(3R)-()-3-(Trifluoroacetamido)pyrrolidine Hydrochloride
≥98%
- Product Code: 70900
CAS:
141043-16-5
| Molecular Weight: | 218.6 g./mol | Molecular Formula: | C₆H₉F₃N₂OHCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02094762 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(3R)-()-3-(Trifluoroacetamido)pyrrolidine Hydrochloride is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic compounds. It serves as a key intermediate in the production of various bioactive molecules, including potential drug candidates targeting neurological disorders and other therapeutic areas. Its chiral structure makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure substances, which are crucial for developing drugs with higher efficacy and fewer side effects. Additionally, this compound is employed in medicinal chemistry for structure-activity relationship (SAR) studies, helping researchers optimize drug potency and selectivity. Its trifluoroacetamido group also contributes to its stability and reactivity, making it a useful building block in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿6,490.00 |
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| 5.000 | 10-20 days | ฿22,780.00 |
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(3R)-()-3-(Trifluoroacetamido)pyrrolidine Hydrochloride
(3R)-()-3-(Trifluoroacetamido)pyrrolidine Hydrochloride is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic compounds. It serves as a key intermediate in the production of various bioactive molecules, including potential drug candidates targeting neurological disorders and other therapeutic areas. Its chiral structure makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure substances, which are crucial for developing drugs with higher efficacy and fewer side effects. Additionally, this compound is employed in medicinal chemistry for structure-activity relationship (SAR) studies, helping researchers optimize drug potency and selectivity. Its trifluoroacetamido group also contributes to its stability and reactivity, making it a useful building block in organic synthesis.
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