(R)-5-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid
98%
- Product Code: 37696
CAS:
128135-39-7
| Molecular Weight: | 303.3514 g./mol | Molecular Formula: | C₁₄H₂₅NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32068492 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the preparation of peptides and other biologically active molecules. It serves as a key intermediate in the development of protected amino acid derivatives, which are essential for constructing complex peptide chains with high precision. Its tert-butoxy and tert-butoxycarbonyl groups act as protective groups, ensuring that specific functional groups remain intact during synthetic processes. This chemical is also employed in pharmaceutical research for the synthesis of drug candidates, enabling the study of their therapeutic potential. Additionally, it finds application in the production of chiral compounds, leveraging its stereochemistry to achieve desired enantiomeric purity in final products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,728.00 |
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(R)-5-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid
This compound is primarily utilized in the field of organic synthesis, particularly in the preparation of peptides and other biologically active molecules. It serves as a key intermediate in the development of protected amino acid derivatives, which are essential for constructing complex peptide chains with high precision. Its tert-butoxy and tert-butoxycarbonyl groups act as protective groups, ensuring that specific functional groups remain intact during synthetic processes. This chemical is also employed in pharmaceutical research for the synthesis of drug candidates, enabling the study of their therapeutic potential. Additionally, it finds application in the production of chiral compounds, leveraging its stereochemistry to achieve desired enantiomeric purity in final products.
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