Description

1-(Trans-4-propylcyclohexyl)-4-iodobenzene (CAS No. 111158-11-3) is a high-purity organic compound with the molecular formula C₁₅H₂₁I. This iodinated benzene derivative features a trans-4-propylcyclohexyl group, making it a valuable intermediate in synthetic chemistry and materials science. Its IUPAC name is 1-iodo-4-(4-propylcyclohexyl)benzene, and it is characterized by its crystalline solid form, high stability, and compatibility with various organic solvents. Ideal for researchers and scientists, this compound is rigorously tested for purity and consistency, ensuring reliable performance in advanced applications such as liquid crystal synthesis, pharmaceutical intermediates, and organic electronics. Each batch is supplied with comprehensive analytical data, including HPLC, NMR, and mass spectrometry results.

Properties

• CAS Number: 111158-11-3
• Complexity: 186
• IUPAC Name: 1-iodo-4-(4-propylcyclohexyl)benzene
• InChI: InChI=1S/C15H21I/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: QBYHVVBZXPJPKK-UHFFFAOYSA-N
• Exact Mass: 328.06880
• Molecular Formula: C15H21I
• Molecular Weight: 328.23
• SMILES: CCCC1CCC(CC1)C2=CC=C(C=C2)I
• Monoisotopic Mass: 328.06880
• Synonyms: 111158-11-3, 1-(Trans-4-propylcyclohexyl)-4-iodobenzene, 1-Iodo-4-(trans-4-n-propylcyclohexyl)benzene, 860639-66-3, 1-IODO-4-(4-PROPYL-CYCLOHEXYL)-BENZENE, 1-iodo-4-(4-propylcyclohexyl)benzene, 1-Iodo-4-(trans-4-propylcyclohexyl)benzene, Benzene,1-iodo-4-(4-propylcyclohexyl)-, MFCD06658188, SCHEMBL712306, SCHEMBL712307, C15H21I, QBYHVVBZXPJPKK-JOCQHMNTSA-N, QBYHVVBZXPJPKK-UHFFFAOYSA-N, AKOS015914906, DS-15500, 4-iodo-1-(trans-4-propylcyclohexyl)benzene, CS-0152576, D84151, F20781, BENZENE,1-IODO-4-(TRANS-4-PROPYLCYCLOHEXYL)-

Application

1-(Trans-4-propylcyclohexyl)-4-iodobenzene is widely used as a key intermediate in the synthesis of liquid crystal materials for display technologies. Its unique structure allows for the development of advanced mesogenic compounds with tailored properties. Researchers also employ this compound in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to create complex organic architectures. Additionally, it serves as a precursor in the preparation of pharmaceutical agents and functional materials for optoelectronic devices.

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