(R)-1-Benzyl-3-dimethylaminopyrrolidine Dihydrochloride
≥97%
- Product Code: 73157
CAS:
1235058-59-9
Molecular Weight: | 277.23 g./mol | Molecular Formula: | C₁₃H₂₂Cl₂N₂ |
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EC Number: | MDL Number: | MFCD11223480 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a chiral building block or intermediate in the preparation of various pharmacologically active molecules. Its structure, featuring a benzyl group and a dimethylamino moiety, makes it valuable for the development of compounds targeting specific biological pathways, particularly in the synthesis of ligands for receptors or enzymes. Additionally, it is employed in asymmetric synthesis to induce chirality in the production of enantiomerically pure substances, which are crucial in the development of drugs with high specificity and reduced side effects. Its dihydrochloride form enhances solubility, facilitating its use in aqueous reaction conditions.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | £325.23 |
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25.000 | 10-20 days | £1,183.55 |
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(R)-1-Benzyl-3-dimethylaminopyrrolidine Dihydrochloride
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a chiral building block or intermediate in the preparation of various pharmacologically active molecules. Its structure, featuring a benzyl group and a dimethylamino moiety, makes it valuable for the development of compounds targeting specific biological pathways, particularly in the synthesis of ligands for receptors or enzymes. Additionally, it is employed in asymmetric synthesis to induce chirality in the production of enantiomerically pure substances, which are crucial in the development of drugs with high specificity and reduced side effects. Its dihydrochloride form enhances solubility, facilitating its use in aqueous reaction conditions.
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