(S)-Tert-butyl 2-aminopropanoate
95%
- Product Code: 76437
CAS:
21691-50-9
| Molecular Weight: | 145.20 g./mol | Molecular Formula: | C₇H₁₅NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00270591 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, protected from light, stored under inert gas |
Product Description:
(S)-Tert-butyl 2-aminopropanoate is widely used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of optically active compounds. It serves as a key intermediate in the preparation of various active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity.
This compound is also employed in peptide synthesis, where it acts as a protective group for amino acids, ensuring selective reactions during the formation of peptide bonds. Its tert-butyl ester group provides stability under various reaction conditions, making it a valuable tool in organic synthesis.
Additionally, it is utilized in the development of agrochemicals and fine chemicals, where its chiral nature contributes to the creation of more effective and selective products. Its application extends to research and development in asymmetric synthesis, aiding in the discovery of new compounds with potential therapeutic or industrial uses.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,071.00 |
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| 0.250 | 10-20 days | ฿1,602.00 |
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| 1.000 | 10-20 days | ฿4,014.00 |
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(S)-Tert-butyl 2-aminopropanoate
(S)-Tert-butyl 2-aminopropanoate is widely used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of optically active compounds. It serves as a key intermediate in the preparation of various active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity.
This compound is also employed in peptide synthesis, where it acts as a protective group for amino acids, ensuring selective reactions during the formation of peptide bonds. Its tert-butyl ester group provides stability under various reaction conditions, making it a valuable tool in organic synthesis.
Additionally, it is utilized in the development of agrochemicals and fine chemicals, where its chiral nature contributes to the creation of more effective and selective products. Its application extends to research and development in asymmetric synthesis, aiding in the discovery of new compounds with potential therapeutic or industrial uses.
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