(S)-Bis(4-Methoxyphenyl)(Pyrrolidin-2-Yl)Methanol

97%

Reagent Code: #237167
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CAS Number 131180-57-9

science Other reagents with same CAS 131180-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.39 g/mol
Formula C₁₉H₂₃NO₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Its structure supports asymmetric synthesis, making it valuable in developing drugs with specific stereochemical requirements. Commonly employed in the preparation of protease inhibitors and other biologically active molecules where stereochemistry influences efficacy and safety. Also utilized in research settings for developing novel chiral catalysts and ligands in enantioselective reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,610.00
inventory 1g
10-20 days ฿25,360.00
inventory 5g
10-20 days ฿53,770.00
inventory 250mg
10-20 days ฿12,680.00
(S)-Bis(4-Methoxyphenyl)(Pyrrolidin-2-Yl)Methanol
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Its structure supports asymmetric synthesis, making it valuable in developing drugs with specific stereochemical requirements. Commonly employed in the preparation of protease inhibitors and other biologically active molecules where stereochemistry influences efficacy and safety. Also utilized in research settings for developing novel chir
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Its structure supports asymmetric synthesis, making it valuable in developing drugs with specific stereochemical requirements. Commonly employed in the preparation of protease inhibitors and other biologically active molecules where stereochemistry influences efficacy and safety. Also utilized in research settings for developing novel chiral catalysts and ligands in enantioselective reactions.
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