Cas no 106579-00-4 (5-Methoxy-2-methyl-4-nitroaniline)

5-Methoxy-2-methyl-4-nitroaniline structure
106579-00-4 structure
Product Name:5-Methoxy-2-methyl-4-nitroaniline
CAS No:106579-00-4
MF:C8H10N2O3
MW:182.176601886749
MDL:MFCD00010136
CID:127223
PubChem ID:602726
Update Time:2025-11-02

5-Methoxy-2-methyl-4-nitroaniline Chemical and Physical Properties

Names and Identifiers

    • 5-Methoxy-2-methyl-4-nitroaniline
    • 3-Amino-4-methyl-6-nitro anisole
    • 5-methoxy-2-methyl-4-nitroBenzenamine
    • Benzenamine,5-methoxy-2-methyl-4-nitro-
    • 5-Methoxy-2-methyl-4-nitro-anilin
    • 5-methoxy-2-methyl-4-nitro-aniline
    • 5-methoxy-2-methyl-4-nitro-phenylamine
    • 5-Nitro-2-amino-4-methoxy-toluol
    • BB_SC-6470
    • 2-Methyl-5-(methyloxy)-4-nitroaniline
    • 5-Amino-4-methyl-2-nitroanisole
    • 5-METHOXY-2-METHYL-4-NITROANILINE, TECH., 95
    • 5-AMino-4-Methyl-2-nitroanisole[5-Methoxy-2-Methyl-4-nitroaniline]
    • 3-Amino-4-methyl-6-nitroanisole
    • 5-METHOXY-2-METHYL-4-NITROANILINE, TECH., 95%
    • PEIGETRPPZVBHT-UHFFFAOYSA-N
    • 5-methoxy-2-methyl-4-nitrophenylamine
    • Benzenamine, 5-methoxy-2-methyl-4-nitro-
    • 5-Methoxy-2-methyl-4-nitroaniline;5-Methoxy-2-methyl-4-nitroaniline
    • SCHEMBL517401
    • DTXSID30345219
    • AKOS009031480
    • CS-0128595
    • AC-7177
    • FT-0686988
    • InChI=1/C8H10N2O3/c1-5-3-7(10(11)12)8(13-2)4-6(5)9/h3-4H,9H2,1-2H
    • 106579-00-4
    • A856939
    • CS-11070
    • MFCD00010136
    • J-517679
    • MDL: MFCD00010136
    • Inchi: 1S/C8H10N2O3/c1-5-3-7(10(11)12)8(13-2)4-6(5)9/h3-4H,9H2,1-2H3
    • InChI Key: PEIGETRPPZVBHT-UHFFFAOYSA-N
    • SMILES: O(C)C1=CC(=C(C)C=C1[N+](=O)[O-])N

Computed Properties

  • Exact Mass: 182.06900
  • Monoisotopic Mass: 182.06914219g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 192
  • 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: 1.4
  • Topological Polar Surface Area: 81.1

Experimental Properties

  • Color/Form: No data avaiable
  • Density: 1.266±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 166 oC
  • Boiling Point: 346.1±25.0 °C at 760 mmHg
  • Flash Point: 182℃
  • Refractive Index: 1.589
  • Solubility: Slightly soluble (1.1 g/l) (25 o C),
  • PSA: 81.07000
  • LogP: 2.59840
  • Vapor Pressure: No data available

5-Methoxy-2-methyl-4-nitroaniline Security Information

5-Methoxy-2-methyl-4-nitroaniline Customs Data

  • HS CODE:2922299090
  • Customs Data:

    China Customs Code:

    2922299090

    Overview:

    2922299090. Other amino groups(naphthol\phenol)And ether\Esters [including their salts, Except those containing more than one oxygen-containing group]. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, The color of ethanolamine and its salt should be reported, The package of ethanolamine and its salt shall be declared

    Summary:

    2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

5-Methoxy-2-methyl-4-nitroaniline Pricemore >>

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5-Methoxy-2-methyl-4-nitroaniline Production Method

Additional information on 5-Methoxy-2-methyl-4-nitroaniline

Recent Advances in the Study of 5-Methoxy-2-methyl-4-nitroaniline (CAS: 106579-00-4)

5-Methoxy-2-methyl-4-nitroaniline (CAS: 106579-00-4) is a nitroaniline derivative that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential applications in drug development and material science. Recent studies have explored its synthesis, biological activities, and potential therapeutic uses, providing new insights into its molecular mechanisms and applications.

A recent study published in the Journal of Medicinal Chemistry investigated the antimicrobial properties of 5-Methoxy-2-methyl-4-nitroaniline. The research demonstrated that this compound exhibits potent activity against a range of Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). The study attributed this activity to the compound's ability to disrupt bacterial cell wall synthesis, highlighting its potential as a lead compound for developing new antibiotics.

In addition to its antimicrobial properties, 5-Methoxy-2-methyl-4-nitroaniline has been studied for its role in organic synthesis. A 2023 paper in Organic Letters detailed a novel synthetic route for this compound using a palladium-catalyzed coupling reaction. This method offers higher yields and improved scalability compared to traditional approaches, making it more suitable for industrial applications.

Further research has explored the compound's potential in cancer therapy. A study in Bioorganic & Medicinal Chemistry Letters reported that 5-Methoxy-2-methyl-4-nitroaniline derivatives exhibit selective cytotoxicity against certain cancer cell lines, particularly those associated with breast and lung cancers. The study suggested that these derivatives could act as inhibitors of key signaling pathways involved in tumor growth and proliferation.

Despite these promising findings, challenges remain in the development of 5-Methoxy-2-methyl-4-nitroaniline-based therapeutics. Issues such as solubility, bioavailability, and potential toxicity need to be addressed through further structural optimization and preclinical studies. Ongoing research aims to overcome these hurdles and unlock the full potential of this compound in pharmaceutical applications.

In conclusion, 5-Methoxy-2-methyl-4-nitroaniline (CAS: 106579-00-4) represents a versatile and promising compound in chemical biology and drug discovery. Its diverse biological activities and synthetic accessibility make it a valuable candidate for further investigation. Future studies should focus on optimizing its pharmacological properties and exploring its mechanisms of action in greater detail.

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