Cas no 706822-63-1 (4-ethoxy-2,5-dimethylaniline)

4-Ethoxy-2,5-dimethylaniline is a substituted aniline derivative characterized by its ethoxy and methyl functional groups at the 4-, 2-, and 5-positions of the benzene ring. This compound serves as a versatile intermediate in organic synthesis, particularly in the production of dyes, pharmaceuticals, and agrochemicals. Its structural features enhance reactivity and selectivity in electrophilic substitution and coupling reactions. The ethoxy group contributes to improved solubility in organic solvents, while the methyl substituents influence steric and electronic properties, making it valuable for tailored synthetic applications. High purity grades ensure consistent performance in research and industrial processes. Proper handling is advised due to potential sensitivity to light and air.
4-ethoxy-2,5-dimethylaniline structure
4-ethoxy-2,5-dimethylaniline structure
Product Name:4-ethoxy-2,5-dimethylaniline
CAS No:706822-63-1
MF:C10H15NO
MW:165.232202768326
MDL:MFCD14537747
CID:557707
PubChem ID:20109522
Update Time:2025-11-02

4-ethoxy-2,5-dimethylaniline Chemical and Physical Properties

Names and Identifiers

    • Benzenamine,4-ethoxy-2,5-dimethyl-
    • Benzenamine, 4-ethoxy-2,5-dimethyl- (9CI)
    • 4-ethoxy-2,5-dimethylaniline
    • 4-ethoxy-2,5-dimethylbenzenamine
    • DGFGRYUGZNOALD-UHFFFAOYSA-N
    • MFCD14537747
    • 4-ethoxy-2,5-dimethyl-phenylamine
    • 706822-63-1
    • AKOS000345488
    • EN300-201010
    • SB76478
    • SCHEMBL653555
    • DTXSID90602552
    • CS-0238821
    • G59272
    • DB-340253
    • MDL: MFCD14537747
    • Inchi: 1S/C10H15NO/c1-4-12-10-6-7(2)9(11)5-8(10)3/h5-6H,4,11H2,1-3H3
    • InChI Key: DGFGRYUGZNOALD-UHFFFAOYSA-N
    • SMILES: O(CC)C1C=C(C)C(=CC=1C)N

Computed Properties

  • Exact Mass: 165.11545
  • Monoisotopic Mass: 165.115364102g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 138
  • 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: 2.3
  • Topological Polar Surface Area: 35.2?2

Experimental Properties

  • PSA: 35.25

4-ethoxy-2,5-dimethylaniline Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
B593365-10mg
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$ 50.00 2022-06-07
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$ 185.00 2022-06-07
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SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
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4-ethoxy-2,5-dimethylaniline Related Literature

Additional information on 4-ethoxy-2,5-dimethylaniline

4-Ethoxy-2,5-dimethylaniline (CAS No. 706822-63-1): Properties, Applications, and Market Insights

4-Ethoxy-2,5-dimethylaniline (CAS No. 706822-63-1) is a specialized aromatic amine compound with significant industrial and research applications. This substituted aniline derivative features an ethoxy group at the 4-position and methyl groups at the 2- and 5-positions, giving it unique chemical properties that make it valuable in various synthetic processes.

The compound's molecular formula is C10H15NO, with a molecular weight of 165.23 g/mol. Its structural features make it particularly interesting for pharmaceutical intermediates and dye synthesis. Recent trends in green chemistry have increased interest in this compound as researchers explore more sustainable synthetic pathways for aromatic amines.

One of the most common questions about 4-ethoxy-2,5-dimethylaniline relates to its synthesis methods. The compound can be prepared through several routes, including the ethoxylation of 2,5-dimethylaniline or through selective reduction of corresponding nitro compounds. Current research focuses on developing catalytic processes that minimize waste and improve atom economy.

In terms of physical properties, 4-ethoxy-2,5-dimethylaniline typically appears as a pale yellow to light brown crystalline solid. It has moderate solubility in organic solvents like ethanol, acetone, and dichloromethane, but limited solubility in water. These properties make it particularly useful in organic synthesis applications where controlled reactivity is desired.

The compound's primary applications include serving as a building block for azo dyes and pigment manufacturing. Its amino group allows for diazotization reactions, while the ethoxy substituent provides electronic effects that influence the color properties of resulting dyes. This makes 706822-63-1 particularly valuable in creating specialized colorants for textiles and plastics.

Another growing application area is in pharmaceutical research, where 4-ethoxy-2,5-dimethylaniline serves as a precursor for various drug candidates. The compound's structural features make it suitable for developing molecules with potential biological activity, particularly in central nervous system targeting compounds. Researchers are investigating its derivatives for various therapeutic applications.

From a market perspective, demand for substituted anilines like 4-ethoxy-2,5-dimethylaniline has been steadily increasing. The global market for fine chemicals and pharmaceutical intermediates continues to grow, driven by expanding pharmaceutical and specialty chemical industries. Manufacturers are focusing on improving production efficiency and purity levels to meet the stringent requirements of end-use applications.

Environmental considerations are increasingly important for compounds like 706822-63-1. Current research explores biodegradation pathways and eco-friendly synthesis methods to minimize environmental impact. The compound's persistence and potential ecological effects are subjects of ongoing study, with particular attention to wastewater treatment in industrial settings.

Storage and handling of 4-ethoxy-2,5-dimethylaniline require standard precautions for aromatic amines. It should be kept in tightly sealed containers away from light and oxidizing agents. While not classified as highly hazardous, proper personal protective equipment should be used when handling the compound in powder form to avoid inhalation or skin contact.

Analytical characterization of 4-ethoxy-2,5-dimethylaniline typically involves techniques such as HPLC, GC-MS, and NMR spectroscopy. Purity assessment is crucial for many applications, particularly in pharmaceutical contexts where impurity profiles must meet strict regulatory standards. Advanced analytical methods continue to improve detection limits for potential impurities.

The future outlook for 706822-63-1 appears positive, with potential growth in both traditional and emerging applications. As sustainable chemistry practices advance, we may see new synthetic routes and applications for this versatile compound. Its role in specialty chemicals and advanced materials is particularly promising for future developments.

For researchers and industrial users seeking information about 4-ethoxy-2,5-dimethylaniline, key considerations include purity specifications, synthetic methodologies, and application-specific properties. The compound's versatility ensures its continued importance in various chemical industries, while ongoing research expands its potential uses in innovative fields.

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