(S)-2-(m-Tolyl)pyrrolidine

98%

Reagent Code: #233462
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CAS Number 1217781-18-4

science Other reagents with same CAS 1217781-18-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.24 g/mol
Formula C₁₁H₁₅N
badge Registry Numbers
MDL Number MFCD06762559
thermostat Physical Properties
Boiling Point 256.7±19.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.975±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and neurodegenerative disease treatments. Its stereochemistry makes it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in the preparation of nootropic and psychotropic compounds due to its structural similarity to known cognitive enhancers. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies involving pyrrolidine-based bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,110.00
inventory 250mg
10-20 days ฿22,210.00

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(S)-2-(m-Tolyl)pyrrolidine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and neurodegenerative disease treatments. Its stereochemistry makes it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in the preparation of nootropic and psychotropic compounds due to its structural similarity to known cognitive enhancers. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) stud
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and neurodegenerative disease treatments. Its stereochemistry makes it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in the preparation of nootropic and psychotropic compounds due to its structural similarity to known cognitive enhancers. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies involving pyrrolidine-based bioactive molecules.
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