Methyl(S)-5-oxotetrahydrofuran-2-carboxylate

97%

Reagent Code: #213678
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CAS Number 21461-85-8

science Other reagents with same CAS 21461-85-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.13 g/mol
Formula C₆H₈O₄
badge Registry Numbers
MDL Number MFCD16039325
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the production of renin inhibitors and other cardiovascular drugs. Its cyclic ester structure allows for selective transformations in asymmetric synthesis, making it valuable in developing enantiomerically pure compounds. Commonly employed in multi-step organic syntheses where stereochemistry control is critical. Also utilized in the preparation of gamma-amino acid derivatives and lactone-based bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,100.00
inventory 250mg
10-20 days ฿9,160.00
inventory 5g
10-20 days ฿80,490.00
inventory 1g
10-20 days ฿21,420.00
Methyl(S)-5-oxotetrahydrofuran-2-carboxylate
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Used as a key chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the production of renin inhibitors and other cardiovascular drugs. Its cyclic ester structure allows for selective transformations in asymmetric synthesis, making it valuable in developing enantiomerically pure compounds. Commonly employed in multi-step organic syntheses where stereochemistry control is critical. Also utilized in the preparation of gamma-amino acid derivatives and lactone-based bioact

Used as a key chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the production of renin inhibitors and other cardiovascular drugs. Its cyclic ester structure allows for selective transformations in asymmetric synthesis, making it valuable in developing enantiomerically pure compounds. Commonly employed in multi-step organic syntheses where stereochemistry control is critical. Also utilized in the preparation of gamma-amino acid derivatives and lactone-based bioactive molecules.

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