2-((tert-Butoxycarbonyl)amino)-2-(4-chlorophenyl)acetic acid
97%
- Product Code: 54909
CAS:
209525-73-5
| Molecular Weight: | 285.72 g./mol | Molecular Formula: | C₁₃H₁₆ClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03426366 | |
| Melting Point: | Boiling Point: | 438.8°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the production of peptide-based drugs, where the tert-butoxycarbonyl (Boc) group acts as a protective group for amines during peptide coupling reactions. Its structure, featuring a 4-chlorophenyl group, makes it valuable in the development of compounds with potential therapeutic properties, particularly in targeting specific biological pathways or receptors. Additionally, it is employed in organic synthesis for constructing complex molecules, especially in medicinal chemistry research aimed at discovering new drugs or optimizing existing ones.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | £29.92 |
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| 1.000 | 10-20 days | £65.14 |
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| 5.000 | 10-20 days | £224.32 |
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| 10.000 | 10-20 days | £408.53 |
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2-((tert-Butoxycarbonyl)amino)-2-(4-chlorophenyl)acetic acid
This chemical is primarily utilized in the synthesis of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the production of peptide-based drugs, where the tert-butoxycarbonyl (Boc) group acts as a protective group for amines during peptide coupling reactions. Its structure, featuring a 4-chlorophenyl group, makes it valuable in the development of compounds with potential therapeutic properties, particularly in targeting specific biological pathways or receptors. Additionally, it is employed in organic synthesis for constructing complex molecules, especially in medicinal chemistry research aimed at discovering new drugs or optimizing existing ones.
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