Potassium (R)-oxirane-2-carboxylate

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Reagent Code: #37781
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CAS Number 82044-23-3

science Other reagents with same CAS 82044-23-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 126.1600 g/mol
Formula C₃H₃KO₃
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MDL Number MFCD00274194
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It serves as a precursor for the synthesis of enantiomerically pure compounds, aiding in the development of drugs with specific stereochemical requirements. Its oxirane (epoxide) functionality makes it valuable in ring-opening reactions, which are crucial for creating complex molecular structures. Additionally, it is employed in the preparation of biologically active molecules, such as beta-blockers and other therapeutic agents, due to its ability to introduce stereocenters efficiently.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,213.00

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Potassium (R)-oxirane-2-carboxylate
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Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It serves as a precursor for the synthesis of enantiomerically pure compounds, aiding in the development of drugs with specific stereochemical requirements. Its oxirane (epoxide) functionality makes it valuable in ring-opening reactions, which are crucial for creating complex molecular structures. Additionally, it is employed in the preparation of biologically active molecules, such

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It serves as a precursor for the synthesis of enantiomerically pure compounds, aiding in the development of drugs with specific stereochemical requirements. Its oxirane (epoxide) functionality makes it valuable in ring-opening reactions, which are crucial for creating complex molecular structures. Additionally, it is employed in the preparation of biologically active molecules, such as beta-blockers and other therapeutic agents, due to its ability to introduce stereocenters efficiently.

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