tert-Butyl (5-amino-2-methylphenyl)carbamate
97%
- Product Code: 148718
CAS:
329763-32-8
| Molecular Weight: | 222.28 g./mol | Molecular Formula: | C₁₂H₁₈N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04114553 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in inert gas |
Product Description:
Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where protected amine functionalities are required. The tert-butoxycarbonyl (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions, making it ideal for multi-step synthesis. It is commonly employed in the preparation of kinase inhibitors, anti-inflammatory agents, and other bioactive molecules. Its aromatic amine structure allows for further functionalization via coupling reactions, enabling the construction of complex drug-like structures. Also utilized in research settings for the synthesis of labeled compounds in metabolic studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿950.00 |
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| 1g | 10-20 days | ฿2,010.00 |
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| 5g | 10-20 days | ฿8,890.00 |
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| 25g | 10-20 days | ฿43,750.00 |
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tert-Butyl (5-amino-2-methylphenyl)carbamate
Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where protected amine functionalities are required. The tert-butoxycarbonyl (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions, making it ideal for multi-step synthesis. It is commonly employed in the preparation of kinase inhibitors, anti-inflammatory agents, and other bioactive molecules. Its aromatic amine structure allows for further functionalization via coupling reactions, enabling the construction of complex drug-like structures. Also utilized in research settings for the synthesis of labeled compounds in metabolic studies.
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