Cas no 1261913-83-0 (4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid)

4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid is a substituted benzoic acid derivative with potential applications in pharmaceutical and agrochemical research. Its molecular structure, featuring chloro, ethoxy, and methoxy functional groups, offers versatility in synthetic pathways, making it a valuable intermediate for developing bioactive compounds. The compound exhibits moderate solubility in organic solvents, facilitating its use in various reaction conditions. Its well-defined crystalline form ensures consistent purity and stability, which is critical for precise experimental outcomes. Researchers may explore its utility in designing enzyme inhibitors or herbicides due to its aromatic substitution pattern. Proper handling and storage under inert conditions are recommended to maintain its integrity.
4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid structure
1261913-83-0 structure
Product Name:4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid
CAS No:1261913-83-0
MF:C16H15ClO4
MW:306.740904092789
MDL:MFCD18322326
CID:2763105
PubChem ID:53228157
Update Time:2025-08-05

4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid Chemical and Physical Properties

Names and Identifiers

    • 2'-Chloro-4'-ethoxy-3-methoxy[1,1'-biphenyl]-4-carboxylic acid
    • 4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid, 95%
    • DTXSID60691690
    • 1261913-83-0
    • 4-(2-CHLORO-4-ETHOXYPHENYL)-2-METHOXYBENZOIC ACID
    • MFCD18322326
    • 4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid
    • MDL： MFCD18322326
    • Inchi： 1S/C16H15ClO4/c1-3-21-11-5-7-12(14(17)9-11)10-4-6-13(16(18)19)15(8-10)20-2/h4-9H,3H2,1-2H3,(H,18,19)
    • InChI Key： TZGVSKNZKUTJJY-UHFFFAOYSA-N
    • SMILES： ClC1C=C(C=CC=1C1C=CC(C(=O)O)=C(C=1)OC)OCC

Computed Properties

  • Exact Mass: 306.0658866Da
  • Monoisotopic Mass: 306.0658866Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 5
  • Complexity: 349
  • 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: 55.8?2

4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB329602-5 g
4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid, 95%; .
 1261913-83-0 95%
5g
 €1159.00 2023-04-26
abcr
AB329602-5g
4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid, 95%; .
 1261913-83-0 95%
5g
 €1159.00 2025-04-21

4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid Related Literature

Additional information on 4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid

Comprehensive Overview of 4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid (CAS No. 1261913-83-0)

4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid (CAS No. 1261913-83-0) is a specialized organic compound with a molecular formula of C16H15ClO4. This compound belongs to the class of substituted benzoic acids, which are widely studied for their potential applications in pharmaceuticals, agrochemicals, and material science. The presence of both chloro and ethoxy functional groups in its structure makes it a versatile intermediate for further chemical modifications. Researchers and industries are increasingly interested in this compound due to its unique physicochemical properties and potential role in drug discovery.

One of the key features of 4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid is its structural complexity, which allows it to interact with various biological targets. The methoxybenzoic acid moiety is particularly noteworthy, as it is often associated with anti-inflammatory and antimicrobial activities. This has led to a surge in searches for "benzoic acid derivatives in drug development" and "chloro-substituted phenyl compounds," reflecting the growing interest in this niche. The compound's CAS No. 1261913-83-0 is frequently queried in scientific databases, underscoring its relevance in current research.

From a synthetic chemistry perspective, 4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid serves as a valuable building block. Its ethoxy and chloro substituents enable selective reactions, making it a preferred choice for constructing more complex molecules. Recent trends in organic synthesis highlight the demand for "high-purity benzoic acid intermediates" and "customized aromatic compounds," aligning with the compound's utility. Additionally, its stability under various conditions makes it suitable for scalable production, a topic often explored in industrial chemistry forums.

Environmental and regulatory considerations are also critical when discussing 4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid. With increasing emphasis on "green chemistry" and "sustainable synthesis," researchers are evaluating eco-friendly methods to produce such compounds. The compound's biodegradability and toxicity profile are subjects of ongoing studies, addressing common queries like "environmental impact of chloro-aromatics." These discussions are vital for ensuring compliance with global safety standards while maintaining innovation in chemical design.

In conclusion, 4-(2-Chloro-4-ethoxyphenyl)-2-methoxybenzoic acid (CAS No. 1261913-83-0) represents a fascinating intersection of chemistry and applied science. Its structural attributes, combined with emerging trends in drug discovery and sustainable chemistry, position it as a compound of significant interest. As the scientific community continues to explore its potential, this molecule is likely to remain a focal point in both academic and industrial research.

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