trans-2-(2-Methoxyphenyl)-5-oxotetrahydrofuran-3-carboxylic acid

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Reagent Code: #208660
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CAS Number 99226-02-5

science Other reagents with same CAS 99226-02-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.22 g/mol
Formula C₁₂H₁₂O₅
badge Registry Numbers
MDL Number MFCD09749700
thermostat Physical Properties
Boiling Point 479.1±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of anticoagulant pharmaceuticals, particularly in the preparation of factor Xa inhibitors. Its chiral structure and functional groups allow for selective reactions in multi-step drug manufacturing processes. Commonly employed in research and development of novel cardiovascular medications due to its ability to enhance metabolic stability and binding affinity in active compounds. Also utilized in asymmetric synthesis to produce enantiomerically pure drugs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿330.00
inventory 5g
10-20 days ฿1,240.00
inventory 10g
10-20 days ฿1,960.00

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trans-2-(2-Methoxyphenyl)-5-oxotetrahydrofuran-3-carboxylic acid
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Used as a key intermediate in the synthesis of anticoagulant pharmaceuticals, particularly in the preparation of factor Xa inhibitors. Its chiral structure and functional groups allow for selective reactions in multi-step drug manufacturing processes. Commonly employed in research and development of novel cardiovascular medications due to its ability to enhance metabolic stability and binding affinity in active compounds. Also utilized in asymmetric synthesis to produce enantiomerically pure drugs.

Used as a key intermediate in the synthesis of anticoagulant pharmaceuticals, particularly in the preparation of factor Xa inhibitors. Its chiral structure and functional groups allow for selective reactions in multi-step drug manufacturing processes. Commonly employed in research and development of novel cardiovascular medications due to its ability to enhance metabolic stability and binding affinity in active compounds. Also utilized in asymmetric synthesis to produce enantiomerically pure drugs.

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