tert-Butyl ((S)-1-(((S)-1-cyclohexyl-2-((S)-2-(4-(3-hydroxybenzoyl)thiazol-2-yl)pyrrolidin-1-yl)-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

97%

Reagent Code: #233400
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CAS Number 2095244-42-9

science Other reagents with same CAS 2095244-42-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 598.75 g/mol
Formula C₃₁H₄₂N₄O₆S
badge Registry Numbers
MDL Number MFCD32215338
thermostat Physical Properties
Boiling Point 805.4±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.245±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in pharmaceutical synthesis as an intermediate for protease inhibitors, particularly in the development of antiviral drugs. Its chiral structure with multiple stereocenters supports high selectivity in biological targeting, making it valuable in creating active pharmaceutical ingredients (APIs) for treatments involving enzyme regulation, such as antiviral therapies for chronic infections or oncology applications. The tert-butyl carbamate group functions as a protecting group during synthesis, enabling efficient control of bond formation and easy removal to activate the core structure. Commonly employed in research settings for optimizing drug potency and metabolic stability.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿17,580.00
inventory 100mg
10-20 days ฿50,730.00

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tert-Butyl ((S)-1-(((S)-1-cyclohexyl-2-((S)-2-(4-(3-hydroxybenzoyl)thiazol-2-yl)pyrrolidin-1-yl)-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate
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Used in pharmaceutical synthesis as an intermediate for protease inhibitors, particularly in the development of antiviral drugs. Its chiral structure with multiple stereocenters supports high selectivity in biological targeting, making it valuable in creating active pharmaceutical ingredients (APIs) for treatments involving enzyme regulation, such as antiviral therapies for chronic infections or oncology applications. The tert-butyl carbamate group functions as a protecting group during synthesis, enabli

Used in pharmaceutical synthesis as an intermediate for protease inhibitors, particularly in the development of antiviral drugs. Its chiral structure with multiple stereocenters supports high selectivity in biological targeting, making it valuable in creating active pharmaceutical ingredients (APIs) for treatments involving enzyme regulation, such as antiviral therapies for chronic infections or oncology applications. The tert-butyl carbamate group functions as a protecting group during synthesis, enabling efficient control of bond formation and easy removal to activate the core structure. Commonly employed in research settings for optimizing drug potency and metabolic stability.

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