tert-Butyl (2-amino-3-methylphenyl)carbamate
95%
- Product Code: 36363
CAS:
954238-92-7
| Molecular Weight: | 222.2835 g./mol | Molecular Formula: | C₁₂H₁₈N₂O₂ |
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| EC Number: | MDL Number: | MFCD09701247 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
tert-Butyl (2-amino-3-methylphenyl)carbamate is primarily used in organic synthesis as an intermediate for the preparation of more complex chemical compounds. It is particularly valuable in the pharmaceutical industry, where it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs). The compound's structure, featuring both an amino group and a carbamate moiety, makes it versatile for constructing molecules with potential biological activity. Additionally, it is utilized in research and development for creating novel compounds with applications in medicinal chemistry, such as inhibitors or modulators of specific biological targets. Its stability and reactivity under various conditions make it a useful reagent in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,597.00 |
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tert-Butyl (2-amino-3-methylphenyl)carbamate
tert-Butyl (2-amino-3-methylphenyl)carbamate is primarily used in organic synthesis as an intermediate for the preparation of more complex chemical compounds. It is particularly valuable in the pharmaceutical industry, where it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs). The compound's structure, featuring both an amino group and a carbamate moiety, makes it versatile for constructing molecules with potential biological activity. Additionally, it is utilized in research and development for creating novel compounds with applications in medicinal chemistry, such as inhibitors or modulators of specific biological targets. Its stability and reactivity under various conditions make it a useful reagent in multi-step synthetic processes.
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