Cas no 145127-38-4 ((3-Morpholinophenyl)methanol)

(3-Morpholinophenyl)methanol is a versatile organic compound featuring both a morpholine and a hydroxymethyl functional group attached to a phenyl ring. This structure imparts unique reactivity, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The morpholine moiety enhances solubility and stability, while the hydroxymethyl group allows for further functionalization, such as oxidation or esterification. Its well-defined chemical properties ensure consistent performance in coupling reactions and heterocycle formation. The compound is typically supplied in high purity, ensuring reliable results in research and industrial applications. Its balanced lipophilicity and polarity make it particularly useful in medicinal chemistry for the development of bioactive molecules.
(3-Morpholinophenyl)methanol structure
(3-Morpholinophenyl)methanol structure
Product Name:(3-Morpholinophenyl)methanol
CAS No:145127-38-4
MF:C11H15NO2
MW:193.242303133011
MDL:MFCD07772812
CID:101861
PubChem ID:7162074
Update Time:2025-05-24

(3-Morpholinophenyl)methanol Chemical and Physical Properties

Names and Identifiers

    • (3-Morpholinophenyl)methanol
    • 3-Morpholinobenzyl Alcohol
    • 3-(MORPHOLIN-4-YL)PHENYL]METHANOL
    • Benzenemethanol,3-(4-morpholinyl)-
    • (3-morpholin-4-ylphenyl)methanol
    • [3-(Morpholin-4-yl)phenyl]methanol
    • Benzenemethanol, 3-(4-morpholinyl)-
    • 3-MorpholinobenzylAlcohol
    • MXBVALXTJZMIJB-UHFFFAOYSA-N
    • SBB091606
    • (3-morpholin-4-ylphenyl)methan-1-ol
    • TRA0031143
    • RP03914
    • SY004823
    • CS-
    • PS-3917
    • CS-0060409
    • A884665
    • F30146
    • DTXSID00428149
    • J-501228
    • MFCD07772812
    • 145127-38-4
    • AMY4594
    • SCHEMBL671148
    • AKOS006281874
    • VFA12738
    • MDL: MFCD07772812
    • Inchi: 1S/C11H15NO2/c13-9-10-2-1-3-11(8-10)12-4-6-14-7-5-12/h1-3,8,13H,4-7,9H2
    • InChI Key: MXBVALXTJZMIJB-UHFFFAOYSA-N
    • SMILES: O1CCN(C2C=CC=C(CO)C=2)CC1

Computed Properties

  • Exact Mass: 193.11000
  • Monoisotopic Mass: 193.110278721g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 169
  • 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
  • Topological Polar Surface Area: 32.7
  • XLogP3: 0.8

Experimental Properties

  • Density: 1.160±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 51 °C
  • Solubility: Dissolution (35 g/l) (25 o C),
  • PSA: 32.70000
  • LogP: 1.08050

(3-Morpholinophenyl)methanol Customs Data

  • HS CODE:2934999090
  • Customs Data:

    China Customs Code:

    2934999090

    Overview:

    2934999090. Other heterocyclic compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

(3-Morpholinophenyl)methanol Pricemore >>

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Additional information on (3-Morpholinophenyl)methanol

Comprehensive Overview of (3-Morpholinophenyl)methanol (CAS No. 145127-38-4): Properties, Applications, and Industry Insights

(3-Morpholinophenyl)methanol (CAS No. 145127-38-4) is a specialized organic compound featuring a morpholine ring and a phenylmethanol group. This structure grants it unique physicochemical properties, making it valuable in pharmaceutical intermediates, material science, and agrochemical research. The compound’s systematic name, 3-(morpholin-4-yl)benzenemethanol, reflects its precise molecular architecture, which is often searched in academic and industrial databases for synthetic applications.

In recent years, the demand for morpholine derivatives like (3-Morpholinophenyl)methanol has surged due to their role in drug discovery. Researchers frequently inquire about its synthesis methods, solubility, and stability under varying pH conditions. These queries align with trends in green chemistry, where optimizing reaction yields and reducing waste are prioritized. For instance, studies highlight its utility in cross-coupling reactions, a hotspot in catalytic process development.

The compound’s spectral data (NMR, IR, and MS) is another focal point for laboratories. Analytical chemists often search for "CAS 145127-38-4 characterization" to validate purity or troubleshoot synthesis pathways. Additionally, its logP value and hydrogen bonding capacity are critical for pharmacokinetic modeling, a topic gaining traction in AI-driven drug design platforms.

From an industrial perspective, (3-Morpholinophenyl)methanol serves as a precursor for advanced materials. Its thermal stability and compatibility with polymers are explored in coatings and adhesives. Sustainability-focused manufacturers also investigate its biodegradability, responding to global regulations on chemical footprints—a trending search term in environmental science circles.

Safety profiles of 145127-38-4 are meticulously documented, addressing common user concerns about handling protocols and storage conditions. While not classified as hazardous, proper ventilation and PPE are recommended, as with most fine chemicals. This aligns with OSHA guidelines frequently referenced in safety data sheets (SDS).

Emerging applications include electronic chemicals, where its electron-donating morpholine group enhances charge transport in organic semiconductors. Such niche uses are increasingly searched alongside terms like "conductive additives for flexible electronics," reflecting industry shifts toward wearable technology.

In summary, (3-Morpholinophenyl)methanol (CAS No. 145127-38-4) bridges multiple scientific disciplines. Its versatility in synthesis, material innovation, and compliance with eco-conscious trends ensures sustained relevance. For researchers, combining its IUPAC name with specific applications (e.g., "morpholine catalysts") yields targeted insights in literature reviews or patent searches.

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