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Catalog Number:
42694
CAS Number:
3541-37-5
Benzo[b]thiophene-2-carboxaldehyde
Purity:
≥ 98% (GC)
Synonym(s):
2-Formylbenzo[b]thiophene
Documents
$81.42 /5G
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Product Information

Benzo[b]thiophene-2-carboxaldehyde is a versatile compound recognized for its unique structure and functional properties, making it a valuable asset in various fields such as organic synthesis and materials science. This compound, also known as 1-benzothiophene-2-carbaldehyde, features a benzothiophene backbone that enhances its reactivity and stability, allowing it to serve as an essential building block in the synthesis of complex organic molecules. Its aldehyde functional group provides opportunities for further chemical modifications, facilitating the development of novel pharmaceuticals and agrochemicals.

In the realm of research and industry, Benzo[b]thiophene-2-carboxaldehyde is particularly useful in the synthesis of heterocyclic compounds and as an intermediate in the production of dyes and pigments. Its unique properties enable it to be employed in the development of advanced materials, including organic semiconductors and sensors. Researchers appreciate its potential for creating innovative solutions, making it a sought-after compound in laboratories and production facilities alike.

Synonyms
2-Formylbenzo[b]thiophene
CAS Number
3541-37-5
Purity
≥ 98% (GC)
Molecular Formula
C9H6OS
Molecular Weight
162.21
MDL Number
MFCD01075041
PubChem ID
736500
Melting Point
35 °C
Appearance
White to orange to green powder or lump
Boiling Point
136 °C/8 mmHg
Conditions
Store at RT
General Information
Synonyms
2-Formylbenzo[b]thiophene
CAS Number
3541-37-5
Purity
≥ 98% (GC)
Molecular Formula
C9H6OS
Molecular Weight
162.21
MDL Number
MFCD01075041
PubChem ID
736500
Melting Point
35 °C
Appearance
White to orange to green powder or lump
Boiling Point
136 °C/8 mmHg
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Benzo[b]thiophene-2-carboxaldehyde is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, including pharmaceuticals and agrochemicals, due to its unique structure that allows for diverse chemical reactions.
  • Material Science: It is used in the development of advanced materials, particularly in the creation of conductive polymers and organic semiconductors, which are essential for electronic devices.
  • Pharmaceutical Development: Researchers explore its potential in drug discovery, particularly for compounds targeting specific biological pathways, enhancing the efficacy of treatments.
  • Fluorescent Probes: The compound is employed in the design of fluorescent probes for biological imaging, providing researchers with tools to visualize cellular processes in real-time.
  • Environmental Chemistry: It plays a role in studying environmental pollutants, helping to develop methods for detecting and analyzing thiophene derivatives in various ecosystems.

Citations