tert-Butyl 3-(prop-2-yn-1-yl)azetidine-1-carboxylate
98%
- Product Code: 124152
CAS:
1463502-41-1
| Molecular Weight: | 195.26 g./mol | Molecular Formula: | C₁₁H₁₇NO₂ |
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| EC Number: | MDL Number: | MFCD32173212 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both an azetidine ring and a propargyl group, makes it valuable in the construction of nitrogen-containing heterocycles, which are essential in pharmaceutical research. The tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, enabling further functionalization of the molecule. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, particularly in the fields of medicinal chemistry and drug discovery. Additionally, its alkyne moiety can participate in click chemistry reactions, facilitating the creation of diverse molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,482.00 |
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| 0.250 | 10-20 days | ฿7,623.00 |
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| 1.000 | 10-20 days | ฿20,574.00 |
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tert-Butyl 3-(prop-2-yn-1-yl)azetidine-1-carboxylate
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both an azetidine ring and a propargyl group, makes it valuable in the construction of nitrogen-containing heterocycles, which are essential in pharmaceutical research. The tert-butyloxycarbonyl (Boc) protecting group allows for selective deprotection, enabling further functionalization of the molecule. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, particularly in the fields of medicinal chemistry and drug discovery. Additionally, its alkyne moiety can participate in click chemistry reactions, facilitating the creation of diverse molecular architectures.
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