Cas no 57583-53-6 (N,N'-Dihydroxypyromellitimide)

N,N'-Dihydroxypyromellitimide is a high-purity organic compound characterized by its pyromellitimide core functionalized with hydroxyl groups. This structure imparts excellent thermal stability and reactivity, making it suitable for applications in advanced polymer synthesis, particularly as a crosslinking agent or monomer for high-performance polyimides. Its dual hydroxyl groups enhance solubility in polar solvents, facilitating processing while maintaining robust mechanical and chemical resistance in the final material. The compound is also valued in specialty coatings and adhesives where thermal endurance and structural integrity are critical. Its well-defined molecular architecture ensures consistent performance in demanding industrial and research applications.
N,N'-Dihydroxypyromellitimide structure
N,N'-Dihydroxypyromellitimide structure
Product Name:N,N'-Dihydroxypyromellitimide
CAS No:57583-53-6
MF:C10H4N2O6
MW:248.148562431335
MDL:MFCD28334210
CID:1605288
PubChem ID:253661830
Update Time:2025-05-25

N,N'-Dihydroxypyromellitimide Chemical and Physical Properties

Names and Identifiers

    • 2,6-dihydroxypyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetrone
    • 2,6-Dihydroxypyrrolo(3,4-f)isoindole-1,3,5,7(2H,6H)-tetrone
    • N,N'-Dihydroxypyromellitimide
    • 2,6-Dihydroxypyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetraone
    • 2,6-dihydroxypyrrolo[3,4-f]isoindole-1,3,5,7-tetrone
    • 2,6-dihydroxybenzo[1,2-c:4,5-c']dipyrrole-1,3,5,7(2H,6H)-tetrone
    • 2,6-dihydroxypyromellitimide
    • 2,6-dihydroxypyrrolo[3,4-f]isoindolo-1,3,5,7(2H,6H)tetrone
    • N,N-dihydroxypyromelitimide
    • N,N'-dihydroxypyromellitic diimide
    • N,N'-dihydroxy-pyromellitimide
    • NDHPI
    • NSC6068
    • 8NNH2HXA7W
    • VBBUVIWLZBAEEF-UHFFFAOYSA-N
    • D4413
    • N,
    • MFCD28334210
    • AS-71004
    • AKOS027250852
    • H11458
    • 2,6-DIHYDROXY-1H,2H,3H,5H,6H,7H-PYRROLO[3,4-F]ISOINDOLE-1,3,5,7-TETRONE
    • 2,6-DIHYDROXYBENZO(1,2-C:4,5-C')DIPYRROLE-1,3,5,7(2H,6H)-TETRONE
    • UNII-8NNH2HXA7W
    • N,N''-Dihydroxypyromellitic diimide
    • BENZO(1,2-C:4,5-C')DIPYRROLE-1,3,5,7(2H,6H)-TETRONE, 2,6-DIHYDROXY-
    • NSC-6068
    • 57583-53-6
    • SCHEMBL43657
    • NSC 6068
    • N,N-DIHYDROXYPYROMELLITIMIDE
    • A917605
    • DTXSID30206210
    • CS-0186523
    • 1,3,5,7(2H,6H)-tetrone;
    • Benzo[1,2-c:4,5-c']dipyrrole-1,3,5,7(2H,6H)-tetrone, 2,6-dihydroxy-
    • DTXCID30128701
    • MDL: MFCD28334210
    • Inchi: 1S/C10H4N2O6/c13-7-3-1-4-6(10(16)12(18)8(4)14)2-5(3)9(15)11(7)17/h1-2,17-18H
    • InChI Key: VBBUVIWLZBAEEF-UHFFFAOYSA-N
    • SMILES: ON1C(C2C=C3C(N(C(C3=CC=2C1=O)=O)O)=O)=O

Computed Properties

  • Exact Mass: 248.00700
  • Monoisotopic Mass: 248.006936
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 0
  • Complexity: 405
  • 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: 115
  • XLogP3: -1.1

Experimental Properties

  • Density: 2.261
  • Melting Point: NA
  • Boiling Point: 687.2°C at 760 mmHg
  • Flash Point: 369.4°C
  • Refractive Index: 1.929
  • PSA: 118.60000
  • LogP: -1.61300

N,N'-Dihydroxypyromellitimide Security Information

N,N'-Dihydroxypyromellitimide 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%

N,N'-Dihydroxypyromellitimide Pricemore >>

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N,N'-Dihydroxypyromellitimide Production Method

Additional information on N,N'-Dihydroxypyromellitimide

Introduction to N,N'-Dihydroxypyromellitimide (CAS No. 57583-53-6)

N,N'-Dihydroxypyromellitimide, identified by the Chemical Abstracts Service Number (CAS No.) 57583-53-6, is a significant compound in the field of chemical biology and pharmaceutical research. This heterocyclic organic compound has garnered attention due to its unique structural properties and potential applications in drug development, particularly in modulating biological pathways associated with inflammation, oxidative stress, and cellular signaling. The molecule's distinct pyromellitic core, combined with hydroxyl functional groups, makes it a versatile scaffold for designing novel therapeutic agents.

