Cas no 438530-82-6 (3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde)

3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde is a specialized aromatic aldehyde featuring a methoxy-substituted benzaldehyde core with a 2,6-dimethylphenoxymethyl substituent. This compound is valued for its structural versatility in organic synthesis, serving as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. The presence of both electron-donating (methoxy) and sterically hindered (2,6-dimethylphenoxy) groups enhances its utility in regioselective reactions, particularly in electrophilic aromatic substitutions or as a precursor for further functionalization. Its well-defined molecular architecture ensures consistent reactivity, making it suitable for applications requiring precise control over chemical transformations. The compound is typically supplied with high purity to meet rigorous synthetic demands.
3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde structure
438530-82-6 structure
Product Name:3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde
CAS No:438530-82-6
MF:C17H18O3
MW:270.323025226593
MDL:MFCD02055669
CID:1069783
PubChem ID:590870
Update Time:2025-06-15

3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde Chemical and Physical Properties

Names and Identifiers

    • 3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde
    • 3-(2,6-dimethylphenoxymethyl)-4-methoxybenzaldehyde
    • 3-(2,6-Dimethyl-phenoxymethyl)-4-methoxy-benzaldehyde
    • AC1LBXU9
    • AG-690
    • CTK7A6312
    • Oprea1_340182
    • Oprea1_477247
    • STK346894
    • 3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde #
    • EN300-227633
    • 3-((2,6-Dimethylphenoxy)methyl)-4-methoxybenzaldehyde
    • Benzaldehyde, 4-methoxy-3-(2,6-dimethylphenoxymethyl)-
    • DTXSID40343605
    • E84380
    • ALBB-001079
    • 438530-82-6
    • MFCD02055669
    • VS-04027
    • AG-690/15433677
    • BBL013860
    • Z275169928
    • SCHEMBL2548051
    • CS-0215157
    • 4-methoxy-3-(2,6-dimethylphenoxymethyl)-benzaldehyde
    • AKOS000304054
    • MDL： MFCD02055669
    • Inchi： 1S/C17H18O3/c1-12-5-4-6-13(2)17(12)20-11-15-9-14(10-18)7-8-16(15)19-3/h4-10H,11H2,1-3H3
    • InChI Key： CPXYVPDEEYJVDE-UHFFFAOYSA-N
    • SMILES： O(CC1C=C(C=O)C=CC=1OC)C1C(C)=CC=CC=1C

Computed Properties

  • Exact Mass: 270.12600
  • Monoisotopic Mass: 270.125594432g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 5
  • Complexity: 295
  • 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: 3.5
  • Topological Polar Surface Area: 35.5?2

Experimental Properties

  • PSA: 35.53000
  • LogP: 3.70350

3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde Security Information

  • Hazardous Material Identification： Xi
  • HazardClass：IRRITANT

3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde Customs Data

  • HS CODE：2912499000
  • Customs Data：

    China Customs Code:

    2912499000

    Overview:

    2912499000. Other aldehyde ethers\Aldehydes, phenols and aldehydes containing other oxygen-containing groups. VAT:17.0%. Tax refund rate:9.0%. Regulatory conditions:nothing. MFN tariff:5.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, Appearance of tetraformaldehyde

    Summary:

    2912499000. other aldehyde-ethers, aldehyde-phenols and aldehydes with other oxygen function. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%

3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde Pricemore >>

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3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde Related Literature

Related Categories

Additional information on 3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde

Research Brief on 3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde (CAS: 438530-82-6)

3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde (CAS: 438530-82-6) is a synthetic organic compound that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential applications in drug development and medicinal chemistry. This research brief aims to provide an overview of the latest findings related to this compound, including its synthesis, biological activity, and potential therapeutic uses.

Recent studies have focused on the synthesis and optimization of 3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde, with particular emphasis on improving yield and purity. Advanced techniques such as high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy have been employed to characterize the compound and ensure its structural integrity. These efforts are critical for its potential use as a building block in the development of novel pharmaceuticals.

In terms of biological activity, preliminary research suggests that 3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde exhibits promising pharmacological properties. In vitro studies have demonstrated its ability to modulate specific enzymatic pathways, which could be leveraged for the treatment of various diseases, including inflammatory disorders and certain types of cancer. However, further in vivo studies are required to validate these findings and assess the compound's safety and efficacy.

The compound's mechanism of action appears to involve interaction with key cellular targets, although the exact pathways remain under investigation. Researchers are particularly interested in its potential as an inhibitor or activator of specific proteins, which could open new avenues for targeted therapy. Collaborative efforts between academic institutions and pharmaceutical companies are underway to explore these possibilities.

Despite its potential, challenges remain in the development of 3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde as a therapeutic agent. Issues such as bioavailability, metabolic stability, and potential toxicity need to be addressed through rigorous preclinical testing. Additionally, the scalability of its synthesis must be optimized to meet the demands of large-scale pharmaceutical production.

In conclusion, 3-[(2,6-Dimethylphenoxy)methyl]-4-methoxybenzaldehyde represents a promising candidate for further research in the field of medicinal chemistry. Its unique structural features and biological activity make it a valuable subject of study, with potential applications in drug discovery and development. Continued investigation into its properties and mechanisms will be essential to fully realize its therapeutic potential.

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