6-Bromobenzo[b]thiophene-2-carbonitrile
≥95%
- Product Code: 81542
CAS:
1190198-24-3
Molecular Weight: | 238.10 g./mol | Molecular Formula: | C₉H₄BrNS |
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EC Number: | MDL Number: | MFCD12922709 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
6-Bromobenzo[b]thiophene-2-carbonitrile is primarily used in organic synthesis as a versatile intermediate for the development of various heterocyclic compounds. Its structure, featuring both a bromine atom and a nitrile group, makes it a valuable building block in the construction of complex molecules, particularly in pharmaceutical research. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce the benzo[b]thiophene moiety into larger molecular frameworks. This compound is also utilized in the synthesis of potential drug candidates, especially those targeting neurological disorders or cancer, due to its ability to interact with biological targets. Additionally, it serves as a precursor in the preparation of organic materials, such as conjugated polymers or small molecules for optoelectronic applications, where the benzo[b]thiophene unit can enhance electronic properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,895.00 |
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0.250 | 10-20 days | ฿10,323.00 |
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1.000 | 10-20 days | ฿23,031.00 |
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6-Bromobenzo[b]thiophene-2-carbonitrile
6-Bromobenzo[b]thiophene-2-carbonitrile is primarily used in organic synthesis as a versatile intermediate for the development of various heterocyclic compounds. Its structure, featuring both a bromine atom and a nitrile group, makes it a valuable building block in the construction of complex molecules, particularly in pharmaceutical research. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce the benzo[b]thiophene moiety into larger molecular frameworks. This compound is also utilized in the synthesis of potential drug candidates, especially those targeting neurological disorders or cancer, due to its ability to interact with biological targets. Additionally, it serves as a precursor in the preparation of organic materials, such as conjugated polymers or small molecules for optoelectronic applications, where the benzo[b]thiophene unit can enhance electronic properties.
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