(S)-(1-Benzylpyrrolidin-2-yl)diphenylmethanol
97%
- Product Code: 71076
CAS:
118970-95-9
| Molecular Weight: | 343.46 g./mol | Molecular Formula: | C₂₄H₂₅NO |
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| EC Number: | MDL Number: | MFCD18785744 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a chiral intermediate or building block in the synthesis of various pharmacologically active molecules. Its structure, featuring a diphenylmethanol group and a benzyl-substituted pyrrolidine ring, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the development of drugs targeting the central nervous system, particularly those interacting with neurotransmitter receptors. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for optimizing drug efficacy and reducing side effects. Researchers also explore its potential in asymmetric synthesis, where it serves as a ligand or catalyst in stereoselective reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | ฿3,933.00 |
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| 0.250 | 10-20 days | ฿5,895.00 |
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| 1.000 | 10-20 days | ฿14,742.00 |
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(S)-(1-Benzylpyrrolidin-2-yl)diphenylmethanol
This compound is primarily utilized in the field of medicinal chemistry as a chiral intermediate or building block in the synthesis of various pharmacologically active molecules. Its structure, featuring a diphenylmethanol group and a benzyl-substituted pyrrolidine ring, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the development of drugs targeting the central nervous system, particularly those interacting with neurotransmitter receptors. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for optimizing drug efficacy and reducing side effects. Researchers also explore its potential in asymmetric synthesis, where it serves as a ligand or catalyst in stereoselective reactions.
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