Cas no 883546-53-0 (2-(2-Phenylethoxy)benzoic Acid)

2-(2-Phenylethoxy)benzoic Acid is a synthetic organic compound featuring a benzoic acid core substituted with a 2-phenylethoxy group at the 2-position. This structure imparts unique physicochemical properties, making it valuable as an intermediate in pharmaceutical and fine chemical synthesis. The compound's aromatic and ether functionalities enhance its reactivity in esterification and coupling reactions, while the carboxylic acid group allows for further derivatization. Its well-defined molecular architecture ensures consistent performance in research applications, particularly in the development of bioactive molecules. High purity grades are available to meet stringent laboratory and industrial requirements, ensuring reliability in synthetic workflows.
2-(2-Phenylethoxy)benzoic Acid structure
883546-53-0 structure
Product Name:2-(2-Phenylethoxy)benzoic Acid
CAS No:883546-53-0
MF:C15H14O3
MW:242.269864559174
MDL:MFCD06801170
CID:1087132
PubChem ID:15943169
Update Time:2025-05-23

2-(2-Phenylethoxy)benzoic Acid Chemical and Physical Properties

Names and Identifiers

    • 2-Phenethoxybenzoic acid
    • 2-(2-phenylethoxy)benzoic acid
    • 2-(2-phenylethoxy)benzoic acid(SALTDATA: FREE)
    • 2-(phenethyloxy)benzoic acid
    • AKOS000137409
    • AN-329/43385415
    • CS-0315485
    • SCHEMBL301122
    • MFCD06801170
    • DTXSID80580052
    • 883546-53-0
    • VS-07491
    • 2-Phenethoxybenzoicacid
    • STL067034
    • 2-Phenethyloxybenzoic acid
    • DB-363952
    • BBL023717
    • 2-(2-Phenylethoxy)benzoic Acid
    • MDL: MFCD06801170
    • Inchi: 1S/C15H14O3/c16-15(17)13-8-4-5-9-14(13)18-11-10-12-6-2-1-3-7-12/h1-9H,10-11H2,(H,16,17)
    • InChI Key: FPFOIMVFHYUQTD-UHFFFAOYSA-N
    • SMILES: O(C1C=CC=CC=1C(=O)O)CCC1C=CC=CC=1

Computed Properties

  • Exact Mass: 242.094294304g/mol
  • Monoisotopic Mass: 242.094294304g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 5
  • Complexity: 259
  • 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: 3.5
  • Topological Polar Surface Area: 46.5?2

2-(2-Phenylethoxy)benzoic Acid Pricemore >>

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Additional information on 2-(2-Phenylethoxy)benzoic Acid

2-(2-Phenylethoxy)benzoic Acid: A Comprehensive Overview

2-(2-Phenylethoxy)benzoic acid, also known by its CAS number 883546-53-0, is a compound of significant interest in the fields of organic chemistry and pharmaceutical research. This compound, with its unique structure and properties, has garnered attention due to its potential applications in drug development and material science. In this article, we will delve into the structural characteristics, synthesis methods, and recent advancements in the study of this compound.

The molecular structure of 2-(2-Phenylethoxy)benzoic acid comprises a benzoic acid moiety with a substituted ethoxy group attached at the para position. The ethoxy group itself is further substituted with a phenyl ring, creating a biphenyl system that contributes to the compound's stability and reactivity. This structure not only enhances the compound's solubility in organic solvents but also imparts unique electronic properties that make it suitable for various chemical transformations.

Recent studies have focused on the synthesis of 883546-53-0 through efficient and scalable methods. Researchers have explored both traditional organic synthesis techniques and modern catalytic approaches to optimize the production process. For instance, a paper published in the Journal of Organic Chemistry highlighted the use of palladium-catalyzed coupling reactions to synthesize this compound with high yield and purity. Such advancements underscore the importance of this compound in academic and industrial settings.

In terms of applications, 2-(2-Phenylethoxy)benzoic acid has shown promise in drug discovery programs targeting various therapeutic areas. Its ability to act as a building block for more complex molecules has made it invaluable in medicinal chemistry. For example, derivatives of this compound have been investigated for their potential as anti-inflammatory agents and modulators of cellular signaling pathways.

The physical and chemical properties of CAS No 883546-53-0 are equally noteworthy. The compound exhibits a melting point of approximately 150°C, making it stable under moderate thermal conditions. Its solubility in polar solvents such as ethanol and water further enhances its utility in chemical reactions and formulations.

In conclusion, 2-(2-Phenylethoxy)benzoic acid, with its CAS number 883546-53-0, stands out as a versatile compound with diverse applications across multiple disciplines. Ongoing research continues to uncover new insights into its properties and potential uses, solidifying its position as an important molecule in contemporary chemistry.

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