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Atomfair Isobutyrophenone C10H12O

Description Isobutyrophenone (CAS No. 2040-14-4), also known as 2-methyl-1-phenylpropan-1-one, is a high-purity organic compound with the molecular formula C10H12O . This aromatic ketone is widely utilized in research and industrial applications due to its role as a versatile intermediate in organic synthesis. Its clear to pale-yellow liquid form and distinct odor make it easily identifiable in laboratory settings. Isobutyrophenone is rigorously tested for purity and consistency, ensuring optimal performance in chemical reactions, including Grignard reactions, Friedel-Crafts acylation, and as a precursor for pharmaceuticals and fragrances. Packaged under inert conditions to maintain stability, this compound is ideal for researchers requiring reliable…

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Description

Description

Isobutyrophenone (CAS No. 2040-14-4), also known as 2-methyl-1-phenylpropan-1-one, is a high-purity organic compound with the molecular formula C10H12O. This aromatic ketone is widely utilized in research and industrial applications due to its role as a versatile intermediate in organic synthesis. Its clear to pale-yellow liquid form and distinct odor make it easily identifiable in laboratory settings. Isobutyrophenone is rigorously tested for purity and consistency, ensuring optimal performance in chemical reactions, including Grignard reactions, Friedel-Crafts acylation, and as a precursor for pharmaceuticals and fragrances. Packaged under inert conditions to maintain stability, this compound is ideal for researchers requiring reliable and high-quality reagents.

  • CAS No: 2040-14-4
  • Molecular Formula: C10H12O
  • Molecular Weight: 148.20
  • Exact Mass: 148.088815002
  • Monoisotopic Mass: 148.088815002
  • IUPAC Name: 2-methyl-1-phenylpropan-1-one
  • SMILES: CC(C)C(=O)C1=CC=CC=C1
  • Synonyms: Isobutyrophenone, 611-70-1, 2-methyl-1-phenylpropan-1-one, Isopropyl phenyl ketone, 1-Propanone, 2-methyl-1-phenyl-

Application

Isobutyrophenone serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It is commonly employed in organic reactions such as nucleophilic additions and reductions due to its reactive carbonyl group. Researchers also utilize it in the development of fragrance compounds and as a building block for complex organic molecules. Its stability and reactivity make it valuable in both academic and industrial laboratories.

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