Cas no 27164-07-4 (4-(Allyloxy)-3,5-dichlorobenzaldehyde)

4-(Allyloxy)-3,5-dichlorobenzaldehyde is a versatile aromatic aldehyde featuring both allyl ether and dichloro substituents on the benzene ring. Its molecular structure, combining reactive aldehyde functionality with an allyloxy group, makes it a valuable intermediate in organic synthesis, particularly for constructing complex heterocycles or functionalized polymers. The electron-withdrawing dichloro substituents enhance the aldehyde's electrophilicity, facilitating nucleophilic addition reactions. This compound is useful in pharmaceutical and agrochemical research, where its derivatization potential enables the development of bioactive molecules. Its stability under standard conditions and compatibility with various reaction conditions further contribute to its utility in synthetic chemistry applications.
4-(Allyloxy)-3,5-dichlorobenzaldehyde structure
27164-07-4 structure
Product Name:4-(Allyloxy)-3,5-dichlorobenzaldehyde
CAS No:27164-07-4
MF:C10H8Cl2O2
MW:231.07532119751
MDL:MFCD02604833
CID:870245
Update Time:2026-04-29

4-(Allyloxy)-3,5-dichlorobenzaldehyde Chemical and Physical Properties

Names and Identifiers

    • 4-(Allyloxy)-3,5-dichlorobenzaldehyde
    • 3,5-dichloro-4-(prop-2-en-1-yloxy)benzaldehyde
    • 3,5-dichloro-4-prop-2-enoxybenzaldehyde
    • 4-(allyloxy)-3,5-dichlorobenzaldehyde(SALTDATA: FREE)
    • Allyloxy-4-dichloro-3,5-benzaldehyd
    • MDL: MFCD02604833
    • Inchi: InChI=1S/C10H8Cl2O2/c1-2-3-14-10-8(11)4-7(6-13)5-9(10)12/h2,4-6H,1,3H2
    • InChI Key: CJJQJAJJMMBMJT-UHFFFAOYSA-N
    • SMILES: C=CCOC1=C(C=C(C=C1Cl)C=O)Cl

Computed Properties

  • Exact Mass: 229.99000
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 4

Experimental Properties

  • PSA: 26.30000
  • LogP: 3.37070

4-(Allyloxy)-3,5-dichlorobenzaldehyde Customs Data

  • HS CODE:2913000090
  • Customs Data:

    China Customs Code:

    2913000090

    Overview:

    2913000090 Item2912Other derivatives of the listed products [refer to halogenation,sulfonation,Nitrosative or nitrosative derivatives]. 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

    Summary:

    HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0%

4-(Allyloxy)-3,5-dichlorobenzaldehyde Pricemore >>

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Additional information on 4-(Allyloxy)-3,5-dichlorobenzaldehyde

Recent Advances in the Study of 4-(Allyloxy)-3,5-dichlorobenzaldehyde (CAS: 27164-07-4) in Chemical Biology and Pharmaceutical Research

The compound 4-(Allyloxy)-3,5-dichlorobenzaldehyde (CAS: 27164-07-4) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique structural properties and potential applications in drug discovery. This research briefing aims to provide a comprehensive overview of the latest studies involving this compound, focusing on its synthesis, biological activities, and potential therapeutic applications.

Recent literature highlights the role of 4-(Allyloxy)-3,5-dichlorobenzaldehyde as a key intermediate in the synthesis of various bioactive molecules. A study published in the Journal of Medicinal Chemistry (2023) demonstrated its utility in the development of novel antimicrobial agents. The compound's dichlorobenzaldehyde moiety was found to enhance the binding affinity of synthesized derivatives to bacterial enzymes, leading to improved efficacy against drug-resistant strains.

In addition to its antimicrobial potential, research has explored the compound's application in cancer therapeutics. A 2024 study in Bioorganic & Medicinal Chemistry Letters reported that derivatives of 4-(Allyloxy)-3,5-dichlorobenzaldehyde exhibited promising inhibitory effects on specific kinase pathways involved in tumor proliferation. The allyloxy group was identified as a critical structural feature for modulating selectivity and potency.

Further investigations into the compound's mechanism of action have utilized advanced computational modeling techniques. Molecular docking studies have revealed that 4-(Allyloxy)-3,5-dichlorobenzaldehyde derivatives can interact with key amino acid residues in target proteins, providing insights for structure-activity relationship (SAR) optimization. These findings are paving the way for the design of more effective and selective drug candidates.

The safety profile and pharmacokinetic properties of 4-(Allyloxy)-3,5-dichlorobenzaldehyde derivatives have also been a focus of recent research. Toxicology studies conducted in vitro and in vivo have shown that while the compound exhibits favorable bioavailability, certain structural modifications may be necessary to reduce potential hepatotoxicity. These results underscore the importance of continued optimization in the drug development process.

Looking ahead, researchers are exploring the potential of 4-(Allyloxy)-3,5-dichlorobenzaldehyde in other therapeutic areas, including neurodegenerative diseases and inflammatory disorders. Its versatility as a chemical building block, combined with ongoing advances in synthetic methodologies, positions this compound as a valuable asset in medicinal chemistry. Future studies are expected to further elucidate its full spectrum of biological activities and therapeutic potential.

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