(2S,3R)-1-[(tert-Butoxy)carbonyl]-3-methylazetidine-2-carboxylic acid
95%
- Product Code: 78448
CAS:
1277097-48-9
| Molecular Weight: | 215.3 g./mol | Molecular Formula: | C₁₀H₁₇NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22373926 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid functionality, makes it valuable in peptide and drug development. The Boc group is particularly useful for protecting amines during multi-step synthesis, allowing selective reactions to occur without interference. Additionally, the azetidine ring in its structure is a key motif in medicinal chemistry, often incorporated into drug candidates to enhance their biological activity or improve metabolic stability. This chemical is also employed in the development of protease inhibitors and other therapeutic agents targeting specific enzymes or receptors. Its chiral centers further enable the creation of enantiomerically pure compounds, which are critical in designing drugs with precise activity and reduced side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿21,600.00 |
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| 1.000 | 10-20 days | ฿42,336.00 |
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(2S,3R)-1-[(tert-Butoxy)carbonyl]-3-methylazetidine-2-carboxylic acid
This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid functionality, makes it valuable in peptide and drug development. The Boc group is particularly useful for protecting amines during multi-step synthesis, allowing selective reactions to occur without interference. Additionally, the azetidine ring in its structure is a key motif in medicinal chemistry, often incorporated into drug candidates to enhance their biological activity or improve metabolic stability. This chemical is also employed in the development of protease inhibitors and other therapeutic agents targeting specific enzymes or receptors. Its chiral centers further enable the creation of enantiomerically pure compounds, which are critical in designing drugs with precise activity and reduced side effects.
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