Cas no 1269448-82-9 (Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate)

Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate is a versatile intermediate in organic synthesis, particularly valued for its bifunctional ester and amino groups, which enable diverse chemical modifications. The compound’s aromatic ether linkage and ester functionalities contribute to its stability while allowing selective reactivity under controlled conditions. Its structural features make it suitable for applications in pharmaceutical and agrochemical research, where it serves as a precursor for heterocyclic compounds or active ingredient synthesis. The presence of both electron-donating (amino) and electron-withdrawing (ester) groups enhances its utility in fine-tuning electronic properties in target molecules. High purity grades ensure consistent performance in synthetic workflows.
Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate structure
1269448-82-9 structure
Product Name:Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate
CAS No:1269448-82-9
MF:C16H15NO5
MW:301.294004678726
MDL:MFCD17015023
CID:1033247
PubChem ID:66524782
Update Time:2025-06-14

Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate Chemical and Physical Properties

Names and Identifiers

    • Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate
    • 5-amino-2-[2-(methoxycarbonyl)phenoxy]Benzoic acid methyl ester
    • 5-Amino-2-(2-methoxycarbonyl-phenoxy)-benzoic acid methyl ester
    • AK119662
    • KB-257363
    • MolPort-020-014-119
    • QC-1751
    • Methyl5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate
    • MFCD17015023
    • SB82993
    • A889321
    • methyl 5-amino-2-(2-methoxycarbonylphenoxy)benzoate
    • DB-050611
    • DTXSID10735139
    • AKOS015968944
    • F71451
    • AC-27702
    • 1269448-82-9
    • Benzoic acid, 5-amino-2-[2-(methoxycarbonyl)phenoxy]-, methyl ester
    • Methyl 5-amino-2-[2-(methoxycarbonyl)phenoxy]benzoate
    • MDL: MFCD17015023
    • Inchi: 1S/C16H15NO5/c1-20-15(18)11-5-3-4-6-13(11)22-14-8-7-10(17)9-12(14)16(19)21-2/h3-9H,17H2,1-2H3
    • InChI Key: RLWRZAZMFRUEIM-UHFFFAOYSA-N
    • SMILES: O(C1C=CC=CC=1C(=O)OC)C1C=CC(=CC=1C(=O)OC)N

Computed Properties

  • Exact Mass: 301.09502258g/mol
  • Monoisotopic Mass: 301.09502258g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 22
  • Rotatable Bond Count: 6
  • Complexity: 400
  • 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: 2.5
  • Topological Polar Surface Area: 87.8?2

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Additional information on Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate

Comprehensive Overview of Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate (CAS No. 1269448-82-9)

Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate (CAS No. 1269448-82-9) is a specialized organic compound that has garnered significant attention in pharmaceutical and chemical research. This ester derivative is characterized by its unique molecular structure, which includes both amino and methoxycarbonyl functional groups. These features make it a valuable intermediate in the synthesis of more complex molecules, particularly in the development of drug candidates and biologically active compounds.

The compound's CAS number 1269448-82-9 serves as a unique identifier, ensuring precise referencing in scientific literature and regulatory documents. Researchers often search for "Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate uses" or "CAS 1269448-82-9 applications" to explore its potential in various fields. Its versatility stems from its ability to participate in esterification and amination reactions, which are critical in organic synthesis.

In recent years, the demand for high-purity chemical intermediates like Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate has surged, driven by advancements in medicinal chemistry and drug discovery. The compound's role in the synthesis of targeted therapies and small-molecule inhibitors has made it a subject of interest for researchers investigating cancer treatment and inflammatory diseases. These applications align with current trends in personalized medicine and precision healthcare.

From a technical perspective, the synthesis of Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate involves multi-step organic reactions, often requiring catalysts and controlled conditions to achieve optimal yields. Questions like "How to synthesize Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate?" or "CAS 1269448-82-9 synthesis protocol" are frequently encountered in academic and industrial research forums. The compound's stability and solubility properties also make it suitable for various formulation studies.

Another area of interest is the compound's potential in green chemistry initiatives. Researchers are exploring eco-friendly synthesis routes for Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate to minimize environmental impact. This aligns with global efforts to promote sustainable chemical production and reduce carbon footprints. Searches related to "sustainable synthesis of CAS 1269448-82-9" reflect this growing trend.

In summary, Methyl 5-amino-2-(2-(methoxycarbonyl)phenoxy)benzoate (CAS No. 1269448-82-9) is a multifaceted compound with broad applications in pharmaceutical research, organic synthesis, and sustainable chemistry. Its unique structural attributes and functional groups make it a valuable asset for scientists and industries alike. As research continues to evolve, this compound is likely to play an even more prominent role in addressing contemporary challenges in healthcare and environmental sustainability.

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