(R)-2-(Methoxymethyl)pyrrolidine
97%
- Product Code: 60209
Alias:
(R)-(-)-2-(methoxymethyl)pyrrolidine O-methyl-D-prolinol
CAS:
84025-81-0
| Molecular Weight: | 115.17 g./mol | Molecular Formula: | C₆H₁₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00066219 | |
| Melting Point: | Boiling Point: | 61-62°C 40mm | |
| Density: | 0.932 g/mL at 20 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
(R)-2-(Methoxymethyl)pyrrolidine is widely used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various enantiomerically pure compounds, which are essential for developing drugs with high specificity and reduced side effects. This compound is often employed in asymmetric synthesis to create complex molecules with precise stereochemistry. Additionally, it is utilized in the preparation of catalysts and ligands for asymmetric catalytic reactions, enhancing the efficiency and selectivity of these processes. Its role in the synthesis of bioactive molecules and natural products further highlights its importance in medicinal chemistry and drug discovery.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Almost colorless clear liquid |
| PURITYGC | 96.5 % 100 % |
| REFRACTIVE INDEX N20D | 1.445-1.449 |
| Infrared spectrum | Conforms to Structure |
| Specific gravity 2020C | 0.931-0.935 |
| HCL | -33 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $88.90 |
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| 1.000 | 10-20 days | $194.88 |
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| 5.000 | 10-20 days | $892.52 |
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(R)-2-(Methoxymethyl)pyrrolidine
(R)-2-(Methoxymethyl)pyrrolidine is widely used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various enantiomerically pure compounds, which are essential for developing drugs with high specificity and reduced side effects. This compound is often employed in asymmetric synthesis to create complex molecules with precise stereochemistry. Additionally, it is utilized in the preparation of catalysts and ligands for asymmetric catalytic reactions, enhancing the efficiency and selectivity of these processes. Its role in the synthesis of bioactive molecules and natural products further highlights its importance in medicinal chemistry and drug discovery.
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