The structural framework of N,N'-Dihydroxypyromellitimide consists of a pyromellitic acid derivative, which is a well-known moiety in various bioactive molecules. The presence of two hydroxyl groups at the N-positions enhances its reactivity, allowing for further chemical modifications that can tailor its biological activity. This adaptability has made it a subject of interest in medicinal chemistry, where researchers explore its potential as an intermediate in synthesizing more complex pharmacophores.

In recent years, there has been growing interest in N,N'-Dihydroxypyromellitimide due to its reported interactions with key enzymes and receptors involved in disease mechanisms. For instance, studies have suggested that this compound may inhibit the activity of certain proteases implicated in inflammatory responses. Additionally, its ability to scavenge reactive oxygen species has positioned it as a candidate for developing antioxidant-based therapies. These properties are particularly relevant in the context of chronic diseases where oxidative stress plays a pivotal role.

One of the most compelling aspects of N,N'-Dihydroxypyromellitimide is its potential as a lead compound for drug discovery. Researchers have been leveraging computational modeling and high-throughput screening techniques to identify derivatives with enhanced efficacy and reduced toxicity. The hydroxyl groups on the molecule provide multiple sites for chemical modification, enabling the creation of analogs with optimized pharmacokinetic profiles. Such derivatives could potentially address unmet medical needs by targeting specific pathological pathways more precisely.

The synthesis of N,N'-Dihydroxypyromellitimide itself is an intriguing aspect from a chemical perspective. Traditional synthetic routes involve multi-step organic transformations, often requiring careful control of reaction conditions to achieve high yields and purity. Advances in synthetic methodologies, such as catalytic hydrogenation and microwave-assisted reactions, have improved the efficiency of these processes. These innovations not only facilitate large-scale production but also open avenues for exploring new synthetic strategies that could further enhance accessibility to this compound.

From a biological standpoint, the investigation of N,N'-Dihydroxypyromellitimide has revealed intriguing insights into its mechanism of action. Preclinical studies have demonstrated its ability to modulate certain signaling cascades by interacting with membrane-bound receptors or intracellular enzymes. For example, it has been observed that this compound may interfere with the activation of nuclear factor kappa B (NF-κB), a transcription factor central to inflammatory processes. Such findings underscore its therapeutic potential in conditions like arthritis or autoimmune disorders.

The pharmacological profile of N,N'-Dihydroxypyromellitimide also includes notable interactions with cellular metabolism pathways. Research indicates that it may influence glucose uptake and utilization in adipose tissue and muscle cells, suggesting its relevance in managing metabolic disorders such as diabetes mellitus. Furthermore, its effects on mitochondrial function have been explored, revealing potential benefits in mitigating age-related decline in cellular energy production.

Regulatory considerations are an essential component when evaluating the clinical development prospects of N,N'-Dihydroxypyromellitimide. Given its promising preclinical data, regulatory agencies are closely monitoring ongoing studies to assess its safety and efficacy before human trials can commence. The compound's unique structure presents both opportunities and challenges in terms of formulation and delivery systems. Efforts are underway to optimize these aspects to ensure that it can be effectively administered to patients if approved for therapeutic use.

The future directions for research on N,N'-Dihydroxypyromellitimide are multifaceted and exciting. Collaborative efforts between chemists and biologists are expected to yield novel derivatives with improved pharmacological properties. Additionally, integrating machine learning algorithms into drug discovery pipelines could accelerate the identification of promising candidates derived from this scaffold. Such interdisciplinary approaches hold great promise for translating basic scientific findings into tangible therapeutic benefits.

In conclusion,N,N'-Dihydroxypyromellitimide (CAS No. 57583-53-6) represents a compelling subject of study due to its structural versatility and biological relevance. Its potential applications span multiple therapeutic areas, driven by ongoing research efforts aimed at elucidating its mechanisms and optimizing its pharmacological profile. As advancements continue to emerge from both synthetic chemistry and biomedical research,N,N'-Dihydroxypyromellitimide is poised to play an increasingly important role in addressing complex diseases through innovative drug design strategies.

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