tert-Butyl 3-(hydroxymethyl)-7-nitro-1H-indole-1-carboxylate
≥95%
- Product Code: 114547
CAS:
914349-15-8
Molecular Weight: | 292.29 g./mol | Molecular Formula: | C₁₄H₁₆N₂O₅ |
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EC Number: | MDL Number: | MFCD05864725 | |
Melting Point: | Boiling Point: | 470.2°C at 760 mmHg | |
Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry research. It serves as a key intermediate in the development of indole-based pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. Its structure, featuring a nitro group and a hydroxylmethyl group, makes it a versatile building block for modifying indole derivatives, which are often explored for their therapeutic properties. Researchers use it to create novel molecules for drug discovery, especially in areas like anti-inflammatory, anticancer, and antimicrobial agents. Additionally, it can be employed in the study of enzyme inhibitors or receptor modulators due to its reactive functional groups.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,773.00 |
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1.000 | 10-20 days | ฿4,392.00 |
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5.000 | 10-20 days | ฿16,632.00 |
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10.000 | 10-20 days | ฿24,966.00 |
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tert-Butyl 3-(hydroxymethyl)-7-nitro-1H-indole-1-carboxylate
This compound is primarily utilized in organic synthesis and medicinal chemistry research. It serves as a key intermediate in the development of indole-based pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. Its structure, featuring a nitro group and a hydroxylmethyl group, makes it a versatile building block for modifying indole derivatives, which are often explored for their therapeutic properties. Researchers use it to create novel molecules for drug discovery, especially in areas like anti-inflammatory, anticancer, and antimicrobial agents. Additionally, it can be employed in the study of enzyme inhibitors or receptor modulators due to its reactive functional groups.
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