3-Bromo-5-(tert-butyl)benzo[b]thiophene
97%
- Product Code: 65125
CAS:
1780644-81-6
| Molecular Weight: | 269.20 g./mol | Molecular Formula: | C₁₂H₁₃BrS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28593666 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, away from light, dry, sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring a bromine atom and a tert-butyl group on a benzo[b]thiophene core, makes it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse compounds with potential biological activity. Additionally, the tert-butyl group can enhance the stability and lipophilicity of the resulting molecules, which is advantageous in drug design. This compound is also explored in materials science for the development of organic semiconductors and optoelectronic materials due to its conjugated thiophene ring system.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to light yellow Liquid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $19.93 |
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| 1.000 | 10-20 days | $58.97 |
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| 5.000 | 10-20 days | $212.63 |
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| 25.000 | 10-20 days | $752.51 |
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3-Bromo-5-(tert-butyl)benzo[b]thiophene
This chemical is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring a bromine atom and a tert-butyl group on a benzo[b]thiophene core, makes it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. The bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse compounds with potential biological activity. Additionally, the tert-butyl group can enhance the stability and lipophilicity of the resulting molecules, which is advantageous in drug design. This compound is also explored in materials science for the development of organic semiconductors and optoelectronic materials due to its conjugated thiophene ring system.
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