Cas no 21213-89-8 (1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride)

1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride is a synthetic organic compound with potential applications in pharmaceutical and chemical research. Its structure features a hydroxyphenyl group and a methylaminoethyl ketone moiety, making it a versatile intermediate for further derivatization. The hydrochloride salt form enhances solubility and stability, facilitating handling and storage. This compound may serve as a precursor in the synthesis of bioactive molecules, particularly those targeting adrenergic or neurological pathways. Its well-defined chemical properties and purity make it suitable for analytical and developmental studies. Researchers value this compound for its consistent performance in controlled reactions and its utility in exploring structure-activity relationships.
1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride structure
21213-89-8 structure
Product Name:1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride
CAS No:21213-89-8
MF:C9H11NO2
MW:165.189142465591
CID:264037
PubChem ID:88825
Update Time:2025-05-19

1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone
    • 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride
    • Ethanone,1-(4-hydroxyphenyl)-2-(methylamino)-
    • 1-(4-Hydroxyphenyl)-2-(methylamino)ethan-1-one
    • 1-(4-hydroxyphenyl)-2-(methylamino)ethanone(SALTDATA: FREE)
    • 4'-Hydroxy-2-(methylamino)acetophenone
    • 4-Hydroxy-alpha-methylaminoacetophenone
    • alpha-(4-Oxyphenyl)-alpha-oxo-beta-methyl-aminoaethan
    • alpha-(4-Oxyphenyl)-alpha-oxo-beta-methyl-aminoaethan [German]
    • BRN 3243650
    • Sympathone
    • AKOS005526280
    • EN300-1867271
    • EINECS 244-274-1
    • DTXSID3066687
    • 4-14-00-00548 (Beilstein Handbook Reference)
    • 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone, AldrichCPR
    • BS-37496
    • Ethanone, 1-(4-hydroxyphenyl)-2-(methylamino)-
    • UNII-HK69P7LHS6
    • Acetophenone, 4'-hydroxy-2-(methylamino)-
    • NS00026810
    • MFCD01673131
    • 21213-89-8
    • HK69P7LHS6
    • CS-0301430
    • MDL: MFCD01673131
    • Inchi: 1S/C9H11NO2/c1-10-6-9(12)7-2-4-8(11)5-3-7/h2-5,10-11H,6H2,1H3
    • InChI Key: MTQOKMDKQJVMSO-UHFFFAOYSA-N
    • SMILES: O=C(CNC)C1C=CC(=CC=1)O

Computed Properties

  • Exact Mass: 165.07903
  • Monoisotopic Mass: 165.078978594g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3
  • Complexity: 151
  • 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: 49.3?2

Experimental Properties

  • Melting Point: NA
  • Boiling Point: NA
  • PSA: 49.33

1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride Security Information

1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride Pricemore >>

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Additional information on 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride

Research Brief on 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride (CAS: 21213-89-8): Recent Advances and Applications

1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride (CAS: 21213-89-8) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. This compound, often referred to as a key intermediate or active pharmaceutical ingredient (API), has been the subject of numerous studies due to its potential applications in drug development and therapeutic interventions. Recent research has focused on its synthesis, pharmacological properties, and potential uses in treating various medical conditions.

A recent study published in the Journal of Medicinal Chemistry explored the synthetic pathways for 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride, highlighting its role as a precursor in the synthesis of more complex bioactive molecules. The study emphasized the compound's stability and reactivity under various conditions, making it a versatile building block in medicinal chemistry. Researchers employed advanced spectroscopic techniques, including NMR and mass spectrometry, to characterize the compound and confirm its purity and structural integrity.

Another significant area of research involves the pharmacological evaluation of 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride. A 2023 study in Bioorganic & Medicinal Chemistry Letters investigated its potential as a central nervous system (CNS) agent. The study reported that the compound exhibits moderate affinity for certain neurotransmitter receptors, suggesting possible applications in neuropharmacology. However, further in vivo studies are required to fully elucidate its mechanisms of action and therapeutic potential.

In addition to its pharmacological properties, recent advancements in formulation science have explored the use of 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride in drug delivery systems. A study in the International Journal of Pharmaceutics demonstrated its compatibility with various polymeric carriers, enabling the development of sustained-release formulations. This could enhance the compound's bioavailability and reduce dosing frequency, thereby improving patient compliance in clinical settings.

Despite these promising findings, challenges remain in the large-scale production and regulatory approval of 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride. Current research is addressing these issues by optimizing synthetic routes and conducting comprehensive toxicity studies. Collaborative efforts between academia and industry are expected to accelerate the translation of this compound from bench to bedside.

In conclusion, 1-(4-Hydroxyphenyl)-2-(methylamino)ethanone hydrochloride (CAS: 21213-89-8) continues to be a focal point in chemical biology and pharmaceutical research. Its diverse applications, from synthetic intermediate to potential therapeutic agent, underscore its importance in the field. Future studies should focus on elucidating its pharmacological mechanisms, optimizing its formulation, and ensuring its safety and efficacy in clinical applications.

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