(S)-N-Benzyl-3-methylaminopyrrolidine
>98%(GC)
- Product Code: 69108
CAS:
169749-99-9
| Molecular Weight: | 190.28 g./mol | Molecular Formula: | C₁₂H₁₈N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191310 | |
| Melting Point: | Boiling Point: | ||
| Density: | 0.990(lit.) | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a chiral building block for the synthesis of various pharmaceutical agents. Its structure, featuring a pyrrolidine ring and a benzyl group, makes it a valuable intermediate in the development of drugs targeting the central nervous system, particularly those acting on neurotransmitter receptors. It is often employed in the preparation of compounds with potential applications in treating neurological disorders such as depression, anxiety, and schizophrenia. Additionally, its stereochemistry allows for the creation of enantiomerically pure drugs, enhancing specificity and reducing side effects. Researchers also explore its use in the design of ligands for asymmetric catalysis, contributing to the synthesis of complex organic molecules with high enantioselectivity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Almost colorless clear liquid |
| PURITY | 97.5-100 |
| Specific rotation 20DC10 EtOH | 2.8-+3.2 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,700.00 |
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| 5.000 | 10-20 days | ฿10,200.00 |
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(S)-N-Benzyl-3-methylaminopyrrolidine
This compound is primarily utilized in the field of medicinal chemistry as a chiral building block for the synthesis of various pharmaceutical agents. Its structure, featuring a pyrrolidine ring and a benzyl group, makes it a valuable intermediate in the development of drugs targeting the central nervous system, particularly those acting on neurotransmitter receptors. It is often employed in the preparation of compounds with potential applications in treating neurological disorders such as depression, anxiety, and schizophrenia. Additionally, its stereochemistry allows for the creation of enantiomerically pure drugs, enhancing specificity and reducing side effects. Researchers also explore its use in the design of ligands for asymmetric catalysis, contributing to the synthesis of complex organic molecules with high enantioselectivity.
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