(1R,2S)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenyl-1-propanol

98%

Reagent Code: #229834
label
Alias (1R,2S)-2-[N-benzyl-N-(2,4,6-trimethylbenzenesulfonyl)amino]-1-phenyl-1-propanol (1R,2S)-N-benzyl-N-(homotrimethylbenzenesulfonyl)nothephalin
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CAS Number 187324-63-6

science Other reagents with same CAS 187324-63-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 423.57 g/mol
Formula C₂₅H₂₉NO₃S
badge Registry Numbers
EC Number 187324-63-6
MDL Number MFCD02093446
thermostat Physical Properties
Melting Point 130-134 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in the development of enantioselective reactions. Its rigid structure and stereochemical stability make it valuable for controlling the formation of chiral centers in complex organic molecules. Commonly employed in the synthesis of pharmaceutical intermediates where high enantiomeric purity is required. The sulfonamide group facilitates easy removal and modification after stereocontrol has been established, allowing for versatile application in multi-step synthetic routes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿8,910.00
5g
10-20 days ฿31,400.00
(1R,2S)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenyl-1-propanol
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Used as a chiral auxiliary in asymmetric synthesis, particularly in the development of enantioselective reactions. Its rigid structure and stereochemical stability make it valuable for controlling the formation of chiral centers in complex organic molecules. Commonly employed in the synthesis of pharmaceutical intermediates where high enantiomeric purity is required. The sulfonamide group facilitates easy removal and modification after stereocontrol has been established, allowing for versatile application in multi-step synthetic routes.
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