Methyl 5-((tert-butoxycarbonyl)amino)-4-nitrothiophene-2-carboxylate
97%
- Product Code: 48108
CAS:
1351238-59-9
| Molecular Weight: | 302.30 g./mol | Molecular Formula: | C₁₁H₁₄N₂O₆S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30833848 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both a nitro group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of pharmaceuticals and agrochemicals. The nitro group allows for further functionalization through reduction or substitution reactions, while the Boc group can be deprotected to reveal a free amine, enabling coupling reactions. It is particularly useful in the synthesis of thiophene-based compounds, which are often explored for their biological activities, such as antimicrobial, anti-inflammatory, or anticancer properties. Additionally, its ester group provides a handle for further chemical modifications, making it versatile in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,232.00 |
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| 0.250 | 10-20 days | ฿22,464.00 |
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Methyl 5-((tert-butoxycarbonyl)amino)-4-nitrothiophene-2-carboxylate
This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both a nitro group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of pharmaceuticals and agrochemicals. The nitro group allows for further functionalization through reduction or substitution reactions, while the Boc group can be deprotected to reveal a free amine, enabling coupling reactions. It is particularly useful in the synthesis of thiophene-based compounds, which are often explored for their biological activities, such as antimicrobial, anti-inflammatory, or anticancer properties. Additionally, its ester group provides a handle for further chemical modifications, making it versatile in medicinal chemistry and drug discovery.
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