(S)-(1-Benzylpyrrolidin-2-yl)diphenylmethanol

97%

Reagent Code: #71076
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CAS Number 118970-95-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.46 g/mol
Formula C₂₄H₂₅NO
badge Registry Numbers
MDL Number MFCD18785744
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description 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.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,742.00
inventory 100mg
10-20 days ฿3,933.00
inventory 250mg
10-20 days ฿5,895.00
(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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