Description

(2-Chloro-5-iodophenyl)(4-ethoxyphenyl)methanone (CAS No. 1103738-26-6) is a high-purity organic compound with the molecular formula C₁₅H₁₂ClIO₂. This iodinated and chlorinated aromatic ketone features a methanone core substituted with a 2-chloro-5-iodophenyl group and a 4-ethoxyphenyl group, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a molecular weight of 386.61 g/mol, this compound is characterized by its crystalline solid form and is typically stored under inert conditions to ensure stability. Ideal for use in cross-coupling reactions, functional group transformations, and as a building block in medicinal chemistry, this compound is supplied with comprehensive analytical data including ¹H NMR, ¹³C NMR, HPLC, and mass spectrometry for quality assurance. Suitable for researchers and scientists requiring precise and reliable reagents for advanced chemical synthesis.

Properties

• CAS Number: 1103738-26-6
• Complexity: 303
• IUPAC Name: (2-chloro-5-iodo-phenyl)-(4-ethoxyphenyl)methanone
• InChI: InChI=1S/C15H12ClIO2/c1-2-19-12-6-3-10(4-7-12)15(18)13-9-11(17)5-8-14(13)16/h3-9H,2H2,1H3
• InChI Key: BGRJXWMKCUZBIG-UHFFFAOYSA-N
• Exact Mass: 385.95705
• Molecular Formula: C15H12ClIO2
• Molecular Weight: 386.61
• SMILES: CCOC1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)I)Cl
• Topological: 26.3
• Monoisotopic Mass: 385.95705
• Synonyms: (2-chloro-5-iodophenyl)(4-ethoxyphenyl)methanone, 1103738-26-6, (5-Iodo-2-chlorophenyl)(4-ethoxyphenyl)methanone, (2-chloro-5-iodo-phenyl)-(4-ethoxyphenyl)methanone, MFCD18642360, (2-chloro-5-iodophenyl)-(4-ethoxyphenyl)methanone, C15H12ClIO2, RQX245VZQ9, SCHEMBL1934926, BGRJXWMKCUZBIG-UHFFFAOYSA-N, AKOS030527184, AC-31118, DS-19445, SY126110, DB-097249, W13129, (2-chloro-5-iodophenyl) (4-ethoxyphenyl)methanone, Methanone, (2-chloro-5-iodophenyl)(4-ethoxyphenyl)-

Application

(2-Chloro-5-iodophenyl)(4-ethoxyphenyl)methanone is widely utilized as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its reactive halogen substituents make it suitable for palladium-catalyzed cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the construction of diverse biaryl structures. Researchers also employ this compound in the development of novel drug candidates and bioactive molecules due to its versatile functional groups. Additionally, it serves as a precursor in material science for the design of advanced organic materials.

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