(S)-4-((tert-Butoxycarbonyl)amino)-4-phenylbutanoic acid
97%
- Product Code: 38492
CAS:
175224-99-4
| Molecular Weight: | 279.3315 g./mol | Molecular Formula: | C₁₅H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17214545 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of peptides and other biologically active molecules. It serves as a key intermediate in the production of chiral compounds, particularly in the pharmaceutical industry, where it is used to create drugs with specific stereochemical requirements. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino group during synthetic processes, allowing for selective reactions to occur without interference. Its application is particularly significant in the development of therapeutic agents targeting neurological and metabolic disorders, where precise molecular configurations are essential for efficacy. Additionally, it is employed in research settings for studying enzyme mechanisms and designing inhibitors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,343.00 |
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(S)-4-((tert-Butoxycarbonyl)amino)-4-phenylbutanoic acid
This compound is primarily utilized in the synthesis of peptides and other biologically active molecules. It serves as a key intermediate in the production of chiral compounds, particularly in the pharmaceutical industry, where it is used to create drugs with specific stereochemical requirements. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino group during synthetic processes, allowing for selective reactions to occur without interference. Its application is particularly significant in the development of therapeutic agents targeting neurological and metabolic disorders, where precise molecular configurations are essential for efficacy. Additionally, it is employed in research settings for studying enzyme mechanisms and designing inhibitors.
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