(S)-2-(4-Methylphenylsulfonamido)propanoic acid

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Reagent Code: #51147
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CAS Number 21957-58-4

science Other reagents with same CAS 21957-58-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.28 g/mol
Formula C₁₀H₁₃NO₄S
badge Registry Numbers
MDL Number MFCD02259513
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily utilized in the pharmaceutical and biochemical research fields. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzyme inhibition. Its structure, featuring a sulfonamide group, makes it valuable in designing drugs that interact with specific proteins or enzymes, often in the context of anti-inflammatory or antimicrobial applications. Researchers also explore its potential in chiral synthesis due to its stereochemistry, which is crucial for producing enantiomerically pure substances. Additionally, it may be used in studies related to metabolic pathways or as a reference standard in analytical chemistry for method development and validation.

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Test Parameter Specification
Appearance Off-white to pink solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿350.00
inventory 250mg
10-20 days ฿290.00
inventory 5g
10-20 days ฿940.00

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(S)-2-(4-Methylphenylsulfonamido)propanoic acid
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This chemical is primarily utilized in the pharmaceutical and biochemical research fields. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzyme inhibition. Its structure, featuring a sulfonamide group, makes it valuable in designing drugs that interact with specific proteins or enzymes, often in the context of anti-inflammatory or antimicrobial applications. Researchers also explore its potential in chiral synthesis due to its ster

This chemical is primarily utilized in the pharmaceutical and biochemical research fields. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzyme inhibition. Its structure, featuring a sulfonamide group, makes it valuable in designing drugs that interact with specific proteins or enzymes, often in the context of anti-inflammatory or antimicrobial applications. Researchers also explore its potential in chiral synthesis due to its stereochemistry, which is crucial for producing enantiomerically pure substances. Additionally, it may be used in studies related to metabolic pathways or as a reference standard in analytical chemistry for method development and validation.

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