354123-99-2

Basic information

• Product Name: 1,4-bis(2-ethylhexyloxy)-2-methylbenzene
• Synonyms: 1,4-bis(2-ethylhexyloxy)-2-methylbenzene
• CAS NO: 354123-99-2
• Molecular Weight: 348.569
• Mol File: 354123-99-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,4-bis(2-ethylhexyloxy)-2-methylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-bis(2-ethylhexyloxy)-2-methylbenzene(354123-99-2)
• EPA Substance Registry System: 1,4-bis(2-ethylhexyloxy)-2-methylbenzene(354123-99-2)

Safety Data

• Hazardous Substances Data: 354123-99-2(Hazardous Substances Data)

Upstream product

• 95-71-6 2-methylbenzene-1,4-diol 
• 78016-72-5 2-ethylhexyl 4-methylbenzenesulfonate 
• 18908-66-2 3-bromomethylheptane 

Downstream Products

• 704903-96-8 2,5-di(2'-ethylhexyloxy)-4-methylbenzaldehyde 
• 937709-54-1 1-((E)-2-{4-[(E)-2-(4-Bromo-phenyl)-vinyl]-phenyl}-vinyl)-2,5-bis-(2-ethyl-hexyloxy)-4-methyl-benzene 
• 354124-00-8 [2,5-bis-(2-ethyl-hexyloxy)-4-methyl-benzyl]-phosphonic acid diethyl ester 
• 937709-44-9 4-{(E)-2-[2,5-Bis-(2-ethyl-hexyloxy)-4-methyl-phenyl]-vinyl}-benzaldehyde 
• 357415-89-5 (E,E)-1,4-bis[4-(trimethylsilyl)ethynyl-2,5-bis(2-ethylhexyloxy)styryl]-2-(3,7-dimethyloctyloxy)-5-methoxybezene 
• 357415-88-4 (E,E)-1,4-bis[4-bromo-2,5-bis(2-ethylhexyloxy)styryl]-2-(3,7-dimethyloctyloxy)-5-methoxybezene 
• 958007-17-5 4-{2,5-bis(2-ethylhexyloxy)-4-[(E)-2-(5-bromothiophen-2-yl)vinyl]styryl}-N,N-diethylphenylamine 
• 958007-19-7 5-{2,5-bis(2-ethylhexyloxy)-4-[4-(diethylamino)styryl]styryl}thiophene-2-carbaldehyde 
• 958007-15-3 4-[2,5-bis(2-ethylhexyloxy)-4-bromostyryl]-N,N-diethylphenylamine 
• 958007-16-4 2,5-bis(2-ethylhexyloxy)-4-[4-(diethylamino)styryl]benzaldehyde 
• 357396-90-8 diethyl [[2,5-bis(2-ethylhexyloxy)-4-bromophenyl]methyl]phosphonate 

Relevant articles and documents

Practical Synthesis of Vinyl-Substituted p-Phenylenevinylene Oligomers and Their Triethoxysilyl Derivatives

Luminescent semiconducting organic compounds are widely used as active layers in electro-optical devices. Apart from conjugated polymers, monodisperse oligomers also represent attractive materials. The synthesis of stilbenoid oligomers with polymerizable

Push-pull chromophore with phenylene and thiophene as conjugation bridge for electro-optic applications

We designed and synthesized a push-pull type chromophore (PT-TCF) containing phenylene and thiophene ring as a conjugation bridge. Bulky alkyl chain was substituted into the phenylene bridge to minimize the intermolecular interaction among the neighbor mo

Donor - Acceptor diblock copolymers based on PPV and C60: Synthesis, thermal properties, and morphology

An improved synthetic method to nitroxide end-capped poly(p- phenylenevinylene)s is presented. The nitroxide-functionalized PPVs are extended with a second coillike block by employing them as macroinitiators in a nitroxide-mediated radical polymerization (NMRP) of monomers like styrene, 4-chloromethylstyrene, 4-vinylpyridine, and n-butyl acrylate. The observed thermotropic properties and morphology of films based on the rod-coil diblock copolymers are identified and described. Some of the block copolymers are subsequently subjected to a coupling with C60 to incorporate electron-accepting properties into these PPV-based diblock copolymers. For this, a statistical copolymer built from styrene and azidomethylstyrene was used as the second coillike block, making it possible to adjust the built-in ratio of C60. The morphology and thermotropic properties of films prepared with these diblock copolymers are investigated.