(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-nitrophenoxy)propanoic acid
95%
- Product Code: 104385
CAS:
99197-78-1
| Molecular Weight: | 326.30 g./mol | Molecular Formula: | C₁₄H₁₈N₂O₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20266848 | |
| Melting Point: | Boiling Point: | 503.6±45.0 °C(Predicted) | |
| Density: | 1.314±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of peptide chemistry. It serves as a building block for the creation of peptide derivatives, where it aids in the introduction of specific functional groups into peptide chains. The compound is also employed in the development of pharmaceuticals, especially in the design of drugs that target specific biological pathways. Its structure allows for selective modifications, making it valuable in the production of biologically active compounds. Additionally, it is used in research laboratories for studying enzyme-substrate interactions and for the development of new therapeutic agents. The presence of the nitro group and the tert-butoxycarbonyl (Boc) protecting group makes it particularly useful in multi-step synthetic processes, where selective deprotection and further functionalization are required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿21,600.00 |
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| 0.250 | 10-20 days | ฿40,500.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-nitrophenoxy)propanoic acid
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of peptide chemistry. It serves as a building block for the creation of peptide derivatives, where it aids in the introduction of specific functional groups into peptide chains. The compound is also employed in the development of pharmaceuticals, especially in the design of drugs that target specific biological pathways. Its structure allows for selective modifications, making it valuable in the production of biologically active compounds. Additionally, it is used in research laboratories for studying enzyme-substrate interactions and for the development of new therapeutic agents. The presence of the nitro group and the tert-butoxycarbonyl (Boc) protecting group makes it particularly useful in multi-step synthetic processes, where selective deprotection and further functionalization are required.
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