Cas no 341942-09-4 (3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde)

3-[(2-Chlorophenyl)methoxy]-4-methoxybenzaldehyde is a synthetic aromatic aldehyde featuring a benzaldehyde core substituted with a 2-chlorobenzyloxy group at the 3-position and a methoxy group at the 4-position. This compound is of interest in organic synthesis and pharmaceutical research due to its versatile reactivity, particularly as an intermediate in the preparation of more complex molecules. The presence of both electron-donating (methoxy) and electron-withdrawing (chlorobenzyloxy) substituents enhances its utility in regioselective reactions. Its well-defined structure and stability under standard conditions make it suitable for applications in medicinal chemistry and material science. The compound is typically characterized by HPLC, NMR, and mass spectrometry to ensure high purity and consistency.
3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde structure
341942-09-4 structure
Product Name:3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde
CAS No:341942-09-4
MF:C15H13ClO3
MW:276.714923620224
MDL:MFCD01012919
CID:918824
PubChem ID:3725223
Update Time:2025-10-27

3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde Chemical and Physical Properties

Names and Identifiers

    • 3-((2-Chlorobenzyl)oxy)-4-methoxybenzaldehyde
    • benzaldehyde, 3-[(2-chlorophenyl)methoxy]-4-methoxy-
    • 3-[(2-Chlorobenzyl)oxy]-4-methoxybenzaldehyde
    • 3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde
    • DTXSID40395568
    • VS-04991
    • MFCD01012919
    • STK415837
    • AKOS000202157
    • 3-(2-chloro-benzyloxy)-4-methoxy-benzaldehyde, AldrichCPR
    • 341942-09-4
    • Z25631643
    • CS-0215839
    • BBL015653
    • Oprea1_843135
    • EN300-302945
    • MDL： MFCD01012919
    • Inchi： 1S/C15H13ClO3/c1-18-14-7-6-11(9-17)8-15(14)19-10-12-4-2-3-5-13(12)16/h2-9H,10H2,1H3
    • InChI Key： JPLWJAASTJIKBC-UHFFFAOYSA-N
    • SMILES： ClC1C=CC=CC=1COC1C=C(C=O)C=CC=1OC

Computed Properties

  • Exact Mass: 276.05539
  • Monoisotopic Mass: 276.0553220g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 5
  • Complexity: 285
  • 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: 3.4
  • Topological Polar Surface Area: 35.5?2

Experimental Properties

  • PSA: 35.53

3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde Related Literature

Additional information on 3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde

Comprehensive Overview of 3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde (CAS No. 341942-09-4)

3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde (CAS No. 341942-09-4) is a specialized organic compound with significant applications in pharmaceutical and chemical research. This benzaldehyde derivative is characterized by its unique molecular structure, featuring a 2-chlorophenyl methoxy group and a 4-methoxybenzaldehyde backbone. Its CAS number 341942-09-4 serves as a critical identifier for researchers and suppliers in the global chemical market.

The compound’s synthetic versatility makes it a valuable intermediate in the development of drug candidates and fine chemicals. Recent studies highlight its potential role in designing enzyme inhibitors and receptor modulators, aligning with the growing demand for targeted therapeutics. Researchers are particularly interested in its structure-activity relationship (SAR), which could unlock novel applications in medicinal chemistry.

In the context of green chemistry, 3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde has garnered attention for its compatibility with sustainable synthesis methods. With increasing emphasis on eco-friendly processes, this compound’s potential for catalytic reduction or biocatalytic transformations is being explored. Such innovations align with the UN Sustainable Development Goals (SDGs), particularly in reducing hazardous waste.

The analytical characterization of this compound involves advanced techniques like HPLC, NMR spectroscopy, and mass spectrometry. These methods ensure high purity standards, a critical factor for pharmaceutical-grade intermediates. Suppliers often emphasize batch-to-batch consistency, addressing the needs of quality-driven industries.

Market trends indicate rising interest in custom synthesis of CAS 341942-09-4, driven by its niche applications. Frequently searched queries include "buy 3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde" and "synthesis protocol for CAS 341942-09-4," reflecting its commercial and academic relevance. Regulatory compliance, such as REACH and GMP, further underscores its safe handling and distribution.

Future research may focus on derivatization strategies to expand its utility in material science or agrochemicals. As AI-driven drug discovery accelerates, compounds like 3-[(2-chlorophenyl)methoxy]-4-methoxybenzaldehyde could play a pivotal role in virtual screening libraries. Its patent landscape also remains an area of active exploration for innovators.

In summary, 341942-09-4 represents a convergence of scientific innovation and industrial applicability. Its multidisciplinary relevance ensures sustained interest across research, development, and manufacturing sectors, making it a compound to watch in evolving chemical landscapes.

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