(S)-tert-Butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate
≥95%
- Product Code: 71108
CAS:
191231-58-0
| Molecular Weight: | 214.31 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD07786221 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a pyrrolidine ring and a tert-butyl carboxylate group, makes it a valuable building block for the development of chiral compounds, particularly in the production of drugs targeting neurological and cardiovascular disorders. Additionally, it is employed in the creation of ligands for asymmetric catalysis, aiding in the efficient synthesis of enantiomerically pure substances. Its application extends to research settings, where it is used to explore new chemical reactions and pathways in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $365.19 |
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| 0.250 | 10-20 days | $586.25 |
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| 1.000 | 10-20 days | $1,470.07 |
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(S)-tert-Butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a pyrrolidine ring and a tert-butyl carboxylate group, makes it a valuable building block for the development of chiral compounds, particularly in the production of drugs targeting neurological and cardiovascular disorders. Additionally, it is employed in the creation of ligands for asymmetric catalysis, aiding in the efficient synthesis of enantiomerically pure substances. Its application extends to research settings, where it is used to explore new chemical reactions and pathways in organic synthesis.
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