(S)-(−)-α,α-Diphenyl-2-pyrrolidinemethanol

98%

Reagent Code: #97454
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CAS Number 112068-01-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.34 g/mol
Formula C₁₇H₁₉NO
badge Registry Numbers
MDL Number MFCD00075506
thermostat Physical Properties
Melting Point 77-80 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(S)-(−)-α,α-Diphenyl-2-pyrrolidinemethanol is widely used in asymmetric synthesis as a chiral auxiliary or catalyst. It plays a key role in the production of enantiomerically pure compounds, particularly in pharmaceutical manufacturing, where it helps create drugs with high stereochemical precision. Its application is crucial in the synthesis of complex molecules, such as beta-blockers and other chiral drugs, ensuring enhanced efficacy and reduced side effects. Additionally, it is utilized in academic and industrial research for developing new chiral catalysts and studying stereoselective reactions.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white powder or crystals
Purity 98-100%
Melting Point 76-80
Infrared Spectrum Conforms to Structure
Solubility in Chloroform Almost transparent
Chloroform -69 to -65

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days $345.75
inventory 5g
10-20 days $21.12
inventory 1g
10-20 days $12.93
inventory 25g
10-20 days $93.12
(S)-(−)-α,α-Diphenyl-2-pyrrolidinemethanol
(S)-(−)-α,α-Diphenyl-2-pyrrolidinemethanol is widely used in asymmetric synthesis as a chiral auxiliary or catalyst. It plays a key role in the production of enantiomerically pure compounds, particularly in pharmaceutical manufacturing, where it helps create drugs with high stereochemical precision. Its application is crucial in the synthesis of complex molecules, such as beta-blockers and other chiral drugs, ensuring enhanced efficacy and reduced side effects. Additionally, it is utilized in academic and industrial research for developing new chiral catalysts and studying stereoselective reactions.
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