trans-tert-Butyl 3-(Hydroxymethyl)-4-methylpyrrolidine-1-carboxylate
97%
- Product Code: 71318
CAS:
1349715-96-3
| Molecular Weight: | 215.29 g./mol | Molecular Formula: | C₁₁H₂₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179042 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a pyrrolidine ring with hydroxyl and carboxylate groups, makes it a versatile building block for the development of bioactive compounds. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cardiovascular disorders. Additionally, its tert-butyl group provides steric protection, enhancing selectivity in chemical reactions. This compound is also used in the preparation of chiral ligands for asymmetric catalysis, aiding in the creation of enantiomerically pure substances.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿7,686.00 |
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| 1.000 | 10-20 days | ฿19,206.00 |
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trans-tert-Butyl 3-(Hydroxymethyl)-4-methylpyrrolidine-1-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a pyrrolidine ring with hydroxyl and carboxylate groups, makes it a versatile building block for the development of bioactive compounds. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or cardiovascular disorders. Additionally, its tert-butyl group provides steric protection, enhancing selectivity in chemical reactions. This compound is also used in the preparation of chiral ligands for asymmetric catalysis, aiding in the creation of enantiomerically pure substances.
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