Cas no 15540-90-6 (4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione)

4,7-Dimethyl-2,3-dihydro-1H-indole-2,3-dione is a heterocyclic organic compound featuring an indole backbone substituted with methyl groups at the 4 and 7 positions and a diketone moiety at the 2,3 positions. This structure imparts unique reactivity, making it a valuable intermediate in synthetic organic chemistry, particularly for the preparation of pharmaceuticals and agrochemicals. The compound’s rigid framework and functional groups allow for selective modifications, enabling the synthesis of complex molecules. Its stability under standard conditions and compatibility with various reaction conditions enhance its utility in multi-step synthesis. Researchers value this compound for its versatility in constructing nitrogen-containing heterocycles, a common motif in bioactive molecules.
4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione structure
15540-90-6 structure
Product Name:4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione
CAS No:15540-90-6
MF:C10H9NO2
MW:175.183962583542
MDL:MFCD00047217
CID:121051
PubChem ID:3264931
Update Time:2025-05-25

4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione Chemical and Physical Properties

Names and Identifiers

    • 4,7-Dimethylindoline-2,3-dione
    • 1H-Indole-2,3-dione,4,7-dimethyl-
    • 4,7-DIMETHYL ISATIN
    • 4,7-Dimethyl-1H-indole-2,3-dione
    • 4,7-dimethyl-1H-indole-2,3-dione(SALTDATA: FREE)
    • 3,6-dimethylisatin
    • 4,7-dimethyl-indole-2,3-dione
    • 4,7-Dimethyl-indolin-2,3-dion
    • 4,7-dimethyl-indoline-2,3-dione
    • Isatin-based compound,47
    • 4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione
    • A883649
    • VYRDPBOVRAVNKT-UHFFFAOYSA-N
    • DTXSID20390819
    • 15540-90-6
    • 1H-Indole-2,3-dione, 4,7-dimethyl-
    • EN300-36227
    • F0920-4749
    • CHEMBL223254
    • MFCD00047217
    • I10166
    • SCHEMBL5323338
    • AKOS000145072
    • FT-0683266
    • BDBM22827
    • Isatin-based compound, 47
    • 4,7-Dimethylisatin
    • AS-10297
    • Z247609638
    • SB64430
    • DB-022218
    • STK416216
    • ALBB-010496
    • MDL： MFCD00047217
    • Inchi： 1S/C10H9NO2/c1-5-3-4-6(2)8-7(5)9(12)10(13)11-8/h3-4H,1-2H3,(H,11,12,13)
    • InChI Key： VYRDPBOVRAVNKT-UHFFFAOYSA-N
    • SMILES： O=C1C(NC2C(C)=CC=C(C)C=21)=O

Computed Properties

  • Exact Mass: 175.06300
  • Monoisotopic Mass: 175.063
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 0
  • Complexity: 262
  • 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
  • Topological Polar Surface Area: 46.2A^2
  • XLogP3: 1.4

Experimental Properties

  • Density: 1.25
  • Refractive Index: 1.586
  • PSA: 46.17000
  • LogP: 1.57620

4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione Security Information

  • HazardClass：IRRITANT

4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione Customs Data

  • HS CODE：2933990090
  • Customs Data：

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione Pricemore >>

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4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione Suppliers

Amadis Chemical Company Limited
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Audited Supplier Audited Supplier
(CAS:15540-90-6)4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione
Order Number:A883649
Stock Status:in Stock
Quantity:100g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 11:09
Price ($):461.0

4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione Related Literature

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Additional information on 4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione

4,7-Dimethyl-2,3-Dihydro-1H-Indole-2,3-Dione

The compound 4,7-Dimethyl-2,3-Dihydro-1H-Indole-2,3-Dione (CAS No. 15540-90-6) is a unique organic molecule with significant potential in various scientific and industrial applications. This compound belongs to the class of indole derivatives, which are widely studied due to their diverse biological activities and structural versatility. The molecule is characterized by its indole skeleton with two methyl groups at the 4 and 7 positions and a diketone functionality at the 2 and 3 positions. This combination of functional groups imparts unique chemical and physical properties to the compound.

Recent studies have highlighted the importance of indole derivatives in drug discovery and material science. For instance, researchers have explored the use of 4,7-Dimethyl-2,3-Dihydro-1H-Indole-2,3-Dione in the development of new pharmaceutical agents targeting neurodegenerative diseases. The diketone moiety in the molecule has been shown to exhibit antioxidant properties, which are crucial in protecting cells from oxidative stress—a key factor in conditions like Alzheimer's and Parkinson's diseases.

In addition to its biological applications, 4,7-Dimethyl-2,3-Dihydro-1H-Indole-2,3-Dione has also been investigated for its potential in materials science. Its rigid indole structure and conjugated system make it a promising candidate for use in organic electronics. Recent research has demonstrated that this compound can be incorporated into organic semiconductors to improve their charge transport properties. This advancement could pave the way for more efficient electronic devices in the future.

The synthesis of 4,7-Dimethyl-2,3-Dihydro-1H-Indole-2,3-Dione involves a multi-step process that typically begins with the preparation of an indole derivative followed by functionalization at specific positions. One common approach involves the use of Friedl?nder annulation reactions or other cyclization techniques to construct the indole ring system. The introduction of methyl groups at the 4 and 7 positions is achieved through alkylation or substitution reactions. Researchers have optimized these steps to improve yield and purity, making large-scale production more feasible.

One of the most exciting developments involving 4,7-Dimethyl-2,3-Dihydro-1H-Indole-2,3-Dione is its role in green chemistry initiatives. Scientists have discovered that this compound can serve as a sustainable catalyst in certain organic reactions. By utilizing renewable resources and minimizing waste generation during its synthesis and application, this compound aligns with global efforts to promote environmentally friendly chemical processes.

Furthermore, indole derivatives like 4,7-Dimethyl-2,3-Dihydro-1H-Indole-2,3-Dione are being explored for their potential in agrochemicals. Preliminary studies suggest that this compound may possess pesticidal properties due to its ability to disrupt key biochemical pathways in target organisms. If validated through further research and regulatory approvals, this could offer a new avenue for sustainable pest management solutions.

In conclusion,4,7-Dimethyl

15540-90-6 (4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione) Related Products

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Amadis Chemical Company Limited
(CAS:15540-90-6)4,7-dimethyl-2,3-dihydro-1H-indole-2,3-dione
A883649
Purity:99%
Quantity:100g
Price ($):461.0
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