Cas no 1220-08-2 (Benzaldehyde, 4,4'-(1,2-ethanediyl)bis-)

Benzaldehyde, 4,4'-(1,2-ethanediyl)bis-, is a bifunctional aromatic aldehyde characterized by its ethylene-linked benzaldehyde groups. This compound is primarily utilized in organic synthesis, serving as a key intermediate for the preparation of pharmaceuticals, agrochemicals, and specialty polymers. Its rigid molecular structure and dual aldehyde functionality enable efficient cross-linking and condensation reactions, making it valuable in the synthesis of heterocyclic compounds and Schiff bases. The compound exhibits high purity and stability under standard conditions, ensuring consistent performance in demanding applications. Its well-defined reactivity profile allows for precise control in multi-step synthetic processes, contributing to its utility in advanced chemical research and industrial applications.
Benzaldehyde, 4,4'-(1,2-ethanediyl)bis- structure
1220-08-2 structure
Product Name:Benzaldehyde, 4,4'-(1,2-ethanediyl)bis-
CAS No:1220-08-2
MF:C16H14O2
MW:238.281164646149
CID:1213684
PubChem ID:4134131
Update Time:2025-10-24

Benzaldehyde, 4,4'-(1,2-ethanediyl)bis- Chemical and Physical Properties

Names and Identifiers

    • Benzaldehyde, 4,4'-(1,2-ethanediyl)bis-
    • 4-[2-(4-formylphenyl)ethyl]benzaldehyde
    • 4,4'-(Ethane-1,2-diyl)dibenzaldehyde
    • 1,2-bis-(4-formylphenyl)ethane
    • AKOS028111845
    • 4,4'-ethane-1,2-diyldibenzaldehyde
    • starbld0019361
    • SCHEMBL5429778
    • 1220-08-2
    • DTXSID60399720
    • AT24218
    • Inchi: 1S/C16H14O2/c17-11-15-7-3-13(4-8-15)1-2-14-5-9-16(12-18)10-6-14/h3-12H,1-2H2
    • InChI Key: OIFGRECGCKJKMR-UHFFFAOYSA-N
    • SMILES: O=CC1C=CC(=CC=1)CCC1C=CC(C=O)=CC=1

Computed Properties

  • Exact Mass: 270.08922
  • Monoisotopic Mass: 238.099
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 5
  • Complexity: 230
  • 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: 3.1
  • Topological Polar Surface Area: 34.1?2

Experimental Properties

  • PSA: 74.6

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Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI XIAN DING Biotechnology Co., Ltd.
X194352A-1g
Benzaldehyde, 4,4'-(1,2-ethanediyl)bis-
1220-08-2 0.98
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SHANG HAI XIAN DING Biotechnology Co., Ltd.
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Additional information on Benzaldehyde, 4,4'-(1,2-ethanediyl)bis-

Benzaldehyde, 4,4'-(1,2-ethanediyl)bis- and Its Significance in Modern Chemical Research

Benzaldehyde, 4,4'-(1,2-ethanediyl)bis-, a compound with the CAS number 1220-08-2, represents a fascinating molecule in the realm of organic chemistry. This bifunctional benzaldehyde derivative has garnered significant attention due to its unique structural properties and versatile applications in various scientific domains. The presence of two benzaldehyde units linked by a 1,2-ethanediyl bridge imparts distinct reactivity and functionality, making it a valuable intermediate in synthetic chemistry.

The chemical structure of Benzaldehyde, 4,4'-(1,2-ethanediyl)bis- can be described as a linear dimer where each benzaldehyde moiety contributes an aldehyde group (–CHO) at the para position relative to the central ethylene bridge. This configuration allows for multiple reaction pathways, including condensation reactions with various nucleophiles, polymerization processes, and cross-coupling reactions. Such versatility has positioned this compound as a key player in the development of novel materials and pharmaceuticals.

In recent years, researchers have been exploring the potential of Benzaldehyde, 4,4'-(1,2-ethanediyl)bis- in the synthesis of advanced polymers. The bifunctional nature of this molecule enables the formation of polymers with controlled architectures and enhanced properties. For instance, it has been utilized in the preparation of polyimides and polyamides through step-growth polymerization. These polymers exhibit excellent thermal stability and mechanical strength, making them suitable for high-performance applications in electronics and aerospace industries.

Moreover, the aldehyde groups in Benzaldehyde, 4,4'-(1,2-ethanediyl)bis- provide opportunities for further functionalization. Researchers have leveraged these groups to introduce additional functionalities such as hydroxyl or amino groups via condensation reactions. This approach has led to the development of novel biomaterials with applications in drug delivery systems and tissue engineering. The ability to tailor the molecular structure of these materials by incorporating different functional groups has opened up new avenues for therapeutic interventions.

The pharmaceutical industry has also shown interest in Benzaldehyde, 4,4'-(1,2-ethanediyl)bis- due to its potential as a precursor for bioactive molecules. The compound’s ability to undergo various chemical transformations allows for the synthesis of complex scaffolds that mimic natural products. Recent studies have demonstrated its utility in generating derivatives with antimicrobial and anti-inflammatory properties. These findings highlight the compound’s role as a building block in medicinal chemistry.

Another area where Benzaldehyde, 4,4'-(1,2-ethanediyl)bis- has made significant contributions is in the field of organic electronics. The development of conductive polymers and organic semiconductors relies heavily on carefully designed molecular architectures. The use of this compound as a monomer or intermediate has enabled the synthesis of materials with improved charge transport properties. Such advancements are crucial for the development of flexible electronics and organic photovoltaic devices.

The environmental impact of chemical processes is another consideration that has driven research into sustainable applications of Benzaldehyde, 4,4'-(1,2-ethanediyl)bis. Efforts have been made to develop green synthetic routes that minimize waste and reduce energy consumption. For example, catalytic methods have been explored to facilitate the formation of the ethylene bridge without harsh reagents or high temperatures. These innovations align with global efforts to promote sustainable chemistry practices.

In conclusion, Benzaldehyde, 4,4'-(1,2-ethanediyl)bis stands out as a versatile compound with broad applications across multiple scientific disciplines. Its unique structure and reactivity make it an invaluable tool for synthetic chemists working on polymers、pharmaceuticals、and organic electronics. As research continues to uncover new possibilities,this molecule is poised to play an even greater role in advancing chemical science and technology.

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