Cas no 22924-16-9 (2,4-Diethoxybenzaldehyde)

2,4-Diethoxybenzaldehyde is a substituted benzaldehyde derivative characterized by the presence of ethoxy groups at the 2 and 4 positions of the aromatic ring. This compound is commonly utilized as an intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its diethoxy substitution enhances electron density on the aromatic ring, influencing reactivity in condensation and substitution reactions. The aldehyde functional group provides a versatile site for further functionalization, making it valuable in heterocyclic and fine chemical synthesis. The compound exhibits moderate stability under standard conditions, though it should be stored in a cool, dry environment to minimize degradation. Its purity and consistent performance make it suitable for research and industrial applications.
2,4-Diethoxybenzaldehyde structure
2,4-Diethoxybenzaldehyde structure
Product Name:2,4-Diethoxybenzaldehyde
CAS No:22924-16-9
MF:C11H14O3
MW:194.227063655853
MDL:MFCD00995010
CID:251502
PubChem ID:24873877
Update Time:2025-05-20

2,4-Diethoxybenzaldehyde Chemical and Physical Properties

Names and Identifiers

    • 2,4-Diethoxybenzaldehyde
    • 2,4-Diethoxy-Benzaldehyde
    • Benzaldehyde,2,4-diethoxy-
    • 2,4,6-TRICHLORO BENZONITRILE
    • 2,4-Diaethoxy-benzaldehyd
    • Benzaldehyde,2,4-diethoxy
    • benzaldehyde, 2,4-diethoxy-
    • JGWAODQUCDFPGI-UHFFFAOYSA-N
    • 2,4-Diathoxybenzaldehyd
    • SP466
    • 1452AB
    • STK411552
    • BBL013992
    • VZ22565
    • TRA0024001
    • AK122367
    • ZB014130
    • SY026701
    • ST2409112
    • AB0005813
    • AKOS000113735
    • FT-0638267
    • CS-0117181
    • MFCD00995010
    • A816427
    • DTXSID00342992
    • J-014904
    • 1-(3-NITRO-2-PYRIDINYL)-2-PYRROLIDINECARBOXYLICACID
    • SCHEMBL1125718
    • 22924-16-9
    • AS-10092
    • D4847
    • 2,4-Diethoxybenzaldehyde, 98%
    • 2 pound not4-Diethoxybenzaldehyde
    • InChI=1/C11H14O3/c1-3-13-10-6-5-9(8-12)11(7-10)14-4-2/h5-8H,3-4H2,1-2H
    • DB-046023
    • ALBB-001145
    • AH-034/32841013
    • DTXCID90294072
    • MDL: MFCD00995010
    • Inchi: 1S/C11H14O3/c1-3-13-10-6-5-9(8-12)11(7-10)14-4-2/h5-8H,3-4H2,1-2H3
    • InChI Key: JGWAODQUCDFPGI-UHFFFAOYSA-N
    • SMILES: O(CC)C1C=C(C=CC=1C=O)OCC

Computed Properties

  • Exact Mass: 194.09400
  • Monoisotopic Mass: 194.094294304g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 5
  • Complexity: 170
  • 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: 2.1
  • Topological Polar Surface Area: 35.5

Experimental Properties

  • Color/Form: solid
  • Density: 1.066
  • Melting Point: 71-73?°C (lit.)
  • Boiling Point: 324.5℃/760mmHg
  • Flash Point: 141.1°C
  • Refractive Index: 1.522
  • PSA: 35.53000
  • LogP: 2.29650
  • Solubility: Not determined

2,4-Diethoxybenzaldehyde 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%

2,4-Diethoxybenzaldehyde Pricemore >>

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2,4-Diethoxybenzaldehyde Production Method

2,4-Diethoxybenzaldehyde Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:22924-16-9)2,4-Diethoxybenzaldehyde
Order Number:A816427
Stock Status:in Stock
Quantity:5.0g/10.0g
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 16:08
Price ($):255.0/423.0

Additional information on 2,4-Diethoxybenzaldehyde

2,4-Diethoxybenzaldehyde (CAS No. 22924-16-9): A Versatile Aromatic Aldehyde for Modern Applications

2,4-Diethoxybenzaldehyde (CAS No. 22924-16-9) is an important aromatic aldehyde compound with two ethoxy substituents at the 2- and 4-positions of the benzene ring. This organic chemical intermediate has gained significant attention in recent years due to its unique chemical properties and wide range of applications in various industries.

