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TCI

CAS 586-37-8

3'-Methoxyacetophenone TCI M0104

3'-Methoxyacetophenone TCI M0104

Chemical Identity

CAS No.
586-37-8
PubChem
CID 11460·SID 87572211
Formula
C9H10O2
Molecular weight
150.17 g/mol
Purity
>97.0%(GC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-(3-methoxyphenyl)ethanone
SMILES
CC(=O)C1=CC(=CC=C1)OC
InChIKey
BAYUSCHCCGXLAY-UHFFFAOYSA-N
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3'-Methoxyacetophenone is a chemical compound widely used as a building block in the synthesis of complex organic compounds. It plays a crucial role in various chemical reactions involving substitution and electrophilic mechanisms. As a fundamental compound in organic chemistry, it is essential for the development of new substances, including pharmaceuticals, industrial chemicals, and precursors for heterocyclic compounds. Its stable molecular structure and moderate reactivity make it a versatile reagent in laboratory settings.

This compound is characterized by its presence of a methoxy group and a phenyl group, which enable it to participate in a wide range of chemical reactions. These functional groups contribute to its reactivity, making it suitable for reactions such as Friedel-Crafts, substitution, and condensation. The combination of these properties allows it to be a valuable tool for chemists seeking to create new molecular structures. Its chemical versatility supports its use in both academic and industrial research environments.

In Indonesian laboratories, 3'-Methoxyacetophenone is extensively used by researchers and educational institutions for research and development purposes. Its relevance spans across organic chemistry, pharmaceutical development, and material science. The compound is particularly useful for applications requiring precise chemical synthesis and structural modification. Its availability and reliability make it a preferred choice for laboratory work in Indonesia.

  • Synthesis of heterocyclic compounds for the development of new pharmaceuticals due to its reactivity and structural versatility.
  • Facilitation of Friedel-Crafts reactions in the creation of aromatic compounds through its phenyl group and electrophilic properties.
  • Contribution to the development of industrial chemicals by enabling the synthesis of complex organic molecules with functional groups.
  • Support for material science research by providing a building block for the creation of advanced chemical structures.
  • Use in academic research settings for teaching and experimental purposes due to its stability and predictable chemical behavior.

Brand TCI
CAS number 586-37-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid or liquid depending on the specific product variant
Storage Store in a cool, dry place away from direct sunlight and incompatible materials

3'-Methoxyacetophenone should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a sealed container to minimize exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical reactions. General laboratory precautions include avoiding contact with incompatible substances and ensuring proper ventilation when handling. The compound should be kept away from heat sources and direct sunlight to preserve its chemical integrity. Proper labeling and storage conditions are essential to ensure safe handling and long-term usability in laboratory settings.

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