tert-butyl 3-(hydroxyimino)azetidine-1-carboxylate
95%
- Product Code: 124593
CAS:
1378674-88-4
| Molecular Weight: | 186.2087 g./mol | Molecular Formula: | C₈H₁₄N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14708204 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the synthesis of compounds with potential biological activity, such as inhibitors or modulators of specific enzymes or receptors. Its structure, featuring a hydroxylimino group and a protected azetidine ring, makes it valuable for constructing nitrogen-containing heterocycles, which are common in drug discovery. Additionally, it is employed in the preparation of peptidomimetics, which mimic peptide structures and are used to design therapeutic agents with enhanced stability and efficacy. Its tert-butyl carboxylate group provides a protective function during synthetic processes, allowing for selective reactions and subsequent deprotection to yield desired products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,510.00 |
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| 1.000 | 10-20 days | ฿7,020.00 |
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| 5.000 | 10-20 days | ฿21,060.00 |
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tert-butyl 3-(hydroxyimino)azetidine-1-carboxylate
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the synthesis of compounds with potential biological activity, such as inhibitors or modulators of specific enzymes or receptors. Its structure, featuring a hydroxylimino group and a protected azetidine ring, makes it valuable for constructing nitrogen-containing heterocycles, which are common in drug discovery. Additionally, it is employed in the preparation of peptidomimetics, which mimic peptide structures and are used to design therapeutic agents with enhanced stability and efficacy. Its tert-butyl carboxylate group provides a protective function during synthetic processes, allowing for selective reactions and subsequent deprotection to yield desired products.
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