Cas no 480439-30-3 (Benzaldehyde,2,6-dichloro-3,4-dimethoxy-)

Benzaldehyde,2,6-dichloro-3,4-dimethoxy- is a substituted benzaldehyde derivative characterized by the presence of dichloro and dimethoxy functional groups at the 2,6 and 3,4 positions, respectively. This structural configuration enhances its reactivity and selectivity, making it a valuable intermediate in organic synthesis, particularly for pharmaceuticals and agrochemicals. The electron-withdrawing chlorine atoms and electron-donating methoxy groups contribute to its unique electronic properties, facilitating applications in cross-coupling reactions and heterocyclic compound formation. Its high purity and stability under controlled conditions ensure consistent performance in demanding synthetic processes. This compound is typically handled under inert conditions to preserve its integrity.
Benzaldehyde,2,6-dichloro-3,4-dimethoxy- structure
480439-30-3 structure
Product Name:Benzaldehyde,2,6-dichloro-3,4-dimethoxy-
CAS No:480439-30-3
MF:C9H8Cl2O3
MW:235.064021110535
CID:328883
PubChem ID:16217243
Update Time:2025-06-14

Benzaldehyde,2,6-dichloro-3,4-dimethoxy- Chemical and Physical Properties

Names and Identifiers

    • Benzaldehyde,2,6-dichloro-3,4-dimethoxy-
    • 2,6-Dichloro-3,4-dimethoxybenzaldehyde
    • 569402_ALDRICH
    • ACMC-20ao9d
    • CTK8C6101
    • I01-17675
    • 480439-30-3
    • 2,6-Dichloro-3,4-dimethoxybenzaldehyde, 96%
    • SCHEMBL881433
    • AKOS015889040
    • DTXSID00584299
    • FT-0713827
    • DB-070908
    • 2 6-DICHLORO-3 4-DIMETHOXYBENZALDEHYDE&
    • MDL: MFCD05865165
    • Inchi: 1S/C9H8Cl2O3/c1-13-7-3-6(10)5(4-12)8(11)9(7)14-2/h3-4H,1-2H3
    • InChI Key: FIHJBVMZUXYWLE-UHFFFAOYSA-N
    • SMILES: ClC1=C(C=O)C(=CC(=C1OC)OC)Cl

Computed Properties

  • Exact Mass: 233.98500
  • Monoisotopic Mass: 233.9850495g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 3
  • Complexity: 201
  • 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: nothing
  • XLogP3: 2.6
  • Topological Polar Surface Area: 35.5?2

Experimental Properties

  • Density: 1.358
  • Melting Point: 115-119?°C(lit.)
  • Boiling Point: 327.7°C at 760 mmHg
  • Flash Point: 140.7°C
  • Refractive Index: 1.562
  • PSA: 35.53000
  • LogP: 2.82310

Benzaldehyde,2,6-dichloro-3,4-dimethoxy- Security Information

  • WGK Germany:3

Benzaldehyde,2,6-dichloro-3,4-dimethoxy- 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%

Benzaldehyde,2,6-dichloro-3,4-dimethoxy- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
1PlusChem
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Benzaldehyde,2,6-dichloro-3,4-dimethoxy- Related Literature

Additional information on Benzaldehyde,2,6-dichloro-3,4-dimethoxy-

Comprehensive Overview of Benzaldehyde,2,6-dichloro-3,4-dimethoxy- (CAS No. 480439-30-3)

Benzaldehyde,2,6-dichloro-3,4-dimethoxy- (CAS No. 480439-30-3) is a specialized organic compound that has garnered significant attention in the fields of synthetic chemistry, pharmaceuticals, and agrochemicals. This compound, characterized by its unique dichloro and dimethoxy substitutions, serves as a versatile intermediate in the synthesis of complex molecules. Its structural features make it particularly valuable for researchers exploring structure-activity relationships (SAR) and molecular modifications to enhance bioactivity.

In recent years, the demand for Benzaldehyde derivatives has surged due to their applications in drug discovery and material science. The compound's CAS No. 480439-30-3 is frequently searched in academic databases and chemical marketplaces, reflecting its relevance in cutting-edge research. Scientists are particularly interested in its potential role as a building block for heterocyclic compounds, which are pivotal in developing new therapeutic agents and functional materials.

One of the trending topics in organic chemistry is the exploration of sustainable synthesis methods. Researchers are investigating eco-friendly approaches to produce Benzaldehyde,2,6-dichloro-3,4-dimethoxy- with minimal environmental impact. This aligns with the global push toward green chemistry, where reducing waste and optimizing energy efficiency are paramount. The compound's chloro and methoxy groups also make it a candidate for studies on selective functionalization, a hot topic in catalysis research.

From a commercial perspective, CAS No. 480439-30-3 is often discussed in the context of custom synthesis and contract manufacturing. Companies specializing in fine chemicals are increasingly offering this compound to meet the needs of pharmaceutical and agrochemical industries. Its high purity and consistent quality are critical for ensuring reproducibility in downstream applications, a factor highly valued by R&D professionals.

The analytical characterization of Benzaldehyde,2,6-dichloro-3,4-dimethoxy- is another area of interest. Advanced techniques such as NMR spectroscopy, mass spectrometry, and HPLC are routinely employed to confirm its structure and purity. These methods are essential for compliance with regulatory standards, particularly in industries where product safety and efficacy are non-negotiable.

In summary, Benzaldehyde,2,6-dichloro-3,4-dimethoxy- (CAS No. 480439-30-3) is a compound of significant scientific and industrial importance. Its applications span multiple disciplines, and its relevance is likely to grow as research into functionalized aromatics and green synthesis continues to evolve. For researchers and industry professionals, understanding this compound's properties and potential is key to unlocking new opportunities in chemical innovation.

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