(2S,4R)-N-(2,6-Dimethylphenyl)-4-hydroxypyrrolidine-2-carboxamide

97%

Reagent Code: #233266
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CAS Number 2227488-62-0

science Other reagents with same CAS 2227488-62-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.29 g/mol
Formula C₁₃H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD33023356
thermostat Physical Properties
Boiling Point 439.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.214±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of antiviral drugs, particularly in the development of protease inhibitors. Its stereochemistry enables selective interactions with biological targets, enhancing drug efficacy. Commonly employed in pharmaceutical research for designing treatments against RNA viruses, including hepatitis C and coronaviruses. The hydroxyl and amide functional groups allow for further chemical modifications, making it valuable in optimizing pharmacokinetic properties of drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,140.00
inventory 250mg
10-20 days ฿7,050.00
inventory 1g
10-20 days ฿19,020.00
(2S,4R)-N-(2,6-Dimethylphenyl)-4-hydroxypyrrolidine-2-carboxamide
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Used as a key intermediate in the synthesis of antiviral drugs, particularly in the development of protease inhibitors. Its stereochemistry enables selective interactions with biological targets, enhancing drug efficacy. Commonly employed in pharmaceutical research for designing treatments against RNA viruses, including hepatitis C and coronaviruses. The hydroxyl and amide functional groups allow for further chemical modifications, making it valuable in optimizing pharmacokinetic properties of drug candi

Used as a key intermediate in the synthesis of antiviral drugs, particularly in the development of protease inhibitors. Its stereochemistry enables selective interactions with biological targets, enhancing drug efficacy. Commonly employed in pharmaceutical research for designing treatments against RNA viruses, including hepatitis C and coronaviruses. The hydroxyl and amide functional groups allow for further chemical modifications, making it valuable in optimizing pharmacokinetic properties of drug candidates.

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