Cas no 79294-82-9 (5-(aminomethyl)-3-methoxybenzene-1,2-diol)

5-(Aminomethyl)-3-methoxybenzene-1,2-diol is a versatile aromatic compound featuring a phenol core substituted with methoxy, hydroxyl, and aminomethyl functional groups. Its unique structure makes it valuable in organic synthesis, particularly as an intermediate for pharmaceuticals, agrochemicals, and specialty chemicals. The presence of both amino and hydroxyl groups enhances its reactivity, enabling selective modifications for complex molecular frameworks. The methoxy group contributes to stability and solubility in organic solvents, facilitating purification and handling. This compound is particularly useful in the development of bioactive molecules, where its functional groups can serve as key binding or catalytic sites. High purity and well-defined reactivity ensure consistent performance in synthetic applications.
5-(aminomethyl)-3-methoxybenzene-1,2-diol structure
79294-82-9 structure
Product Name:5-(aminomethyl)-3-methoxybenzene-1,2-diol
CAS No:79294-82-9
MF:C8H11NO3
MW:169.177842378616
CID:554695
PubChem ID:53403842
Update Time:2025-06-14

5-(aminomethyl)-3-methoxybenzene-1,2-diol Chemical and Physical Properties

Names and Identifiers

    • 1,2-Benzenediol,5-(aminomethyl)-3-methoxy-
    • 3,4-DIHYDROXY-5-METHOXYBENZYLAMINE
    • 5-(aminomethyl)-3-methoxybenzene-1,2-diol
    • AG-H-18204
    • CTK5E6656
    • SureCN7045244
    • EN300-1848236
    • 79294-82-9
    • DTXSID30695261
    • AKOS006285442
    • SCHEMBL7045244
    • MDL: MFCD07786654
    • Inchi: 1S/C8H11NO3/c1-12-7-3-5(4-9)2-6(10)8(7)11/h2-3,10-11H,4,9H2,1H3
    • InChI Key: FQXGPLOPHTVIQG-UHFFFAOYSA-N
    • SMILES: O(C)C1=C(C(=CC(CN)=C1)O)O

Computed Properties

  • Exact Mass: 169.074
  • Monoisotopic Mass: 169.074
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 142
  • 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: 75.7A^2
  • XLogP3: 0

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Additional information on 5-(aminomethyl)-3-methoxybenzene-1,2-diol

Comprehensive Overview of 5-(Aminomethyl)-3-methoxybenzene-1,2-diol (CAS No. 79294-82-9)

5-(Aminomethyl)-3-methoxybenzene-1,2-diol, with the CAS number 79294-82-9, is a chemically significant compound that has garnered attention in various research and industrial applications. This compound, often referred to by its systematic name, belongs to the class of benzene derivatives and is characterized by its unique functional groups, including an aminomethyl group and a methoxy substituent. Its molecular structure makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and specialty chemicals.

The growing interest in 5-(aminomethyl)-3-methoxybenzene-1,2-diol is driven by its potential applications in drug discovery and biomedical research. Researchers are exploring its role as a building block for neurologically active compounds, given its structural similarity to catecholamines, which are crucial in neurotransmitter synthesis. Additionally, its antioxidant properties have sparked investigations into its use in cosmetic formulations and nutraceuticals, aligning with the rising demand for natural and sustainable ingredients.

In the context of green chemistry, CAS 79294-82-9 has been studied for its potential as a biodegradable intermediate. With increasing environmental regulations, industries are seeking alternatives to traditional solvents and reagents, and this compound’s low toxicity profile positions it as a promising candidate. Furthermore, its synthesis pathways are being optimized to reduce waste and energy consumption, addressing the global push toward sustainable manufacturing.

From a market perspective, the demand for 5-(aminomethyl)-3-methoxybenzene-1,2-diol is expected to rise, particularly in regions with robust pharmaceutical and biotechnology sectors. Analysts highlight its relevance in precision medicine and personalized therapeutics, where tailored molecular structures are essential. Companies specializing in fine chemicals are investing in scalable production methods to meet this anticipated demand, ensuring consistent quality and supply chain reliability.

For researchers and industry professionals, understanding the physicochemical properties of 79294-82-9 is critical. Its solubility, stability, and reactivity under various conditions are well-documented, facilitating its integration into complex synthetic routes. Advanced analytical techniques, such as NMR spectroscopy and mass spectrometry, are routinely employed to characterize this compound, ensuring its purity and suitability for high-value applications.

In summary, 5-(aminomethyl)-3-methoxybenzene-1,2-diol (CAS No. 79294-82-9) represents a multifaceted compound with significant potential across diverse fields. Its alignment with contemporary trends in sustainability, healthcare innovation, and material science underscores its importance in modern chemistry. As research continues to uncover new applications, this compound is poised to play a pivotal role in shaping future technological advancements.

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