Cas no 5876-91-5 (2-(Methoxymethoxy)benzoic Acid)

2-(Methoxymethoxy)benzoic Acid is a versatile benzoic acid derivative featuring a methoxymethoxy functional group at the ortho position. This compound is primarily utilized as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. The methoxymethoxy group enhances its reactivity, making it valuable for protecting group strategies or further functionalization. Its stability under various reaction conditions and compatibility with common synthetic methodologies contribute to its utility in multi-step synthesis. The compound is typically supplied in high purity, ensuring consistent performance in research and industrial applications. Proper handling and storage under inert conditions are recommended to maintain its integrity.
2-(Methoxymethoxy)benzoic Acid structure
5876-91-5 structure
Product Name:2-(Methoxymethoxy)benzoic Acid
CAS No:5876-91-5
MF:C9H10O4
MW:182.173303127289
CID:340943
PubChem ID:10856115
Update Time:2025-05-23

2-(Methoxymethoxy)benzoic Acid Chemical and Physical Properties

Names and Identifiers

    • 2-(Methoxymethoxy)benzoic Acid
    • 2-(Methoxymethoxy)be
    • 2-(METHOXYMETHOXY)BENZOIC ACID,WHITE SOLID
    • Benzoic acid, 2-(methoxymethoxy)-
    • 2-(methoxymethoxy)benzoate
    • 2-(methoxymethyloxy)benzoic acid
    • 2-Methoxymethoxy-benzoesaeure
    • 2-methoxymethoxy-benzoic acid
    • 2-methoxymethyloxybenzoic acid
    • 2-MOM salicylic acid
    • CTK1E8935
    • FT-0671248
    • KB-224137
    • Methoxymethylaethersalicylsaeure
    • o-(Methoxymethoxy)benzoic Acid
    • SureCN2290756
    • AKOS009075902
    • 5876-91-5
    • ARNVPLFYBZBHPU-UHFFFAOYSA-N
    • SCHEMBL2290756
    • 2-methoxymethoxybenzoic acid
    • DTXSID10446016
    • Benzoic acid, 2-(methoxymethoxy)-; Benzoic acid, o-(methoxymethoxy)- (7CI,8CI); 2-(Methoxymethoxy)benzoic acid; 2-(Methoxymethyloxy)benzoic acid; O-(Methoxymethyl)salicylic acid; Salicylic acid methoxymethyl ether
    • DB-291985
    • Inchi: 1S/C9H10O4/c1-12-6-13-8-5-3-2-4-7(8)9(10)11/h2-5H,6H2,1H3,(H,10,11)
    • InChI Key: ARNVPLFYBZBHPU-UHFFFAOYSA-N
    • SMILES: O(COC)C1C=CC=CC=1C(=O)O

Computed Properties

  • Exact Mass: 182.0579
  • Monoisotopic Mass: 182.05790880g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 4
  • Complexity: 169
  • 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: 1.5
  • Topological Polar Surface Area: 55.8?2

Experimental Properties

  • PSA: 55.76

2-(Methoxymethoxy)benzoic Acid Pricemore >>

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2-(Methoxymethoxy)benzoic Acid Related Literature

Additional information on 2-(Methoxymethoxy)benzoic Acid

2-(Methoxymethoxy)benzoic Acid: A Comprehensive Overview

2-(Methoxymethoxy)benzoic acid, also known by its CAS registry number CAS No. 5876-91-5, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound, characterized by its unique structure, has garnered attention due to its potential applications in drug development and material science. Recent studies have highlighted its role in various biochemical pathways, making it a subject of intensive research.

The molecular structure of 2-(Methoxymethoxy)benzoic acid comprises a benzoic acid moiety with a methoxymethoxy substituent at the para position. This substitution pattern imparts distinct chemical properties, including enhanced solubility and stability under certain conditions. Researchers have explored its synthesis through various routes, including nucleophilic aromatic substitution and coupling reactions, which have been optimized to achieve high yields and purity.

Recent advancements in computational chemistry have enabled detailed modeling of the compound's interactions with biological systems. For instance, molecular docking studies have revealed potential binding affinities with key enzymes involved in inflammatory pathways, suggesting its potential as an anti-inflammatory agent. Furthermore, spectroscopic analyses, such as NMR and IR spectroscopy, have provided insights into its conformational flexibility and electronic properties.

In terms of applications, 2-(Methoxymethoxy)benzoic acid has shown promise in the development of novel pharmaceuticals. Its ability to modulate cellular signaling pathways makes it a candidate for treating conditions such as neurodegenerative diseases and cancer. Additionally, its incorporation into polymer matrices has been investigated for use in advanced materials with tailored mechanical and thermal properties.

Environmental impact assessments have also been conducted to evaluate the compound's biodegradability and toxicity. Studies indicate that under aerobic conditions, the compound undergoes efficient microbial degradation, reducing its environmental footprint. However, further research is required to fully understand its long-term effects on ecosystems.

In conclusion, 2-(Methoxymethoxy)benzoic acid represents a versatile compound with diverse applications across multiple disciplines. Its chemical properties, synthesis methods, and biological activities continue to be explored through cutting-edge research methodologies. As our understanding of this compound deepens, it holds the potential to contribute significantly to both therapeutic development and material innovation.

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