2-((tert-Butoxycarbonyl)amino)-2-(o-tolyl)acetic acid
95%
- Product Code: 58250
CAS:
40512-48-9
| Molecular Weight: | 265.31 g./mol | Molecular Formula: | C₁₄H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03789594 | |
| Melting Point: | Boiling Point: | 423.6±40.0 °C(Predicted) | |
| Density: | 1.159±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the preparation of peptides and other biologically active compounds. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during chemical reactions. This protection is crucial in multi-step synthesis processes, allowing selective reactions at other sites of the molecule. Additionally, it is employed in the development of pharmaceuticals, where its structural features contribute to the creation of drug candidates with specific therapeutic properties. Its application extends to research laboratories focused on medicinal chemistry, where it aids in the study and modification of molecular structures to enhance drug efficacy and stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £152.66 |
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| 0.250 | 10-20 days | £244.26 |
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| 1.000 | 10-20 days | £430.31 |
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2-((tert-Butoxycarbonyl)amino)-2-(o-tolyl)acetic acid
This chemical is primarily used in organic synthesis, particularly in the preparation of peptides and other biologically active compounds. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during chemical reactions. This protection is crucial in multi-step synthesis processes, allowing selective reactions at other sites of the molecule. Additionally, it is employed in the development of pharmaceuticals, where its structural features contribute to the creation of drug candidates with specific therapeutic properties. Its application extends to research laboratories focused on medicinal chemistry, where it aids in the study and modification of molecular structures to enhance drug efficacy and stability.
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