(S)-2-(((Benzyloxy)carbonyl)amino)-3-(1-(2,4-dinitrophenyl)-1H-imidazol-4-yl)propanoic acid

95%

Reagent Code: #38061
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CAS Number 63013-46-7

science Other reagents with same CAS 63013-46-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 455.38 g/mol
Formula C₂₀H₁₇N₅O₈
badge Registry Numbers
MDL Number MFCD20264817
thermostat Physical Properties
Boiling Point 739.2±60.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in biochemical research as a specialized reagent for studying enzyme activity and protein interactions. Its structure, featuring a benzyloxycarbonyl protecting group and a dinitrophenyl moiety, makes it particularly useful in peptide synthesis and as a substrate for proteolytic enzymes. Researchers employ it to investigate the specificity and kinetics of enzymes like proteases, which are critical in understanding cellular processes and developing therapeutic agents. Additionally, its unique design allows for the detection and quantification of enzyme activity through spectrophotometric methods, leveraging the distinct absorbance properties of the dinitrophenyl group. This chemical is also valuable in the development of enzyme inhibitors, aiding in the discovery of drugs targeting specific enzymatic pathways in diseases such as cancer and inflammatory disorders.

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Test Parameter Specification
Appearance Solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,130.00
inventory 250mg
10-20 days ฿7,960.00

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(S)-2-(((Benzyloxy)carbonyl)amino)-3-(1-(2,4-dinitrophenyl)-1H-imidazol-4-yl)propanoic acid
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This compound is primarily utilized in biochemical research as a specialized reagent for studying enzyme activity and protein interactions. Its structure, featuring a benzyloxycarbonyl protecting group and a dinitrophenyl moiety, makes it particularly useful in peptide synthesis and as a substrate for proteolytic enzymes. Researchers employ it to investigate the specificity and kinetics of enzymes like proteases, which are critical in understanding cellular processes and developing therapeutic agents. Ad

This compound is primarily utilized in biochemical research as a specialized reagent for studying enzyme activity and protein interactions. Its structure, featuring a benzyloxycarbonyl protecting group and a dinitrophenyl moiety, makes it particularly useful in peptide synthesis and as a substrate for proteolytic enzymes. Researchers employ it to investigate the specificity and kinetics of enzymes like proteases, which are critical in understanding cellular processes and developing therapeutic agents. Additionally, its unique design allows for the detection and quantification of enzyme activity through spectrophotometric methods, leveraging the distinct absorbance properties of the dinitrophenyl group. This chemical is also valuable in the development of enzyme inhibitors, aiding in the discovery of drugs targeting specific enzymatic pathways in diseases such as cancer and inflammatory disorders.

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