: 4-Alkylbromobenzenes (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials
• Mol File: 106418-67-1.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 346℃
• Flash Point: 206℃
• Appearance: Colorless to pale yellow/Liquid
• Density: 1.099
• Vapor Pressure: 0.000119mmHg at 25°C
• Refractive Index: 1.5110
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-BROMO-4-DECYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMO-4-DECYLBENZENE(106418-67-1)
• EPA Substance Registry System: 1-BROMO-4-DECYLBENZENE(106418-67-1)

Safety Data

• Hazardous Substances Data: 106418-67-1(Hazardous Substances Data)

Usage

General Description

1-Bromo-4-decylbenzene is a chemical compound with the molecular formula C16H25Br. It is a brominated derivative of decylbenzene, which is a hydrocarbon with a 10-carbon alkyl chain attached to a benzene ring. 1-Bromo-4-decylbenzene is widely used in organic synthesis and as a building block in the production of various compounds. It is also used as an intermediate in the manufacturing of pharmaceuticals and agrochemicals. This chemical is a colorless to light yellow liquid and is considered to be a hazardous substance, as it can cause irritation to the skin, eyes, and respiratory system upon exposure. Proper safety precautions should be taken when handling and using 1-Bromo-4-decylbenzene to prevent any potential health risks.

InChI:InChI=1/C16H25Br/c1-2-3-4-5-6-7-8-9-10-15-11-13-16(17)14-12-15/h11-14H,2-10H2,1H3

Upstream product

• 106-37-6 1.4-dibromobenzene 
• 17049-50-2 n-decyl magnesium bromide 
• 104-72-3 decylbenzene 
• 134443-99-5 1-(4-bromophenyl)decan-1-one 
• 334-48-5 1-decanoic acid 
• 112-13-0 n-decanoyl chloride 
• 108-86-1 bromobenzene 
• 112-29-8 1-bromo dodecane 
• 108-90-7 chlorobenzene 
• 37529-30-9 4-n-decylaniline 
• 7758-89-6 copper(I) chloride 
• 30089-00-0 9-octyl-9-bora-bicyclo[3.3.1]nonane 
• 1746-28-7 1-bromo-4-(2-bromoethyl)benzene 
• 111-66-0 oct-1-ene 

Downstream Products

• 135329-95-2 C₃₄H₅₂ 
• 106418-66-0 2--1,3-dichloro-2-propanol 
• 38300-04-8 4-decylbenzoic acid 
• 170981-25-6 (4-decylphenyl)boronic acid 
• 126708-45-0 1-decyl-4-ethynylbenzene 
• 54256-43-8 4-decylbenzoyl chloride 
• 106418-63-7 2--2-(chloromethyl)oxirane 
• 106418-48-8 sym-hydroxy-16-crown-5 
• 1246263-85-3 4,8-bis(4-decylphenylethynyl)benzo[1,2-b:4,5-b']dithiophene 
• 1246263-87-5 2,6-dibromo-4,8-bis(4-decylphenylethynyl)benzo-[1,2-b:4,5-b']dithiophene 
• 744246-56-8 (2-(4-decylphenyl)ethynyl)trimethylsilane 
• 1065644-38-3 2,6-bis[2-(4-decylphenyl)ethynyl]anthracene 
• 1373359-08-0 C₁₀₈H₁₃₂N₂O₂ 

Relevant articles and documents

Synthesis of new iridium complexes and their electrophosphorescent properties in polymer light-emitting diodes

Several new iridium complexes with p-substituted 2-phenylpyridine (R-PPy) ligands have been synthesized and characterized. The complexes were incorporated into phosphorescent polymer light-emitting devices using soluble poly[1,4-bis(6′-cyano-6′-methylhept

Suzuki-miyaura cross-coupling reactions of unactivated alkyl halides catalyzed by a nickel pincer complex

A nickel(II) pincer complex, [(MeN2N)Ni-Cl], was used to catalyze alkyl-alkyl and alkyl-aryl Suzuki-Miyaura coupling reactions of unactivated alkyl halides. The coupling of 9-alkyl-9-borabicyclo[3.3.1]nonane and 9-phenyl-9-borabicyclo[3.3.1]nonane reagents with alkyl halides was achieved in modest to good yields. The reactions tolerated a variety of useful functional groups including ester, ether, furan, thioether, acetal, and Boc groups. Georg Thieme Verlag Stuttgart, New York.

Solution processable symmetric 4-alkylethynylbenzene end-capped anthracene derivatives

New candidates composed of anthracene and 4-alkylethynylbenzene end-capped oligomers for OTFTs were synthesized under Sonogashira coupling reaction conditions. All oligomers were characterized by FT-IR, mass, UV-visible, and PL emission spectrum analyses, cyclic voltammetry (CV), differential scanning calorimetry (DSC), thermal gravimetric analysis (TGA), 1H-NMR, and 13C-NMR. Investigation of their physical properties showed that the oligomers had high oxidation potential and thermal stability. Thin films of DHPEAnt and DDPEAnt were characterized by spin coating them onto Si/SiO 2 to fabricate top-contact OTFTs. The devices prepared using DHPEAnt and DDPEAnt showed hole field-effect mobilities of 4.0 × 10-3 cm2/Vs and 2.0 × 10-3 cm2/Vs, respectively, for solution-processed OTFTs.