tert-Butyl 6-aminoindoline-1-carboxylate
98%
- Product Code: 149710
CAS:
129488-00-2
| Molecular Weight: | 234.29 g./mol | Molecular Formula: | C₁₃H₁₈N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08059271 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed, light-proof |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery. Commonly employed in the preparation of indoline-based scaffolds found in anticancer, antiviral, and anti-inflammatory agents. The tert-butyloxycarbonyl (Boc) protection enables compatibility with a wide range of reaction conditions, facilitating peptide coupling and heterocycle formation. Widely applied in medicinal chemistry for building complex nitrogen-containing molecules.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Gray to brown solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,280.00 |
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| 250mg | 10-20 days | ฿2,260.00 |
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| 1g | 10-20 days | ฿5,800.00 |
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| 5g | 10-20 days | ฿19,800.00 |
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tert-Butyl 6-aminoindoline-1-carboxylate
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug discovery. Commonly employed in the preparation of indoline-based scaffolds found in anticancer, antiviral, and anti-inflammatory agents. The tert-butyloxycarbonyl (Boc) protection enables compatibility with a wide range of reaction conditions, facilitating peptide coupling and heterocycle formation. Widely applied in medicinal chemistry for building complex nitrogen-containing molecules.
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| Stable in pH range | - |
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