Cas no 2026-27-9 (1,1'-Biphenyl,3,3',4,4'-tetramethoxy-)

1,1'-Biphenyl,3,3',4,4'-tetramethoxy- is a tetramethoxy-substituted biphenyl compound characterized by its symmetrical aromatic structure. This derivative is notable for its high purity and stability, making it suitable for applications in organic synthesis, particularly as an intermediate in the production of advanced materials and pharmaceuticals. The methoxy groups enhance its solubility in organic solvents, facilitating its use in cross-coupling reactions and other synthetic transformations. Its well-defined molecular structure ensures consistent performance in research and industrial processes. The compound is typically supplied with rigorous quality control to meet the demands of specialized chemical applications, ensuring reliability in experimental and production settings.
1,1'-Biphenyl,3,3',4,4'-tetramethoxy- structure
2026-27-9 structure
Product Name:1,1'-Biphenyl,3,3',4,4'-tetramethoxy-
CAS No:2026-27-9
MF:C16H18O4
MW:274.311725139618
CID:270958
PubChem ID:266846
Update Time:2025-10-19

1,1'-Biphenyl,3,3',4,4'-tetramethoxy- Chemical and Physical Properties

Names and Identifiers

    • 1,1'-Biphenyl,3,3',4,4'-tetramethoxy-
    • 3,3',4,4'-TETRAMETHOXY-1,1'-BIPHENYL
    • 4-(3,4-dimethoxyphenyl)-1,2-dimethoxybenzene
    • 3,3',4,4'-tetramethoxybiphenyl
    • 3,3',4,4'-tetramethoxylbiphenyl
    • 3,4,3',4'-Tetramethoxy-biphenyl
    • 3.4.3'.4'-Tetramethoxy-diphenyl
    • AC1L6GXX
    • CTK4E3691
    • NCIOpen2_007274
    • NSC105649
    • SureCN8840880
    • ZADYUYOJVLZYAQ-UHFFFAOYSA-N
    • 3,3',4,4'-Tetramethoxydiphenyl
    • 4-(3, 4-dimethoxyphenyl)-1, 2-dimethoxybenzene
    • AKOS000277058
    • NSC-105649
    • SCHEMBL8840880
    • 4-(3,4-dimethoxyphenyl)-1,2-dimethoxy-benzene
    • 2026-27-9
    • DTXSID30295826
    • 1,1'-biphenyl, 3,3',4,4'-tetramethoxy-
    • 3,4,3',4'-Tetramethoxy diphenyl
    • Inchi: 1S/C16H18O4/c1-17-13-7-5-11(9-15(13)19-3)12-6-8-14(18-2)16(10-12)20-4/h5-10H,1-4H3
    • InChI Key: ZADYUYOJVLZYAQ-UHFFFAOYSA-N
    • SMILES: O(C)C1=C(C=CC(=C1)C1C=CC(=C(C=1)OC)OC)OC

Computed Properties

  • Exact Mass: 274.12054
  • Monoisotopic Mass: 274.120509
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 5
  • Complexity: 256
  • 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
  • Topological Polar Surface Area: 36.9
  • XLogP3: 3.4

Experimental Properties

  • Density: 1.094
  • Boiling Point: 372.9°Cat760mmHg
  • Flash Point: 123°C
  • Refractive Index: 1.53
  • PSA: 36.92
  • LogP: 3.38800

1,1'-Biphenyl,3,3',4,4'-tetramethoxy- Pricemore >>

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1,1'-Biphenyl,3,3',4,4'-tetramethoxy- Related Literature

Additional information on 1,1'-Biphenyl,3,3',4,4'-tetramethoxy-

1,1'-Biphenyl,3,3',4,4'-tetramethoxy (CAS No. 2026-27-9)

The compound 1,1'-biphenyl,3,3',4,4'-tetramethoxy (CAS No. 2026-27-9) is a highly specialized organic molecule with a unique structure and diverse applications in various scientific and industrial fields. This compound is characterized by its biphenyl core structure with four methoxy groups attached at the 3, 3', 4, and 4' positions of the benzene rings. The presence of these methoxy groups imparts specific electronic and steric properties to the molecule, making it valuable in research and development.

Structure and Properties: The molecular structure of 1,1'-biphenyl,3,3',4,4'-tetramethoxy consists of two benzene rings connected by a single bond (biphenyl system). The methoxy groups (-OCH?) are electron-donating substituents that activate the aromatic rings toward electrophilic substitution reactions. This electronic activation makes the compound useful in various synthetic pathways where controlled reactivity is desired.

Synthesis and Applications: The synthesis of 1,1'-biphenyl derivatives has been extensively studied due to their potential in materials science and pharmaceuticals. Recent research has focused on using this compound as a precursor for synthesizing advanced materials such as organic semiconductors and optoelectronic devices. For instance, studies have shown that derivatives of 1,1'-biphenyl systems can be used to create efficient OLEDs (Organic Light Emitting Diodes) with improved luminous efficiency and stability.

Pharmacological Applications: In the field of pharmacology, 1,1'-biphenyl derivatives have been explored for their potential as drug candidates. Recent findings indicate that certain analogs of this compound exhibit anti-tumor activity by targeting specific signaling pathways in cancer cells. These studies highlight the importance of understanding the structure-activity relationships in biphenyl-based compounds for drug discovery.

Environmental Considerations: While 1,1'-biphenyl compounds are valuable in various applications, their environmental impact remains a critical area of study. Research into the biodegradation and toxicity profiles of these compounds is ongoing to ensure their safe use in industrial processes.

In conclusion, 1,1'-biphenyl derivatives, particularly those with multiple methoxy substituents like 1,1'-biphenyl-3-carboxylic acid, continue to be a focal point in scientific research due to their versatile properties and wide-ranging applications.

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