tert-Butyl 2-(4-bromophenyl)propan-2-ylcarbamate
≥95%
- Product Code: 126293
CAS:
214973-83-8
| Molecular Weight: | 314.22 g./mol | Molecular Formula: | C14H20BrNO2 |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16619489 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate in the production of pharmaceuticals and agrochemicals. It serves as a building block for the development of compounds with potential biological activity, particularly in the synthesis of active pharmaceutical ingredients (APIs). Its structure, featuring a bromophenyl group and a carbamate moiety, makes it valuable for constructing more complex molecules through reactions such as cross-coupling or functional group transformations. Additionally, it is employed in research settings for the development of new drug candidates, especially in the fields of central nervous system (CNS) disorders and anti-inflammatory agents. Its stability and reactivity make it a versatile reagent in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €12.19 |
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| 0.250 | 10-20 days | €41.42 |
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| 1.000 | 10-20 days | €164.10 |
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| 5.000 | 10-20 days | €661.13 |
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tert-Butyl 2-(4-bromophenyl)propan-2-ylcarbamate
This chemical is primarily utilized in organic synthesis as a key intermediate in the production of pharmaceuticals and agrochemicals. It serves as a building block for the development of compounds with potential biological activity, particularly in the synthesis of active pharmaceutical ingredients (APIs). Its structure, featuring a bromophenyl group and a carbamate moiety, makes it valuable for constructing more complex molecules through reactions such as cross-coupling or functional group transformations. Additionally, it is employed in research settings for the development of new drug candidates, especially in the fields of central nervous system (CNS) disorders and anti-inflammatory agents. Its stability and reactivity make it a versatile reagent in medicinal chemistry.
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