Methyl 2-((tert-butoxycarbonyl)amino)-2-(4-chlorophenyl)acetate
95%
- Product Code: 67222
CAS:
1273585-66-2
| Molecular Weight: | 299.75 g./mol | Molecular Formula: | C₁₄H₁₈ClNO₄ |
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| EC Number: | MDL Number: | MFCD24444872 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that target specific diseases. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it a valuable intermediate in organic synthesis. It is often employed in peptide coupling reactions, where the Boc group protects the amino functionality during the synthesis process, ensuring selective reactions. Additionally, the presence of the chlorophenyl group enhances its utility in creating compounds with potential biological activity, such as inhibitors or receptor modulators. Its application extends to medicinal chemistry research, where it aids in the design and optimization of drug candidates with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $131.66 |
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| 0.250 | 10-20 days | $239.26 |
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| 1.000 | 10-20 days | $562.40 |
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Methyl 2-((tert-butoxycarbonyl)amino)-2-(4-chlorophenyl)acetate
This chemical is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that target specific diseases. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a chlorophenyl moiety, makes it a valuable intermediate in organic synthesis. It is often employed in peptide coupling reactions, where the Boc group protects the amino functionality during the synthesis process, ensuring selective reactions. Additionally, the presence of the chlorophenyl group enhances its utility in creating compounds with potential biological activity, such as inhibitors or receptor modulators. Its application extends to medicinal chemistry research, where it aids in the design and optimization of drug candidates with improved efficacy and selectivity.
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