(R)-2-Methylpyrrolidine hydrochloride
97%
- Product Code: 229938
Alias:
(R)-2-methylpyrrolidine hydrochloride
CAS:
135324-85-5
| Molecular Weight: | 121.61 g./mol | Molecular Formula: | C₅H₁₂ClN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06796610 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients where stereochemistry plays a critical role in biological activity. Commonly employed in the development of central nervous system agents, including antidepressants and antipsychotics, due to its structural similarity to natural neurotransmitters. Also utilized in agrochemicals for the creation of enantiomerically pure pesticides and herbicides, improving efficacy and reducing environmental impact. Serves as a resolving agent or intermediate in asymmetric synthesis, enabling the selective formation of one enantiomer over another. Its hydrochloride salt form enhances stability and solubility, facilitating handling and integration into multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.200 | 10-20 days | $9.37 |
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| 5.000 | 10-20 days | $122.81 |
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| 25.000 | 10-20 days | $594.30 |
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| 100.000 | 10-20 days | $1,982.20 |
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| 1.000 | 10-20 days | $29.14 |
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(R)-2-Methylpyrrolidine hydrochloride
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients where stereochemistry plays a critical role in biological activity. Commonly employed in the development of central nervous system agents, including antidepressants and antipsychotics, due to its structural similarity to natural neurotransmitters. Also utilized in agrochemicals for the creation of enantiomerically pure pesticides and herbicides, improving efficacy and reducing environmental impact. Serves as a resolving agent or intermediate in asymmetric synthesis, enabling the selective formation of one enantiomer over another. Its hydrochloride salt form enhances stability and solubility, facilitating handling and integration into multi-step synthetic routes.
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| Stable in pH range | - |
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