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Catalog Number:
44170
CAS Number:
39827-11-7
Benzo[b]thiophene-2-carbonyl chloride
Purity:
≥ 95% (NMR)
Hazmat
Documents
$73.21 /1G
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Product Information

Benzo[b]thiophene-2-carbonyl chloride is a versatile chemical compound widely utilized in organic synthesis and pharmaceutical development. This compound, characterized by its unique structure, serves as an essential intermediate in the synthesis of various bioactive molecules, particularly in the creation of thiophene-based pharmaceuticals. Its reactivity as an acyl chloride allows for efficient acylation reactions, making it a valuable building block in the development of complex organic compounds. Researchers and industry professionals appreciate its role in the synthesis of agrochemicals and fine chemicals, where it can be employed to enhance the efficacy of active ingredients.

The compound's distinctive properties, including its ability to undergo nucleophilic substitution reactions, further expand its applicability in synthetic chemistry. Its use in the preparation of thiophene derivatives has shown promising results in medicinal chemistry, particularly in the development of new therapeutic agents. With its potential to streamline synthetic pathways and improve yields, Benzo[b]thiophene-2-carbonyl chloride stands out as a crucial reagent for researchers aiming to innovate in drug discovery and development.

CAS Number
39827-11-7
Purity
≥ 95% (NMR)
Molecular Formula
C9H5ClOS
Molecular Weight
196.65
MDL Number
MFCD00051635
PubChem ID
142384
Melting Point
83 - 88 °C (Lit.)
Appearance
White solid
Boiling Point
176 °C/17 mmHg (Lit.)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
39827-11-7
Purity
≥ 95% (NMR)
Molecular Formula
C9H5ClOS
Molecular Weight
196.65
MDL Number
MFCD00051635
PubChem ID
142384
Melting Point
83 - 88 °C (Lit.)
Appearance
White solid
Boiling Point
176 °C/17 mmHg (Lit.)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Synthetic Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, enabling researchers to create complex molecules efficiently.
  • Material Science: It is used in the development of advanced materials, such as polymers and coatings, that require specific chemical properties for improved durability and performance.
  • Organic Electronics: The compound plays a significant role in the fabrication of organic semiconductors, which are essential for the production of flexible electronic devices and solar cells.
  • Biological Research: Researchers utilize it to explore its potential as a bioactive compound, investigating its effects on biological systems and its possible applications in drug development.
  • Environmental Chemistry: It is also studied for its role in the degradation of pollutants, providing insights into how to mitigate environmental impact through chemical processes.

Citations