N-((1S,2S)-2-Amino-1,2-bis(4-methoxyphenyl)ethyl)-4-methylbenzenesulfonamide

97%

Reagent Code: #50146
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CAS Number 887924-07-4

science Other reagents with same CAS 887924-07-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 426.53 g/mol
Formula C₂₃H₂₆N₂O₄S
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Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. Its structure, featuring both sulfonamide and amino groups, makes it a valuable building block for developing potential therapeutic agents. Researchers often explore its use in designing inhibitors for specific enzymes or receptors, particularly in the context of anti-inflammatory or anticancer drug development. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, which can be crucial for optimizing biological activity and reducing side effects in drug candidates.

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Test Parameter Specification
Appearance White to Off-White to Pale Yellow Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿864.00

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N-((1S,2S)-2-Amino-1,2-bis(4-methoxyphenyl)ethyl)-4-methylbenzenesulfonamide
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This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. Its structure, featuring both sulfonamide and amino groups, makes it a valuable building block for developing potential therapeutic agents. Researchers often explore its use in designing inhibitors for specific enzymes or receptors, particularly in the context of anti-inflammatory or anticancer drug development. Additionally, its chiral centers allow for the creation of e

This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. Its structure, featuring both sulfonamide and amino groups, makes it a valuable building block for developing potential therapeutic agents. Researchers often explore its use in designing inhibitors for specific enzymes or receptors, particularly in the context of anti-inflammatory or anticancer drug development. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, which can be crucial for optimizing biological activity and reducing side effects in drug candidates.

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