Cas no 1261981-31-0 (5-methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid)

5-Methoxy-2-(3-phenylmethoxyphenyl)benzoic acid is a synthetic benzoic acid derivative characterized by its methoxy and phenylmethoxy substituents, which confer unique chemical properties. This compound is of interest in pharmaceutical and organic synthesis due to its potential as an intermediate in the development of bioactive molecules. Its aromatic structure and functional groups make it suitable for further derivatization, enabling applications in medicinal chemistry research. The presence of both electron-donating methoxy and phenylmethoxy groups enhances its reactivity in electrophilic substitution reactions. This compound is typically handled under controlled conditions due to its sensitivity to light and moisture, ensuring stability during storage and use. Its purity and structural specificity make it valuable for precise synthetic applications.
5-methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid structure
1261981-31-0 structure
Product Name:5-methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid
CAS No:1261981-31-0
MF:C21H18O4
MW:334.365226268768
MDL:MFCD18322876
CID:1219425
PubChem ID:53228697
Update Time:2025-05-21

5-methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid Chemical and Physical Properties

Names and Identifiers

    • 5-methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid
    • MFCD18322876
    • DTXSID30692230
    • 3'-(Benzyloxy)-4-methoxy[1,1'-biphenyl]-2-carboxylic acid
    • 2-(3-BENZYLOXYPHENYL)-5-METHOXYBENZOIC ACID
    • 1261981-31-0
    • 2-(3-Benzyloxyphenyl)-5-methoxybenzoic acid, 95%
    • MDL: MFCD18322876
    • Inchi: 1S/C21H18O4/c1-24-17-10-11-19(20(13-17)21(22)23)16-8-5-9-18(12-16)25-14-15-6-3-2-4-7-15/h2-13H,14H2,1H3,(H,22,23)
    • InChI Key: NTLVLKXOVOBYQB-UHFFFAOYSA-N
    • SMILES: O(CC1C=CC=CC=1)C1=CC=CC(=C1)C1C=CC(=CC=1C(=O)O)OC

Computed Properties

  • Exact Mass: 334.12050905g/mol
  • Monoisotopic Mass: 334.12050905g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 25
  • Rotatable Bond Count: 6
  • Complexity: 418
  • 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: 4.5
  • Topological Polar Surface Area: 55.8?2

5-methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB330155-5 g
2-(3-Benzyloxyphenyl)-5-methoxybenzoic acid, 95%; .
1261981-31-0 95%
5g
€1159.00 2023-04-26
abcr
AB330155-5g
2-(3-Benzyloxyphenyl)-5-methoxybenzoic acid, 95%; .
1261981-31-0 95%
5g
€1159.00 2025-04-21

Additional information on 5-methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid

Comprehensive Guide to 5-Methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid (CAS No. 1261981-31-0)

5-Methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid (CAS No. 1261981-31-0) is a specialized organic compound with a unique molecular structure that combines methoxy, phenylmethoxy, and benzoic acid functional groups. This compound has garnered significant attention in pharmaceutical and materials science research due to its versatile properties and potential applications. The CAS number 1261981-31-0 serves as a unique identifier for this chemical, ensuring precise identification in global databases.

The molecular structure of 5-Methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid features a central benzoic acid core substituted with a methoxy group at the 5-position and a phenylmethoxy group at the 2-position. This arrangement contributes to its distinct chemical behavior, including solubility in organic solvents and moderate stability under standard conditions. Researchers often explore its synthetic pathways and derivatization potential, making it a subject of interest in medicinal chemistry.

One of the most discussed applications of CAS 1261981-31-0 is its role as an intermediate in the synthesis of bioactive molecules. Recent studies highlight its utility in developing anti-inflammatory agents and enzyme inhibitors, aligning with the growing demand for novel therapeutic compounds. The compound's ability to modulate biological pathways has positioned it as a candidate for further investigation in drug discovery programs.

In the context of materials science, 5-Methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid has been explored for its potential in creating advanced polymers and coatings. Its aromatic structure and functional groups enable interactions with other monomers, facilitating the design of materials with tailored properties. This aligns with current trends in sustainable materials and green chemistry, where researchers seek eco-friendly alternatives to conventional synthetic methods.

The market for CAS 1261981-31-0 is influenced by its niche applications and the expanding pharmaceutical industry. Suppliers and manufacturers emphasize high-purity grades to meet the stringent requirements of research and development. Analytical techniques such as HPLC and NMR spectroscopy are commonly employed to verify the compound's purity and structural integrity, ensuring reproducibility in experimental settings.

From an SEO perspective, queries related to "5-Methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid synthesis" and "CAS 1261981-31-0 applications" reflect user interest in its practical uses. Additionally, searches for "buy 5-Methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid" indicate commercial demand, underscoring the importance of detailed product information for potential buyers. Addressing these topics enhances the article's relevance and visibility in search engine results.

Safety and handling of 5-Methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid are critical considerations for laboratory personnel. While not classified as hazardous, standard precautions for handling organic compounds—such as using personal protective equipment (PPE) and working in well-ventilated areas—are recommended. Proper storage conditions, including protection from light and moisture, help maintain the compound's stability over time.

Future research directions for CAS 1261981-31-0 may focus on optimizing its synthetic routes to improve yield and scalability. Collaborative efforts between academia and industry could unlock new applications, particularly in targeted drug delivery systems and functional materials. As scientific advancements continue, this compound is poised to play a pivotal role in interdisciplinary innovations.

In summary, 5-Methoxy-2-(3-phenylmethoxyphenyl)benzoic Acid (CAS No. 1261981-31-0) represents a valuable chemical entity with broad research and industrial potential. Its structural complexity and functional versatility make it a subject of ongoing exploration, driven by the evolving needs of modern science and technology.

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