Description
1-Bromo-4-(trans-4-propylcyclohexyl)benzene (CAS No. 86579-53-5) is a high-purity organic compound with the molecular formula C15H21Br. This halogenated aromatic derivative features a bromine-substituted benzene ring linked to a trans-4-propylcyclohexyl group, offering unique steric and electronic properties for advanced synthetic applications. With a molecular weight of 281.23 g/mol, this compound is characterized by its crystalline solid form under standard conditions and is soluble in common organic solvents such as dichloromethane, toluene, and THF. Ideal for researchers in materials science and organic synthesis, it serves as a versatile intermediate for liquid crystals, pharmaceuticals, and functionalized polymers. Strict quality control ensures >98% purity (HPLC), making it suitable for sensitive reactions and high-performance applications.
Properties
- CAS Number: 86579-53-5
- Complexity: 186
- IUPAC Name: 1-bromo-4-(4-propylcyclohexyl)benzene
- InChI: InChI=1S/C15H21Br/c1-2-3-12-4-6-13(7-5-12)14-8-10-15(16)11-9-14/h8-13H,2-7H2,1H3
- InChI Key: GMZABADCQVWQPS-UHFFFAOYSA-N
- Exact Mass: 280.08266
- Molecular Formula: C15H21Br
- Molecular Weight: 281.23
- SMILES: CCCC1CCC(CC1)C2=CC=C(C=C2)Br
- Monoisotopic Mass: 280.08266
- Synonyms: 1-Bromo-4-(trans-4-propylcyclohexyl)benzene, 86579-53-5, 1-bromo-4-(4-propylcyclohexyl)benzene, 1-Bromo-4-(Trans-4-n-Propylcyclohexyl)Benzene, 167858-55-1, Benzene, 1-bromo-4-(trans-4-propylcyclohexyl)-, Benzene, 1-bromo-4-(4-propylcyclohexyl)-, SCHEMBL712896, SCHEMBL2914251, GMZABADCQVWQPS-UHFFFAOYSA-N, DTXSID401006940, STK018858, AKOS005378407, AKOS015914930, DS-4790, SB66308, DA-09466, 4-(trans-4-propylcyclohexyl)phenyl bromide, DB-019079, CS-0152579, 1-(trans-4-n-propylcyclohexyl)-4-bromobenzene, D84149
Application
1-Bromo-4-(trans-4-propylcyclohexyl)benzene is widely utilized as a key intermediate in the synthesis of liquid crystal materials, particularly for display technologies. Its rigid cyclohexylbenzene core and bromine substituent enable precise functionalization in organic electronic and photonic devices. Researchers also employ this compound in cross-coupling reactions (e.g., Suzuki-Miyaura) to create advanced aromatic architectures for optoelectronic applications. Additionally, it serves as a building block for pharmaceutical candidates targeting CNS disorders due to its lipophilic character.
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