1-Boc-azetidine-3-carboxylic acid
98%
- Product Code: 105872
CAS:
142253-55-2
| Molecular Weight: | 201.22 g./mol | Molecular Formula: | C₉H₁₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01860897 | |
| Melting Point: | 100.1-101.9°C | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
1-Boc-azetidine-3-carboxylic acid is widely used in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various bioactive compounds and drug candidates. The Boc (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions, making it valuable in peptide synthesis and the development of protease inhibitors. Additionally, it is utilized in the construction of azetidine-containing scaffolds, which are important in medicinal chemistry due to their role in enhancing drug potency and metabolic stability. Its application extends to the synthesis of small molecules targeting neurological disorders, cancer, and infectious diseases.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 98-105 |
| Purity (GC) | 98-100 |
| Purity (Neutralization Titration) | 98-100 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrometry | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £6.56 |
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| 1.000 | 10-20 days | £7.92 |
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| 5.000 | 10-20 days | £26.69 |
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| 25.000 | 10-20 days | £103.13 |
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1-Boc-azetidine-3-carboxylic acid
1-Boc-azetidine-3-carboxylic acid is widely used in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various bioactive compounds and drug candidates. The Boc (tert-butoxycarbonyl) protecting group in the molecule allows for selective reactions, making it valuable in peptide synthesis and the development of protease inhibitors. Additionally, it is utilized in the construction of azetidine-containing scaffolds, which are important in medicinal chemistry due to their role in enhancing drug potency and metabolic stability. Its application extends to the synthesis of small molecules targeting neurological disorders, cancer, and infectious diseases.
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