(R)-1-(3-Pyridylthiocarbamoyl)pyrrolidine-2-carboxylic Acid

≥98%

Reagent Code: #93711
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CAS Number 1443438-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.3 g/mol
Formula C₁₁H₁₃N₃O₂S
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological disorders. Its unique structure allows it to act as a building block for developing inhibitors of specific enzymes or receptors involved in neurodegenerative diseases. Additionally, it is explored in the design of chiral ligands for asymmetric catalysis, aiding in the production of enantiomerically pure drugs. Its application extends to biochemical studies where it is used to investigate protein-ligand interactions and enzyme mechanisms.

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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days £42.97
inventory 25mg
10-20 days £104.68
inventory 100mg
10-20 days £273.80
inventory 500mg
10-20 days £913.97
(R)-1-(3-Pyridylthiocarbamoyl)pyrrolidine-2-carboxylic Acid
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological disorders. Its unique structure allows it to act as a building block for developing inhibitors of specific enzymes or receptors involved in neurodegenerative diseases. Additionally, it is explored in the design of chiral ligands for asymmetric catalysis, aiding in the production of enantiomerically pure drugs. Its application extends to biochemical studies where it is used to investigate protein-ligand interactions and enzyme mechanisms.
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