The molecular structure of 2,4-diethoxybenzaldehyde features a benzaldehyde core with ethoxy groups at specific positions, giving it distinct electronic and steric properties. This configuration makes it particularly valuable as a building block in organic synthesis, where researchers frequently search for "benzaldehyde derivatives with alkoxy substituents" or "electron-rich aromatic aldehydes".

In the pharmaceutical sector, 22924-16-9 serves as a key intermediate for synthesizing various drug candidates. Recent studies have explored its potential in developing antioxidant compounds and anti-inflammatory agents, addressing current health trends focused on oxidative stress management. The compound's structure-activity relationship makes it particularly interesting for medicinal chemistry applications.

The fragrance and flavor industry extensively utilizes 2,4-diethoxybenzaldehyde due to its pleasant aromatic characteristics. As consumers increasingly seek "natural-inspired fragrance compounds", this aldehyde derivative offers formulators a versatile ingredient for creating complex scent profiles. Its stability under various conditions makes it suitable for applications ranging from personal care products to household fragrances.

Material science researchers have discovered innovative uses for 2,4-diethoxybenzaldehyde CAS 22924-16-9 in polymer chemistry. The compound serves as a monomer or cross-linking agent in the synthesis of specialty polymers with enhanced thermal stability. This application aligns with growing industry demands for "high-performance polymer precursors" and "thermally stable materials".

In agrochemical research, 2,4-diethoxy substituted benzaldehyde has shown promise as an intermediate for crop protection agents. With increasing global focus on sustainable agriculture, researchers are investigating its derivatives as potential eco-friendly pesticide components. The compound's structural features allow for modifications that can enhance specificity while reducing environmental impact.

The synthesis of 2,4-diethoxybenzaldehyde typically involves the formylation of diethoxybenzene or selective etherification of hydroxybenzaldehyde derivatives. Process optimization remains an active area of research, particularly in developing "green chemistry approaches for aromatic aldehyde synthesis". Recent advancements have focused on catalytic methods that improve yield while minimizing waste generation.

Analytical characterization of 22924-16-9 employs standard techniques including HPLC, GC-MS, and NMR spectroscopy. Quality control protocols emphasize purity assessment, as even minor impurities can significantly affect downstream applications. The compound typically appears as a colorless to pale yellow liquid with a characteristic aromatic odor.

Storage and handling of 2,4-diethoxybenzaldehyde require standard laboratory precautions for organic compounds. While not classified as hazardous under normal conditions, proper ventilation and chemical compatibility considerations are recommended during use. Material safety data sheets provide detailed guidance for industrial-scale applications.

The market for 2,4-diethoxybenzaldehyde CAS No. 22924-16-9 has shown steady growth, driven by expanding applications in multiple industries. Suppliers often highlight its high purity grades and custom synthesis options to meet diverse customer requirements. Global trade data indicates increasing demand from pharmaceutical and specialty chemical manufacturers.

Recent patent literature reveals innovative applications of 2,4-diethoxy substituted benzaldehyde derivatives in electronic materials and advanced coatings. This aligns with technology trends toward "functional organic materials" and "specialty chemical solutions". Researchers continue to explore its potential in emerging fields such as organic electronics and energy storage systems.

Environmental considerations for 2,4-diethoxybenzaldehyde production focus on waste minimization and process efficiency. Manufacturers are increasingly adopting sustainable practices in response to industry demands for "green chemical intermediates". Life cycle assessment studies help optimize production while reducing environmental footprint.

Academic research on 22924-16-9 continues to uncover new properties and applications. Current investigations explore its potential in supramolecular chemistry and molecular recognition systems. The compound's versatility makes it a valuable tool for studying structure-property relationships in organic chemistry.

Quality specifications for 2,4-diethoxybenzaldehyde typically include parameters such as assay percentage, water content, and residual solvent levels. Different industries may require specific purity grades, with pharmaceutical applications generally demanding the highest standards. Analytical certificates accompany commercial samples to ensure compliance with customer requirements.

Future prospects for 2,4-diethoxybenzaldehyde (CAS 22924-16-9) appear promising, with potential expansions into biotechnology applications and advanced material science. As research continues to reveal new functionalities, this compound is likely to maintain its importance as a multipurpose chemical building block in scientific and industrial applications.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:22924-16-9)2,4-Diethoxybenzaldehyde
A816427
Purity:99%/99%
Quantity:5.0g/10.0g
Price ($):255.0/423.0
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