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Catalog Number:
44272
CAS Number:
135-00-2
2-Benzoylthiophene
Purity:
≥ 98% (GC)
Synonym(s):
Phenyl 2-thienyl ketone
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Product Information

2-Benzoylthiophene is a versatile compound known for its unique properties and applications in various fields, particularly in organic synthesis and material science. This aromatic ketone features a thiophene ring, which enhances its reactivity and makes it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and dyes. Its ability to undergo various chemical transformations allows researchers to utilize it in the development of novel compounds with specific functionalities.

In the pharmaceutical industry, 2-Benzoylthiophene has been explored for its potential as a building block in the synthesis of biologically active molecules, contributing to the discovery of new therapeutic agents. Additionally, its photochemical properties make it suitable for applications in organic electronics, such as organic light-emitting diodes (OLEDs) and solar cells. With its distinctive structure and reactivity, 2-Benzoylthiophene stands out as a crucial compound for researchers and industry professionals seeking innovative solutions in their respective fields.

Synonyms
Phenyl 2-thienyl ketone
CAS Number
135-00-2
Purity
≥ 98% (GC)
Molecular Formula
C11H8OS
Molecular Weight
188.24
MDL Number
MFCD00022495
PubChem ID
67262
Melting Point
55 - 57 °C
Appearance
Light yellow to amber to dark green crystalline powder
Boiling Point
300 °C
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Phenyl 2-thienyl ketone
CAS Number
135-00-2
Purity
≥ 98% (GC)
Molecular Formula
C11H8OS
Molecular Weight
188.24
MDL Number
MFCD00022495
PubChem ID
67262
Melting Point
55 - 57 °C
Appearance
Light yellow to amber to dark green crystalline powder
Boiling Point
300 °C
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Benzoylthiophene is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, allowing researchers to create complex molecules for pharmaceuticals and agrochemicals.
  • Photochemical Applications: It is used in photochemistry to study light-induced reactions, making it valuable for developing new materials in the solar energy sector.
  • Fluorescent Dyes: 2-Benzoylthiophene can be incorporated into fluorescent dyes, enhancing imaging techniques in biological research and diagnostics.
  • Material Science: The compound is explored for its properties in developing advanced materials, such as polymers with enhanced thermal stability and electrical conductivity.
  • Pharmaceutical Development: It has potential applications in drug design, particularly in creating compounds that target specific biological pathways, offering advantages over traditional methods.

Citations