Cas no 193903-62-7 (Benzaldehyde,4,4'-(2,5-thiophenediyl)bis- (9CI))

Benzaldehyde,4,4'-(2,5-thiophenediyl)bis- (9CI) is a bifunctional aromatic aldehyde featuring a central thiophene ring linked to two benzaldehyde groups. This compound is of interest in organic synthesis and materials science due to its rigid, conjugated structure, which enhances electronic properties and stability. The presence of reactive aldehyde groups allows for further functionalization, making it a versatile intermediate in the preparation of polymers, ligands, and heterocyclic compounds. Its thiophene core contributes to potential applications in optoelectronic materials, such as organic semiconductors or photovoltaic devices. The compound's well-defined symmetry and high purity also facilitate controlled polymerization and precise molecular design.
Benzaldehyde,4,4'-(2,5-thiophenediyl)bis- (9CI) structure
193903-62-7 structure
Product Name:Benzaldehyde,4,4'-(2,5-thiophenediyl)bis- (9CI)
CAS No:193903-62-7
MF:C18H12O2S
MW:292.351683616638
CID:116486
PubChem ID:53422924
Update Time:2025-09-28

Benzaldehyde,4,4'-(2,5-thiophenediyl)bis- (9CI) Chemical and Physical Properties

Names and Identifiers

    • Benzaldehyde,4,4'-(2,5-thiophenediyl)bis- (9CI)
    • 2,5-DI(4-FORMYLPHENYL)THIOPHENE
    • 4-[5-(4-formylphenyl)thiophen-2-yl]benzaldehyde
    • 2,5-bis[4-(formyl)phenyl]thiophene
    • 2,5-Diphenylthiophene-4',4"-dialdehyde
    • 4,4'-thiene-2,5-diyldibenzaldehyde
    • 4,4'-(Thiophene-2,5-diyl)dibenzaldehyde
    • 4,4'-(Thiene-2,5-diyl)dibenzaldehyde
    • YSZC1301
    • CS-0170125
    • 4,4-(thiophene-2,5-diyl)dibenzaldehyde
    • DTXSID60698184
    • 193903-62-7
    • G63924
    • Inchi: 1S/C18H12O2S/c19-11-13-1-5-15(6-2-13)17-9-10-18(21-17)16-7-3-14(12-20)4-8-16/h1-12H
    • InChI Key: VORIIBWJNVKTPM-UHFFFAOYSA-N
    • SMILES: S1C(=CC=C1C1C=CC(C=O)=CC=1)C1C=CC(C=O)=CC=1

Computed Properties

  • Exact Mass: 292.05600
  • Monoisotopic Mass: 292.056
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 4
  • Complexity: 320
  • 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
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 3.9
  • Topological Polar Surface Area: 62.4A^2

Experimental Properties

  • PSA: 62.38000
  • LogP: 4.70710

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Additional information on Benzaldehyde,4,4'-(2,5-thiophenediyl)bis- (9CI)

Introduction to Benzaldehyde,4,4'-(2,5-thiophenediyl)bis-(9CI) and Its Significance in Modern Chemical Research

Benzaldehyde,4,4'-(2,5-thiophenediyl)bis-(9CI) is a compound with the CAS number 193903-62-7, which has garnered significant attention in the field of chemical and pharmaceutical research. This compound, characterized by its unique structural and chemical properties, plays a pivotal role in various applications ranging from material science to drug development. The presence of a 2,5-thiophenediyl bridge in its molecular structure imparts distinct reactivity and functionality, making it a valuable candidate for synthetic chemistry and molecular design.

The study of Benzaldehyde,4,4'-(2,5-thiophenediyl)bis-(9CI) has been extensively explored in recent years, particularly in the context of its potential applications in pharmaceuticals. Researchers have been investigating its role as an intermediate in the synthesis of complex organic molecules, including those with therapeutic properties. The compound's ability to undergo various chemical transformations makes it a versatile building block for the development of novel drugs and agrochemicals.

In the realm of material science, Benzaldehyde,4,4'-(2,5-thiophenediyl)bis-(9CI) has been utilized in the creation of advanced materials with tailored electronic and optical properties. The incorporation of the 2,5-thiophenediyl moiety into polymers and organic semiconductors has led to the development of materials with enhanced performance characteristics. These materials are particularly relevant in the fabrication of organic light-emitting diodes (OLEDs), solar cells, and other optoelectronic devices.

The pharmacological potential of Benzaldehyde,4,4'-(2,5-thiophenediyl)bis-(9CI) has also been a subject of intense research. Studies have shown that derivatives of this compound exhibit promising biological activities, including anti-inflammatory and antioxidant properties. The structural motif of the 2,5-thiophenediyl bridge is believed to contribute significantly to these bioactivities by facilitating specific interactions with biological targets. This has prompted further investigation into its potential as a lead compound for drug discovery programs.

The synthesis of Benzaldehyde,4,4'-(2,5-thiophenediyl)bis-(9CI) involves multi-step organic reactions that highlight the compound's complexity and synthetic utility. Advanced synthetic methodologies have been employed to achieve high yields and purity levels, ensuring that the compound meets the stringent requirements for industrial and research applications. Techniques such as palladium-catalyzed cross-coupling reactions have been particularly useful in constructing the intricate molecular framework of this compound.

The impact of Benzaldehyde,4,4'-(2,5-thiophenediyl)bis-(9CI) extends beyond its direct applications. It serves as a crucial reference point for researchers studying related compounds and their derivatives. The structural features and reactivity patterns observed in this compound provide valuable insights into the design and optimization of new molecules with enhanced functionalities. This underscores its importance not only as a chemical entity but also as a catalyst for innovation in synthetic chemistry.

In conclusion, Benzaldehyde,4,4'-(2,5-thiophenediyl)bis-(9CI), identified by its CAS number 193903-62-7, represents a significant advancement in modern chemical research. Its unique structural features and versatile reactivity make it indispensable in various fields ranging from pharmaceuticals to material science. The ongoing exploration of its applications continues to reveal new possibilities for its use as an intermediate and lead compound for innovative research projects.

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