tert-Butyl 5-bromo-2-methyl-1H-benzo[d]imidazole-1-carboxylate
97%
- Product Code: 192454
CAS:
1038392-63-0
| Molecular Weight: | 311.17 g./mol | Molecular Formula: | C₁₃H₁₅BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD30067358 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization at the bromo position, enabling coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aromatic or heteroaromatic groups. The tert-butoxycarbonyl (Boc) protecting group stabilizes the imidazole nitrogen during multi-step syntheses and can be easily removed under mild acidic conditions when needed. Commonly employed in medicinal chemistry for constructing bioactive molecules targeting inflammation, cancer, and central nervous system disorders.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿6,990.00 |
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| 1.000 G | 10-20 days | ฿19,020.00 |
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| 0.100 G | 10-20 days | ฿3,960.00 |
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tert-Butyl 5-bromo-2-methyl-1H-benzo[d]imidazole-1-carboxylate
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for selective functionalization at the bromo position, enabling coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aromatic or heteroaromatic groups. The tert-butoxycarbonyl (Boc) protecting group stabilizes the imidazole nitrogen during multi-step syntheses and can be easily removed under mild acidic conditions when needed. Commonly employed in medicinal chemistry for constructing bioactive molecules targeting inflammation, cancer, and central nervous system disorders.
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