Ethyl (S)-(-)-1-Ethyl-2-pyrrolidinecarboxylate

≥98%(GC)(T)

Reagent Code: #52525
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CAS Number 938-54-5

science Other reagents with same CAS 938-54-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.24 g/mol
Formula C₉H₁₇NO₂
badge Registry Numbers
MDL Number MFCD00191434
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a precursor for the synthesis of various enantiomerically pure compounds, aiding in the development of drugs with specific stereochemical requirements. Additionally, it is employed in asymmetric catalysis to enhance the efficiency and selectivity of chemical reactions. Its application extends to the preparation of complex molecules in medicinal chemistry, where precise control over stereochemistry is crucial for biological activity.

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inventory 1g
10-20 days ฿3,735.00

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Ethyl (S)-(-)-1-Ethyl-2-pyrrolidinecarboxylate
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Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a precursor for the synthesis of various enantiomerically pure compounds, aiding in the development of drugs with specific stereochemical requirements. Additionally, it is employed in asymmetric catalysis to enhance the efficiency and selectivity of chemical reactions. Its application extends to the preparation of complex molecules in medicinal chemistry, where precise c

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a precursor for the synthesis of various enantiomerically pure compounds, aiding in the development of drugs with specific stereochemical requirements. Additionally, it is employed in asymmetric catalysis to enhance the efficiency and selectivity of chemical reactions. Its application extends to the preparation of complex molecules in medicinal chemistry, where precise control over stereochemistry is crucial for biological activity.

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