N-[(1R,2R)-2-aMino-1,2-bis(4-Methoxyphenyl)ethyl]-4-Methyl-BenzenesulfonaMide

98%

Reagent Code: #70692
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CAS Number 852212-99-8

science Other reagents with same CAS 852212-99-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 426.52854 g/mol
Formula C₂₃H₂₆N₂O₄S
inventory_2 Storage & Handling
Storage 2-8°C, away from light

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both amino and sulfonamide groups, makes it a valuable precursor in the development of pharmaceutical agents, particularly those targeting enzymatic pathways. It is often employed in the design and synthesis of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, its chiral centers allow for the creation of enantiomerically pure substances, which are crucial in drug development to ensure specificity and reduce side effects. Researchers also explore its use in studying molecular interactions and binding affinities due to its unique structural properties.

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Test Parameter Specification
Appearance White Powder
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,690.00
inventory 5g
10-20 days ฿14,880.00
inventory 1g
10-20 days ฿3,100.00

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N-[(1R,2R)-2-aMino-1,2-bis(4-Methoxyphenyl)ethyl]-4-Methyl-BenzenesulfonaMide
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both amino and sulfonamide groups, makes it a valuable precursor in the development of pharmaceutical agents, particularly those targeting enzymatic pathways. It is often employed in the design and synthesis of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, its chiral centers allow for the creation of enantiomerically pure substances, which are crucial in drug development to ensure specificity and reduce side effects. Researchers also explore its use in studying molecular interactions and binding affinities due to its unique structural properties.
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