Description
1-Bromo-4-(2-ethylhexyl)benzene (CAS No. 883903-22-8) is a high-purity aromatic brominated compound with the molecular formula C14H21Br. This specialized chemical features a benzene ring substituted with a bromine atom at the 1-position and a 2-ethylhexyl group at the 4-position, offering unique reactivity and solubility properties. Ideal for advanced organic synthesis, this compound is rigorously tested to meet the highest standards of purity and consistency, ensuring reliable performance in research and industrial applications. Supplied in sealed containers under inert conditions to maintain stability, it is suitable for use in pharmaceuticals, material science, and specialty chemical development. Each batch is accompanied by comprehensive analytical data including GC/MS, NMR, and HPLC for quality assurance.
Properties
- CAS Number: 883903-22-8
- Complexity: 147
- IUPAC Name: 1-bromo-4-(2-ethylhexyl)benzene
- InChI: InChI=1S/C14H21Br/c1-3-5-6-12(4-2)11-13-7-9-14(15)10-8-13/h7-10,12H,3-6,11H2,1-2H3
- InChI Key: XLINASZRJNZCAK-UHFFFAOYSA-N
- Exact Mass: 268.08266
- Molecular Formula: C14H21Br
- Molecular Weight: 269.22
- SMILES: CCCCC(CC)CC1=CC=C(C=C1)Br
- Monoisotopic Mass: 268.08266
- Synonyms: 1-Bromo-4-(2-ethylhexyl)benzene, 4-(2-ethylhexyl)bromobenzene, 883903-22-8, SCHEMBL1498212, XLINASZRJNZCAK-UHFFFAOYSA-N, 1-bromo-4-(2-ethylhexyl)-benzene, DB-092999
Application
1-Bromo-4-(2-ethylhexyl)benzene is widely utilized as a key intermediate in the synthesis of liquid crystals and organic electronic materials. Its bulky 2-ethylhexyl group enhances solubility in non-polar solvents, making it valuable for polymer and small-molecule synthesis. Researchers also employ this compound in cross-coupling reactions, such as Suzuki-Miyaura couplings, to construct complex aromatic systems. Additionally, it serves as a precursor for surfactants and phase-transfer catalysts due to its amphiphilic structure.
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