(3R,4R)-1-Benzyl-4-hydroxy-3-pyrrolidinemethanol

≥96%(GC)

Reagent Code: #57328
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CAS Number 253129-03-2

science Other reagents with same CAS 253129-03-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.27 g/mol
Formula C₁₂H₁₇NO₂
badge Registry Numbers
MDL Number MFCD10567193
thermostat Physical Properties
Melting Point 70°C
inventory_2 Storage & Handling
Storage Room temperature, dry, inert gas storage

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a benzyl group and hydroxyl functionality, makes it a valuable building block for creating complex molecules with specific stereochemistry.

In medicinal chemistry, it is often employed in the production of inhibitors or modulators targeting enzymes or receptors. Its chiral centers allow for the creation of enantiomerically pure compounds, which is crucial for achieving desired biological activity and minimizing side effects in drug candidates.

Additionally, it finds application in the synthesis of bioactive alkaloids and other natural product derivatives, contributing to the exploration of new therapeutic agents. Its versatility in organic synthesis also extends to the preparation of ligands for asymmetric catalysis, enhancing the efficiency of chemical transformations in drug manufacturing processes.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White - slightly pale reddish yellow crystal - powder
Purity 95.5-100
Specific rotation [α]20/D (c=1, methanol) +28 to +37
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,000.00
inventory 250mg
10-20 days ฿19,260.00

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(3R,4R)-1-Benzyl-4-hydroxy-3-pyrrolidinemethanol
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a benzyl group and hydroxyl functionality, makes it a valuable building block for creating complex molecules with specific stereochemistry.

In medicinal chemistry, it is often employed in the production of inhibitors or modulators targeting enzymes or receptors. Its chiral centers allow for the creation of enantiomerically pure compounds, wh

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its structure, featuring a benzyl group and hydroxyl functionality, makes it a valuable building block for creating complex molecules with specific stereochemistry.

In medicinal chemistry, it is often employed in the production of inhibitors or modulators targeting enzymes or receptors. Its chiral centers allow for the creation of enantiomerically pure compounds, which is crucial for achieving desired biological activity and minimizing side effects in drug candidates.

Additionally, it finds application in the synthesis of bioactive alkaloids and other natural product derivatives, contributing to the exploration of new therapeutic agents. Its versatility in organic synthesis also extends to the preparation of ligands for asymmetric catalysis, enhancing the efficiency of chemical transformations in drug manufacturing processes.

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