Thiazol-5-ylmethyl ((2S,3S,5S)-5-amino-3-hydroxy-1,6-diphenylhexan-2-yl)carbamate

98%

Reagent Code: #36544
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Alias 利托那韦中间6;N-(5-amino-3-hydroxy-1,6-diphenylhexan-2-yl)carbamic acid 5-thiazolylmethyl ester;Thiazol-5-ylMethyl ((2S,3S,5S)-5-aMino-3-hydroxy-1,6-diphenylhexan-2-yl)carbaMate
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CAS Number 144164-11-4

science Other reagents with same CAS 144164-11-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 425.55 g/mol
Formula C₂₃H₂₇N₃O₃S
badge Registry Numbers
MDL Number MFCD07367634
thermostat Physical Properties
Boiling Point 656.1°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.251±0.06 g/cm3(Predicted)
Storage 2-8°C, inert gas, protected from light

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of potent protease inhibitors. Its structure is particularly valuable in the development of antiviral and antiretroviral drugs, targeting enzymes like HIV protease, which is crucial for the replication of the HIV virus. Additionally, its stereochemistry and functional groups make it a candidate for designing inhibitors that can selectively bind to specific protein targets, offering potential therapeutic applications in treating viral infections and related diseases. Its role in drug development underscores its importance in advancing treatments for complex medical conditions.

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Test Parameter Specification
Appearance White to light-yellow powder or crystals
Purity 97.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,100.00
inventory 250mg
10-20 days ฿2,260.00

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Thiazol-5-ylmethyl ((2S,3S,5S)-5-amino-3-hydroxy-1,6-diphenylhexan-2-yl)carbamate
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of potent protease inhibitors. Its structure is particularly valuable in the development of antiviral and antiretroviral drugs, targeting enzymes like HIV protease, which is crucial for the replication of the HIV virus. Additionally, its stereochemistry and functional groups make it a candidate for designing inhibitors that can selectively bind to specific protein targets, offering potential the

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of potent protease inhibitors. Its structure is particularly valuable in the development of antiviral and antiretroviral drugs, targeting enzymes like HIV protease, which is crucial for the replication of the HIV virus. Additionally, its stereochemistry and functional groups make it a candidate for designing inhibitors that can selectively bind to specific protein targets, offering potential therapeutic applications in treating viral infections and related diseases. Its role in drug development underscores its importance in advancing treatments for complex medical conditions.

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