Cas no 224321-19-1 (Ethanone,2-hydroxy-1-(2-methoxyphenyl)-)

Ethanone, 2-hydroxy-1-(2-methoxyphenyl)-, is a substituted acetophenone derivative featuring both hydroxyl and methoxy functional groups on its aromatic ring. This compound is of interest in organic synthesis and pharmaceutical research due to its structural versatility, enabling its use as a precursor or intermediate in the development of more complex molecules. The presence of electron-donating groups enhances its reactivity in electrophilic aromatic substitution and other transformations. Its well-defined molecular structure allows for precise modifications, making it valuable in medicinal chemistry and material science applications. The compound is typically characterized by high purity and stability under standard storage conditions.
Ethanone,2-hydroxy-1-(2-methoxyphenyl)- structure
224321-19-1 structure
Product Name:Ethanone,2-hydroxy-1-(2-methoxyphenyl)-
CAS No:224321-19-1
MF:C9H10O3
MW:166.173902988434
MDL:MFCD07778992
CID:244686
PubChem ID:11378698
Update Time:2025-05-20

Ethanone,2-hydroxy-1-(2-methoxyphenyl)- Chemical and Physical Properties

Names and Identifiers

    • Ethanone,2-hydroxy-1-(2-methoxyphenyl)-
    • 2-hydroxy-1-(2-methoxyphenyl)ethanone
    • 2-HYDROXY-2'-METHOXYACETOPHENONE
    • 1-(2-methoxyphenyl)-2-oxidanyl-ethanone
    • Ethanone,2-hydroxy-1-(2-methoxyphenyl)
    • AC5663
    • A816199
    • 1-(2-methoxyphenyl)-2-hydroxyethanone
    • SCHEMBL1448202
    • 2-HYDROXY-2-METHOXYACETOPHENONE
    • AKOS011305900
    • DTXSID30464010
    • 224321-19-1
    • SY130983
    • 2-Hydroxy-2 inverted exclamation mark -methoxyacetophenone
    • MFCD07778992
    • FT-0644056
    • ZUHXADCMYFAQEY-UHFFFAOYSA-N
    • DB-045915
    • MDL: MFCD07778992
    • Inchi: 1S/C9H10O3/c1-12-9-5-3-2-4-7(9)8(11)6-10/h2-5,10H,6H2,1H3
    • InChI Key: ZUHXADCMYFAQEY-UHFFFAOYSA-N
    • SMILES: O(C)C1C=CC=CC=1C(CO)=O

Computed Properties

  • Exact Mass: 166.06300
  • Monoisotopic Mass: 166.062994177g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3
  • Complexity: 156
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.2
  • Topological Polar Surface Area: 46.5?2

Experimental Properties

  • PSA: 46.53000
  • LogP: 0.87020

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abcr
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2-Hydroxy-2-methoxyacetophenone; .
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Ethanone,2-hydroxy-1-(2-methoxyphenyl)- Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:224321-19-1)Ethanone,2-hydroxy-1-(2-methoxyphenyl)-
Order Number:A816199
Stock Status:in Stock
Quantity:1g/5g/10g
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 16:08
Price ($):164.0/572.0/972.0

Ethanone,2-hydroxy-1-(2-methoxyphenyl)- Related Literature

Additional information on Ethanone,2-hydroxy-1-(2-methoxyphenyl)-

Ethanone, 2-Hydroxy-1-(2-Methoxyphenyl)-: A Comprehensive Overview

Ethanone, 2-hydroxy-1-(2-methoxyphenyl)-, also known by its CAS number CAS No. 224321-19-1, is a versatile organic compound with significant applications in various fields, including pharmaceuticals, agrochemicals, and materials science. This compound has garnered attention due to its unique chemical properties and potential for further functionalization. In this article, we delve into the structural characteristics, synthesis methods, applications, and recent research advancements related to this compound.

The molecular structure of Ethanone, 2-hydroxy-1-(2-methoxyphenyl)- consists of a ketone group (C=O) attached to a hydroxyl group (-OH) and a substituted phenyl ring with a methoxy group (-OCH3). The presence of these functional groups imparts the compound with reactivity that makes it suitable for various chemical transformations. The ketone group is particularly valuable in organic synthesis as it can undergo nucleophilic additions, reductions, and other reactions to form more complex molecules.

Recent studies have explored the use of Ethanone, 2-hydroxy-1-(2-methoxyphenyl)- as an intermediate in the synthesis of bioactive compounds. For instance, researchers have utilized this compound to develop novel anti-inflammatory agents by incorporating it into heterocyclic frameworks. These findings highlight its potential in drug discovery and development.

In the field of materials science, Ethanone, 2-hydroxy-1-(2-methoxyphenyl)- has been employed as a building block for the creation of advanced polymers and coatings. Its ability to form stable bonds with other monomers makes it an attractive candidate for developing high-performance materials with tailored properties.

Moreover, the compound's methoxyphenyl group contributes to its stability under certain reaction conditions, making it suitable for large-scale industrial applications. Its synthesis involves a multi-step process that typically begins with the oxidation of an appropriate alcohol precursor followed by substitution reactions to introduce the hydroxyl and methoxy groups.

Recent advancements in green chemistry have also led to more sustainable methods for synthesizing Ethanone, 2-hydroxy-1-(2-methoxyphenyl)-. For example, researchers have developed catalysts that enable the reaction to proceed under milder conditions with higher yields and reduced environmental impact.

In conclusion, Ethanone, 2-hydroxy-1-(2-methoxyphenyl)- is a valuable compound with diverse applications across multiple disciplines. Its structural features make it an ideal starting material for creating complex molecules with unique functionalities. As research continues to uncover new possibilities for this compound, its role in advancing science and technology is expected to grow significantly.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:224321-19-1)Ethanone,2-hydroxy-1-(2-methoxyphenyl)-
A816199
Purity:99%/99%/99%
Quantity:1g/5g/10g
Price ($):164.0/572.0/972.0
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