(S)-1-Boc-3-(Bromomethyl)pyrrolidine
98%
- Product Code: 121416
CAS:
1067230-64-1
| Molecular Weight: | 264.16 g./mol | Molecular Formula: | C₁₀H₁₈BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08059334 | |
| Melting Point: | Boiling Point: | 300.053 °C at 760 mmHg | |
| Density: | 1.313 g/cm3 | Storage Condition: | 2-8°C, inert gas |
Product Description:
This chemical is widely used as a key intermediate in organic synthesis, particularly in the production of pharmaceuticals. It plays a crucial role in the development of active pharmaceutical ingredients (APIs) for various therapeutic agents. Its structure, featuring a Boc-protected amine and a bromomethyl group, allows for selective functionalization, making it valuable in constructing complex molecules. It is often employed in the synthesis of pyrrolidine-based compounds, which are common in drugs targeting neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it serves as a building block in peptide chemistry and in the preparation of chiral compounds, leveraging its stereocenter for enantioselective synthesis. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,844.00 |
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| 0.250 | 10-20 days | ฿6,219.00 |
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| 1.000 | 10-20 days | ฿18,513.00 |
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(S)-1-Boc-3-(Bromomethyl)pyrrolidine
This chemical is widely used as a key intermediate in organic synthesis, particularly in the production of pharmaceuticals. It plays a crucial role in the development of active pharmaceutical ingredients (APIs) for various therapeutic agents. Its structure, featuring a Boc-protected amine and a bromomethyl group, allows for selective functionalization, making it valuable in constructing complex molecules. It is often employed in the synthesis of pyrrolidine-based compounds, which are common in drugs targeting neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it serves as a building block in peptide chemistry and in the preparation of chiral compounds, leveraging its stereocenter for enantioselective synthesis. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry and drug discovery.
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