(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-methoxypropanoate
95%
- Product Code: 38093
CAS:
134167-07-0
| Molecular Weight: | 233.2600 g./mol | Molecular Formula: | C₁₀H₁₉NO₅ |
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| EC Number: | MDL Number: | MFCD18837831 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis as a chiral building block for the preparation of various pharmaceuticals and bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxy ester, makes it valuable in peptide synthesis, particularly for introducing chiral centers or specific amino acid derivatives. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization. Additionally, the methoxy ester moiety can be hydrolyzed or transformed into other functional groups, enhancing its versatility in constructing complex molecules. Its application is particularly relevant in the development of drugs targeting neurological disorders, cancer, and infectious diseases, where precise stereochemistry is crucial for efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,455.00 |
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(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-methoxypropanoate
This compound is primarily used in organic synthesis as a chiral building block for the preparation of various pharmaceuticals and bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxy ester, makes it valuable in peptide synthesis, particularly for introducing chiral centers or specific amino acid derivatives. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization. Additionally, the methoxy ester moiety can be hydrolyzed or transformed into other functional groups, enhancing its versatility in constructing complex molecules. Its application is particularly relevant in the development of drugs targeting neurological disorders, cancer, and infectious diseases, where precise stereochemistry is crucial for efficacy.
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