(R)-Azetidine-2-carbonitrileoxalate

98%

Reagent Code: #232135
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CAS Number 2173052-89-4

science Other reagents with same CAS 2173052-89-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.14 g/mol
Formula C₆H₈N₂O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its strained azetidine ring and nitrile functionality make it valuable for constructing complex molecules in medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system and metabolic disorder drug research. The oxalate salt form enhances stability and crystallinity, facilitating handling and purification during synthetic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,910.00
inventory 250mg
10-20 days ฿20,440.00
inventory 1g
10-20 days ฿69,170.00
(R)-Azetidine-2-carbonitrileoxalate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its strained azetidine ring and nitrile functionality make it valuable for constructing complex molecules in medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system and metabolic disorder drug research. The oxalate salt form enhances stability a

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its strained azetidine ring and nitrile functionality make it valuable for constructing complex molecules in medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system and metabolic disorder drug research. The oxalate salt form enhances stability and crystallinity, facilitating handling and purification during synthetic processes.

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