tert-Butyl (4,5-dibromothiophen-2-yl)carbamate
97%
- Product Code: 36806
CAS:
943321-93-5
| Molecular Weight: | 357.06 g./mol | Molecular Formula: | C₉H₁₁Br₂NO₂S |
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| EC Number: | MDL Number: | MFCD25969363 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block for more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a dibromothiophene core, makes it a valuable intermediate for constructing heterocyclic compounds, which are often key components in active pharmaceutical ingredients. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing for selective reactions in multi-step synthetic processes. It is also employed in the synthesis of materials with potential applications in organic electronics due to the thiophene moiety’s conductive properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,750.00 |
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| 0.250 | 10-20 days | ฿13,500.00 |
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tert-Butyl (4,5-dibromothiophen-2-yl)carbamate
This chemical is primarily utilized in organic synthesis as a building block for more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a dibromothiophene core, makes it a valuable intermediate for constructing heterocyclic compounds, which are often key components in active pharmaceutical ingredients. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing for selective reactions in multi-step synthetic processes. It is also employed in the synthesis of materials with potential applications in organic electronics due to the thiophene moiety’s conductive properties.
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