4-Bromo-N,N-Dimethylbenzamide
98%
- Product Code: 77270
CAS:
18469-37-9
| Molecular Weight: | 228.10 g./mol | Molecular Formula: | C₉H₁₀BrNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00463696 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its bromo and amide functional groups make it a versatile building block for constructing more complex molecules. It is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific structural motifs into drug candidates. Additionally, it serves as a precursor in the synthesis of dyes, pigments, and other specialty chemicals. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is particularly significant in creating carbon-carbon or carbon-nitrogen bonds, which are essential in medicinal chemistry and material science.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white to light yellow solid |
| PURITY | 97.5-100 |
| PROTON NMR SPECTRUM | Conforms to Structure |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft13,790.86 |
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| 1.000 | 10-20 days | Ft49,884.12 |
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| 5.000 | 10-20 days | Ft81,129.03 |
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| 25.000 | 10-20 days | Ft350,373.99 |
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4-Bromo-N,N-Dimethylbenzamide
This chemical is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its bromo and amide functional groups make it a versatile building block for constructing more complex molecules. It is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific structural motifs into drug candidates. Additionally, it serves as a precursor in the synthesis of dyes, pigments, and other specialty chemicals. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is particularly significant in creating carbon-carbon or carbon-nitrogen bonds, which are essential in medicinal chemistry and material science.
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