(2S,4S)-4-Nitrobenzyl 4-(acetylthio)-2-(((tert-butoxycarbonyl)(sulfamoyl)amino)methyl)pyrrolidine-1-carboxylate

98%

Reagent Code: #52972
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CAS Number 491878-06-9

science Other reagents with same CAS 491878-06-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 532.59 g/mol
Formula C₂₀H₂₈N₄O₉S₂
thermostat Physical Properties
Melting Point 124-132°C
Boiling Point 686.8°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of protease inhibitors. Its structure is designed to interact with specific enzyme active sites, making it valuable in the design of therapeutic agents targeting diseases such as HIV and hepatitis C. The inclusion of functional groups like the nitrobenzyl ester and acetylthio moiety allows for controlled release and targeted delivery mechanisms, enhancing the efficacy of the drug candidates. Additionally, its tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, enabling precise modifications to the molecule. This compound is also explored in research for its potential in creating prodrugs, which can improve bioavailability and reduce side effects in therapeutic applications.

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Test Parameter Specification
Appearance White to pale yellow solid
Purity 97.5-100
Melting Point 129-136
Loss on Drying 2.0

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,060.00
inventory 5g
10-20 days ฿3,033.00
inventory 250mg
10-20 days ฿400.00

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(2S,4S)-4-Nitrobenzyl 4-(acetylthio)-2-(((tert-butoxycarbonyl)(sulfamoyl)amino)methyl)pyrrolidine-1-carboxylate
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This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of protease inhibitors. Its structure is designed to interact with specific enzyme active sites, making it valuable in the design of therapeutic agents targeting diseases such as HIV and hepatitis C. The inclusion of functional groups like the nitrobenzyl ester and acetylthio moiety allows for controlled release and targeted delivery mechanisms, enhancing the efficacy of the drug ca

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of protease inhibitors. Its structure is designed to interact with specific enzyme active sites, making it valuable in the design of therapeutic agents targeting diseases such as HIV and hepatitis C. The inclusion of functional groups like the nitrobenzyl ester and acetylthio moiety allows for controlled release and targeted delivery mechanisms, enhancing the efficacy of the drug candidates. Additionally, its tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, enabling precise modifications to the molecule. This compound is also explored in research for its potential in creating prodrugs, which can improve bioavailability and reduce side effects in therapeutic applications.

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