(3R,5S)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)pyrrolidin-3-ol

95%

Reagent Code: #230904
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CAS Number 151953-64-9

science Other reagents with same CAS 151953-64-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 419.51 g/mol
Formula C₂₆H₂₉NO₄
badge Registry Numbers
MDL Number MFCD29918292
thermostat Physical Properties
Boiling Point 569.4±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.160±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of certain pharmaceuticals, particularly in the production of complex molecules requiring high enantiomeric purity. Its structural features make it valuable in asymmetric synthesis, where precise stereochemistry is critical. Commonly employed in the development of protease inhibitors and other bioactive compounds, especially in research settings focused on antiviral and cardiovascular agents. The compound’s hydroxyl and protected alcohol functionalities allow for selective modifications, enabling stepwise construction of intricate molecular architectures in drug discovery and process chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,190.00
250mg
10-20 days ฿7,160.00
5g
10-20 days ฿24,830.00
25g
10-20 days ฿75,240.00
1g
10-20 days ฿15,790.00
(3R,5S)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)pyrrolidin-3-ol
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Used as a key chiral intermediate in the synthesis of certain pharmaceuticals, particularly in the production of complex molecules requiring high enantiomeric purity. Its structural features make it valuable in asymmetric synthesis, where precise stereochemistry is critical. Commonly employed in the development of protease inhibitors and other bioactive compounds, especially in research settings focused on antiviral and cardiovascular agents. The compound’s hydroxyl and protected alcohol functionalities

Used as a key chiral intermediate in the synthesis of certain pharmaceuticals, particularly in the production of complex molecules requiring high enantiomeric purity. Its structural features make it valuable in asymmetric synthesis, where precise stereochemistry is critical. Commonly employed in the development of protease inhibitors and other bioactive compounds, especially in research settings focused on antiviral and cardiovascular agents. The compound’s hydroxyl and protected alcohol functionalities allow for selective modifications, enabling stepwise construction of intricate molecular architectures in drug discovery and process chemistry.

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