Cas no 875013-02-8 (4-(aminomethyl)-3-methoxyphenol)

4-(Aminomethyl)-3-methoxyphenol is a phenolic compound featuring both an aminomethyl and methoxy functional group, making it a versatile intermediate in organic synthesis and pharmaceutical applications. Its structure allows for further derivatization, enabling the production of specialized chemicals, including potential drug candidates or polymer precursors. The presence of the aminomethyl group enhances reactivity in condensation and coupling reactions, while the methoxy substituent contributes to electron-donating effects, influencing solubility and stability. This compound is particularly valuable in medicinal chemistry for designing bioactive molecules due to its balanced polarity and functional group compatibility. High purity grades ensure consistent performance in research and industrial processes.
4-(aminomethyl)-3-methoxyphenol structure
875013-02-8 structure
Product Name:4-(aminomethyl)-3-methoxyphenol
CAS No:875013-02-8
MF:C8H11NO2
MW:153.178442239761
CID:709771
PubChem ID:53404334
Update Time:2025-08-04

4-(aminomethyl)-3-methoxyphenol Chemical and Physical Properties

Names and Identifiers

    • Phenol,4-(aminomethyl)-3-methoxy-
    • 4-(aminomethyl)-3-methoxyphenol
    • 4-aminomethyl-3-methoxy-phenol
    • 4-Hydroxy-2-methoxybenzylamine
    • AKOS006285938
    • 875013-02-8
    • SCHEMBL772479
    • DNNJMMIMFXFRQA-UHFFFAOYSA-N
    • DTXSID10695365
    • FT-0722371
    • EN300-182957
    • MB05069
    • MDL: MFCD07786741
    • Inchi: 1S/C8H11NO2/c1-11-8-4-7(10)3-2-6(8)5-9/h2-4,10H,5,9H2,1H3
    • InChI Key: DNNJMMIMFXFRQA-UHFFFAOYSA-N
    • SMILES: O(C)C1C=C(C=CC=1CN)O

Computed Properties

  • Exact Mass: 153.078978594g/mol
  • Monoisotopic Mass: 153.078978594g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 119
  • 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
  • Surface Charge: 0
  • Tautomer Count: 3
  • XLogP3: 0.4
  • Topological Polar Surface Area: 55.5?2

4-(aminomethyl)-3-methoxyphenol Pricemore >>

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Additional information on 4-(aminomethyl)-3-methoxyphenol

4-(Aminomethyl)-3-methoxyphenol (CAS 875013-02-8): A Versatile Chemical Building Block for Modern Applications

4-(Aminomethyl)-3-methoxyphenol (CAS 875013-02-8) is an important aromatic compound that has gained significant attention in pharmaceutical research, material science, and specialty chemical synthesis. This methoxy-substituted phenol derivative features both phenolic hydroxyl and aminomethyl functional groups, making it a valuable intermediate for various synthetic applications.

The compound's unique molecular structure combines the reactivity of a phenolic compound with the versatility of an amine functionality. Researchers particularly value 4-(aminomethyl)-3-methoxyphenol for its ability to serve as a precursor in the synthesis of more complex molecules. Its CAS number 875013-02-8 serves as a unique identifier in chemical databases and regulatory documentation.

In pharmaceutical applications, 4-(aminomethyl)-3-methoxyphenol has shown promise as a building block for drug development. The compound's structural features make it suitable for creating molecules with potential biological activity. Recent studies have explored its use in developing novel antioxidant compounds and neuroprotective agents, addressing current healthcare challenges related to oxidative stress and neurological disorders.

The material science field has also benefited from 4-(aminomethyl)-3-methoxyphenol CAS 875013-02-8. Its dual functionality allows for incorporation into polymer systems, where it can contribute to the development of advanced materials with specific properties. Researchers are investigating its potential in creating self-healing polymers and smart coatings, responding to the growing demand for sustainable and functional materials.

From a synthetic chemistry perspective, 4-(aminomethyl)-3-methoxyphenol offers multiple reactive sites for chemical modification. The aminomethyl group can participate in condensation reactions, while the phenolic hydroxyl enables various derivatization pathways. This versatility makes the compound particularly valuable in medicinal chemistry and material design applications.

The global market for specialty chemical intermediates like 4-(aminomethyl)-3-methoxyphenol has been growing steadily, driven by increasing demand from the pharmaceutical and advanced materials sectors. Manufacturers focusing on CAS 875013-02-8 production are implementing improved synthetic routes to enhance yield and purity while reducing environmental impact, aligning with the industry's sustainability goals.

Quality control of 4-(aminomethyl)-3-methoxyphenol typically involves advanced analytical techniques such as HPLC, GC-MS, and NMR spectroscopy. These methods ensure the compound meets the stringent purity requirements for research and industrial applications. Proper storage conditions, typically in cool, dry environments protected from light, help maintain the stability of this amino phenol derivative.

Recent scientific literature highlights innovative applications of 4-(aminomethyl)-3-methoxyphenol CAS 875013-02-8 in developing bioactive molecules and functional materials. Researchers are particularly interested in its potential role in creating multifunctional compounds that address current challenges in healthcare and technology. The compound's structural features make it suitable for designing molecules with tailored properties.

For researchers working with 4-(aminomethyl)-3-methoxyphenol, understanding its physicochemical properties is crucial. The compound typically appears as a white to off-white crystalline powder with moderate solubility in common organic solvents. Its molecular weight and structural characteristics influence its behavior in various chemical reactions and applications.

The future outlook for 4-(aminomethyl)-3-methoxyphenol (CAS 875013-02-8) appears promising, with potential expansions into emerging fields such as green chemistry and bioconjugation techniques. As synthetic methodologies advance and application areas diversify, this versatile chemical intermediate is likely to maintain its importance in scientific research and industrial applications.

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