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Atomfair 2,6-Dimethylbenzophenone C15H14O

Description 2,6-Dimethylbenzophenone (CAS No. 1157-84-2) is a high-purity organic compound with the molecular formula C15H14O and IUPAC name (2,6-dimethylphenyl)-phenylmethanone. This crystalline solid is widely utilized in research and industrial applications due to its role as a key intermediate in organic synthesis. With a molecular weight of 210.27 g/mol, it exhibits excellent stability and is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. Our product is rigorously tested to ensure ??98% purity (GC), making it ideal for photochemistry, material science, and pharmaceutical research. Each batch is supplied with detailed analytical documentation, including NMR and HPLC data, to guarantee…

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Description

Description

2,6-Dimethylbenzophenone (CAS No. 1157-84-2) is a high-purity organic compound with the molecular formula C15H14O and IUPAC name (2,6-dimethylphenyl)-phenylmethanone. This crystalline solid is widely utilized in research and industrial applications due to its role as a key intermediate in organic synthesis. With a molecular weight of 210.27 g/mol, it exhibits excellent stability and is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. Our product is rigorously tested to ensure ??98% purity (GC), making it ideal for photochemistry, material science, and pharmaceutical research. Each batch is supplied with detailed analytical documentation, including NMR and HPLC data, to guarantee reproducibility and quality for demanding laboratory applications.

  • CAS No: 1157-84-2
  • Molecular Formula: C15H14O
  • Molecular Weight: 210.27
  • Exact Mass: 210.104465066
  • Monoisotopic Mass: 210.104465066
  • IUPAC Name: (2,6-dimethylphenyl)-phenylmethanone
  • SMILES: CC1=C(C(=CC=C1)C)C(=O)C2=CC=CC=C2
  • Synonyms: 2,6-Dimethylbenzophenone, 1139-60-2, EINECS 214-522-3, DTXSID30150608, DTXCID4073099

Application

2,6-Dimethylbenzophenone is primarily used as a photoinitiator in UV-curable coatings and inks, where it facilitates rapid polymerization under UV light exposure. It also serves as a versatile building block in the synthesis of specialty chemicals, including liquid crystals and pharmaceutical intermediates. Researchers leverage its photochemical properties for studies involving energy transfer and radical reactions in organic frameworks.

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