Cas no 1128-88-7 (1-(Benzobthiophen-5-yl)ethan-1-one)

1-(Benzothiophen-5-yl)ethan-1-one is a heterocyclic aromatic ketone featuring a benzothiophene core substituted with an acetyl group at the 5-position. This compound serves as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and functional materials. Its benzothiophene scaffold imparts stability and electronic properties conducive to further functionalization, while the acetyl group offers a reactive site for derivatization via condensation, reduction, or nucleophilic addition. The product exhibits high purity and consistent performance, making it suitable for research and industrial applications requiring precise molecular building blocks. Its structural attributes contribute to its utility in constructing complex heterocyclic systems with potential biological activity.
1-(Benzobthiophen-5-yl)ethan-1-one structure
1128-88-7 structure
Product Name:1-(Benzobthiophen-5-yl)ethan-1-one
CAS No:1128-88-7
MF:C10H8OS
MW:176.234921455383
MDL:MFCD16619666
CID:1200768
PubChem ID:14358678
Update Time:2025-10-29

1-(Benzobthiophen-5-yl)ethan-1-one Chemical and Physical Properties

Names and Identifiers

    • Ethanone, 1-benzo[b]thien-5-yl-
    • 1-(1-benzothiophen-5-yl)ethanone
    • 1-(1-Benzothiophen-5-yl)ethan-1-one
    • 1-(benzo[b]thiophen-5-yl)ethanone
    • A802586
    • DB-421423
    • AKOS015897660
    • 5-Acetylbenzothiophene
    • CS-0088175
    • AS-40026
    • 1128-88-7
    • DTXSID80559324
    • EN300-2057499
    • 1-(benzo[b]thiophen-5-yl)ethan-1-one
    • SCHEMBL826934
    • BAA12888
    • 1-(benzo[b]thiophen-5-yl]ethan-1-one
    • LYPSYIWSZQVHAB-UHFFFAOYSA-N
    • 1-Benzo[b]thien-5-ylethanone
    • MFCD16619666
    • 1-(Benzobthiophen-5-yl)ethan-1-one
    • MDL： MFCD16619666
    • Inchi： 1S/C10H8OS/c1-7(11)8-2-3-10-9(6-8)4-5-12-10/h2-6H,1H3
    • InChI Key： LYPSYIWSZQVHAB-UHFFFAOYSA-N
    • SMILES： S1C=CC2C=C(C(C)=O)C=CC1=2

Computed Properties

  • Exact Mass: 176.02964
  • Monoisotopic Mass: 176.02958605g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 190
  • 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: 2.8
  • Topological Polar Surface Area: 45.3?2

Experimental Properties

  • PSA: 17.07

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1-(Benzobthiophen-5-yl)ethan-1-one Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:1128-88-7)1-(Benzobthiophen-5-yl)ethan-1-one
Order Number:A1154043
Stock Status:in Stock
Quantity:5g
Purity:99%
Pricing Information Last Updated:Thursday, 29 August 2024 23:23
Price ($):1202.0

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Additional information on 1-(Benzobthiophen-5-yl)ethan-1-one

1-(Benzobthiophen-5-yl)ethan-1-one: A Comprehensive Overview

1-(Benzobthiophen-5-yl)ethan-1-one, also known by its CAS number 1128-88-7, is a compound of significant interest in the fields of organic chemistry, materials science, and pharmacology. This compound is a derivative of benzobthiophene, a heterocyclic aromatic compound, with a ketone functional group attached at the 5-position. The structure of this compound is characterized by a fused bicyclic system consisting of a benzene ring and a thiophene ring, with the ketone group providing additional reactivity and functional versatility.

The synthesis of 1-(Benzobthiophen-5-yl)ethan-1-one typically involves multi-step organic reactions, often utilizing coupling reactions or oxidation processes. Recent advancements in catalytic methods have enabled more efficient and selective syntheses, which are crucial for scaling up production in both academic and industrial settings. The compound's stability under various conditions makes it suitable for applications in high-performance materials and advanced drug delivery systems.

From a physical standpoint, 1-(Benzobthiophen-5-yl)ethan-1-one exhibits unique electronic properties due to its conjugated π-system. These properties have been leveraged in the development of novel optoelectronic materials, such as organic light-emitting diodes (OLEDs) and photovoltaic devices. Recent studies have demonstrated that the compound's ability to absorb and emit light at specific wavelengths can be tuned through structural modifications, opening new avenues for customized optical applications.

In the realm of pharmacology, 1-(Benzobthiophen-5-yl)ethan-1-one has shown potential as a lead compound for drug development. Its ability to interact with specific biological targets has been explored in various disease models, including cancer and neurodegenerative disorders. Researchers have reported that the compound's bioavailability and pharmacokinetic profile can be optimized through chemical modifications, enhancing its therapeutic potential.

The environmental impact of 1-(Benzobthiophen-5-yl)ethan-1-one has also been a topic of recent investigation. Studies suggest that the compound degrades under certain environmental conditions, but its persistence in specific ecosystems requires further scrutiny. As industries increasingly prioritize sustainability, understanding the environmental fate of this compound is essential for responsible chemical management.

In conclusion, 1-(Benzobthiophen-5-yl)ethan-1-one, with its unique chemical structure and versatile properties, continues to be a focal point in diverse scientific disciplines. Ongoing research into its synthesis, applications, and environmental behavior underscores its importance as a multifaceted chemical entity. As new discoveries emerge, this compound is poised to play an even greater role in advancing technological and therapeutic innovations.

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Amadis Chemical Company Limited
(CAS:1128-88-7)1-(Benzobthiophen-5-yl)ethan-1-one
A1154043
Purity:99%
Quantity:5g
Price ($):1202.0
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