4-Nitrobenzyl allyl(1-(3S)-3-methyl-4-[methyl(phenylsulfonyl)amino]-3-phenylbutyl-4-piperidinyl)carbamate

≥95%

Reagent Code: #218752
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CAS Number 502173-16-2

science Other reagents with same CAS 502173-16-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 634.79 g/mol
Formula C₃₄H₄₂N₄O₆S
thermostat Physical Properties
Boiling Point 747.1±70.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.27±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of protease inhibitors, particularly for hepatitis C virus (HCV) treatment. Its structure supports selective binding to enzyme active sites, enhancing drug efficacy. Also employed in the development of targeted therapies due to its ability to modulate biological activity through controlled molecular interactions. Commonly utilized in solid-phase synthesis and combinatorial chemistry for generating bioactive compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1mg
10-20 days ฿17,390.00
5mg
10-20 days ฿52,240.00
4-Nitrobenzyl allyl(1-(3S)-3-methyl-4-[methyl(phenylsulfonyl)amino]-3-phenylbutyl-4-piperidinyl)carbamate
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Used in pharmaceutical research as a key intermediate in the synthesis of protease inhibitors, particularly for hepatitis C virus (HCV) treatment. Its structure supports selective binding to enzyme active sites, enhancing drug efficacy. Also employed in the development of targeted therapies due to its ability to modulate biological activity through controlled molecular interactions. Commonly utilized in solid-phase synthesis and combinatorial chemistry for generating bioactive compounds.

Used in pharmaceutical research as a key intermediate in the synthesis of protease inhibitors, particularly for hepatitis C virus (HCV) treatment. Its structure supports selective binding to enzyme active sites, enhancing drug efficacy. Also employed in the development of targeted therapies due to its ability to modulate biological activity through controlled molecular interactions. Commonly utilized in solid-phase synthesis and combinatorial chemistry for generating bioactive compounds.

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