(2R,4S)-Benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate

95%

Reagent Code: #36496
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CAS Number 1448706-36-2

science Other reagents with same CAS 1448706-36-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.2800 g/mol
Formula C₁₃H₁₇NO₄
badge Registry Numbers
MDL Number MFCD09998723
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex drug molecules. Its structure, featuring both hydroxyl and carboxylate functional groups, makes it a valuable building block in medicinal chemistry. It is often employed in the development of antiviral and anticancer agents, where its stereochemistry plays a critical role in enhancing the efficacy and specificity of the final drug product. Additionally, it is used in research settings for the preparation of chiral compounds, aiding in the study of stereoselective reactions and drug-target interactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,100.00
inventory 250mg
10-20 days ฿8,120.00
inventory 1g
10-20 days ฿14,980.00
inventory 10g
10-20 days ฿79,420.00
inventory 5g
10-20 days ฿45,820.00

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(2R,4S)-Benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex drug molecules. Its structure, featuring both hydroxyl and carboxylate functional groups, makes it a valuable building block in medicinal chemistry. It is often employed in the development of antiviral and anticancer agents, where its stereochemistry plays a critical role in enhancing the efficacy and specificity of the final drug product. Additionally, it is used in resea

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of complex drug molecules. Its structure, featuring both hydroxyl and carboxylate functional groups, makes it a valuable building block in medicinal chemistry. It is often employed in the development of antiviral and anticancer agents, where its stereochemistry plays a critical role in enhancing the efficacy and specificity of the final drug product. Additionally, it is used in research settings for the preparation of chiral compounds, aiding in the study of stereoselective reactions and drug-target interactions.

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