Cas no 58841-72-8 (Dibenzofuran-2-carboxylic acid methyl ester)

Dibenzofuran-2-carboxylic acid methyl ester is a high-purity organic compound with the molecular formula C??H??O?. It serves as a versatile intermediate in pharmaceutical and agrochemical synthesis, particularly in the development of heterocyclic compounds. The ester functional group enhances its reactivity, making it suitable for further derivatization. Its dibenzofuran core provides structural stability and potential for π-π stacking interactions, which can be advantageous in material science applications. The compound is typically characterized by its crystalline solid form and moderate solubility in common organic solvents. Its well-defined structure and consistent purity make it a reliable choice for research and industrial applications requiring precise chemical building blocks.
Dibenzofuran-2-carboxylic acid methyl ester structure
58841-72-8 structure
Product Name:Dibenzofuran-2-carboxylic acid methyl ester
CAS No:58841-72-8
MF:C14H10O3
MW:226.227404117584
CID:3150640
PubChem ID:3702628
Update Time:2025-05-21

Dibenzofuran-2-carboxylic acid methyl ester Chemical and Physical Properties

Names and Identifiers

    • Dibenzofuran-2-carboxylic acid methyl ester
    • 2-Dibenzofurancarboxylic acid, methyl ester
    • methyl dibenzo[b,d]furan-2-carboxylate
    • 58841-72-8
    • SCHEMBL8954225
    • AKOS003348518
    • DB-377324
    • methyldibenzo[b,d]furan-2-carboxylate
    • Methyl Dibenzofuran-2-carboxylate
    • MDL: MFCD00094106
    • Inchi: 1S/C14H10O3/c1-16-14(15)9-6-7-13-11(8-9)10-4-2-3-5-12(10)17-13/h2-8H,1H3
    • InChI Key: QSQTUIVYNKZDHU-UHFFFAOYSA-N
    • SMILES: O1C2C=CC=CC=2C2C=C(C(=O)OC)C=CC1=2

Computed Properties

  • Exact Mass: 226.062994177g/mol
  • Monoisotopic Mass: 226.062994177g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 2
  • Complexity: 302
  • 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: 4
  • Topological Polar Surface Area: 39.4?2

Dibenzofuran-2-carboxylic acid methyl ester Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1536583-1g
Methyl dibenzo[b,d]furan-2-carboxylate
58841-72-8 98%
1g
¥5663.00 2024-05-07

Additional information on Dibenzofuran-2-carboxylic acid methyl ester

Comprehensive Overview of Dibenzofuran-2-carboxylic acid methyl ester (CAS No. 58841-72-8)

Dibenzofuran-2-carboxylic acid methyl ester (CAS No. 58841-72-8) is a specialized organic compound widely utilized in pharmaceutical research, material science, and fine chemical synthesis. This ester derivative of dibenzofuran is gaining attention due to its unique structural properties, which make it a valuable intermediate in the development of advanced materials and bioactive molecules. Researchers and industries are increasingly exploring its potential in green chemistry applications, aligning with the global shift toward sustainable and eco-friendly processes.

The compound's molecular structure, featuring a dibenzofuran core with a methyl ester functional group, offers versatility in synthetic pathways. Its CAS No. 58841-72-8 serves as a critical identifier in chemical databases, ensuring accurate referencing in academic and industrial settings. Recent studies highlight its role in the synthesis of fluorescent dyes and organic electronic materials, addressing the growing demand for high-performance optoelectronic devices. This aligns with trending searches for "organic semiconductors" and "sustainable material alternatives," reflecting broader market interests.

In pharmaceutical applications, Dibenzofuran-2-carboxylic acid methyl ester is investigated for its potential as a scaffold in drug discovery. Its rigid aromatic system and modifiable ester group enable the design of novel therapeutic agents, particularly in oncology and neurology. Online queries such as "dibenzofuran derivatives in medicine" and "ester-based drug intermediates" underscore the compound's relevance in cutting-edge research. Additionally, its stability under various conditions makes it a preferred choice for high-throughput screening and combinatorial chemistry.

From an industrial perspective, the compound's synthesis and purification methods are optimized for scalability, catering to the needs of fine chemical manufacturers. Innovations in catalytic esterification and solvent-free reactions have further enhanced its production efficiency, reducing environmental impact. These advancements resonate with search trends like "green synthesis of esters" and "cost-effective chemical processes," demonstrating the intersection of science and sustainability.

Quality control and analytical characterization of Dibenzofuran-2-carboxylic acid methyl ester rely on advanced techniques such as HPLC, GC-MS, and NMR spectroscopy. These methods ensure compliance with regulatory standards and meet the demands of high-purity applications. Frequently searched terms like "analytical methods for esters" and "purity testing of dibenzofuran compounds" reflect the importance of rigorous quality assurance in the chemical industry.

In summary, Dibenzofuran-2-carboxylic acid methyl ester (CAS No. 58841-72-8) represents a multifaceted compound with significant applications across diverse fields. Its integration into sustainable technologies, pharmaceutical innovation, and material science positions it as a compound of enduring interest. As research continues to uncover new possibilities, its role in addressing contemporary scientific challenges will likely expand, further solidifying its importance in modern chemistry.

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