Tert-Butyl (2-(4-bromo-1h-pyrazol-1-yl)ethyl)carbamate
95%
- Product Code: 41663
CAS:
1435753-36-8
| Molecular Weight: | 290.16 g./mol | Molecular Formula: | C₁₀H₁₆BrN₃O₂ |
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| EC Number: | MDL Number: | MFCD30284939 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex compounds. Its structure, featuring a pyrazole ring and a carbamate group, makes it valuable in medicinal chemistry for designing and synthesizing potential pharmaceutical agents. It is often employed in the preparation of biologically active molecules, particularly in the research and development of drugs targeting various diseases. Additionally, the presence of a bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Its stability and reactivity make it a useful building block in the synthesis of heterocyclic compounds, which are crucial in many therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,348.00 |
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| 0.250 | 10-20 days | ฿20,592.00 |
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| 1.000 | 10-20 days | ฿54,792.00 |
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Tert-Butyl (2-(4-bromo-1h-pyrazol-1-yl)ethyl)carbamate
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex compounds. Its structure, featuring a pyrazole ring and a carbamate group, makes it valuable in medicinal chemistry for designing and synthesizing potential pharmaceutical agents. It is often employed in the preparation of biologically active molecules, particularly in the research and development of drugs targeting various diseases. Additionally, the presence of a bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Its stability and reactivity make it a useful building block in the synthesis of heterocyclic compounds, which are crucial in many therapeutic applications.
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