(S)-Methyl 2-((tert-butoxycarbonyl)amino)pent-4-ynoate
95%
- Product Code: 53270
CAS:
71460-02-1
| Molecular Weight: | 227.2570 g./mol | Molecular Formula: | C₁₁H₁₇NO₄ |
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| EC Number: | MDL Number: | MFCD07368399 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a building block in the synthesis of chiral compounds, where its structure allows for the introduction of specific functional groups. The tert-butoxycarbonyl (Boc) protecting group is particularly useful in peptide synthesis, as it safeguards the amino group during reactions and can be selectively removed later. The alkyne moiety in the molecule offers versatility for click chemistry applications, enabling the formation of triazoles or other cycloaddition products. This makes it valuable in drug discovery, material science, and bioconjugation studies. Additionally, its chiral center is significant in the production of enantiomerically pure compounds, which are critical in the development of active pharmaceutical ingredients (APIs) with specific biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,944.00 |
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(S)-Methyl 2-((tert-butoxycarbonyl)amino)pent-4-ynoate
This compound is primarily used in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a building block in the synthesis of chiral compounds, where its structure allows for the introduction of specific functional groups. The tert-butoxycarbonyl (Boc) protecting group is particularly useful in peptide synthesis, as it safeguards the amino group during reactions and can be selectively removed later. The alkyne moiety in the molecule offers versatility for click chemistry applications, enabling the formation of triazoles or other cycloaddition products. This makes it valuable in drug discovery, material science, and bioconjugation studies. Additionally, its chiral center is significant in the production of enantiomerically pure compounds, which are critical in the development of active pharmaceutical ingredients (APIs) with specific biological activities.
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