(S)-3-Hydroxy-4,4-dimethyldihydrofuran-2(3H)-one

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Reagent Code: #234901
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CAS Number 5405-40-3

science Other reagents with same CAS 5405-40-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.14 g/mol
Formula C₆H₁₀O₃
thermostat Physical Properties
Melting Point 90-94°C
Boiling Point 224.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of statins such as rosuvastatin and atorvastatin, which are widely prescribed for lowering cholesterol. Its stereochemistry allows for high selectivity in reactions, making it valuable in asymmetric synthesis. Also employed in the preparation of other bioactive molecules where a chiral lactone structure is required. Its stability and reactivity profile make it suitable for multi-step synthetic routes in fine chemical and drug development industries.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿390.00
inventory 1g
10-20 days ฿2,150.00
inventory 5g
10-20 days ฿6,250.00
inventory 250mg
10-20 days ฿650.00
inventory 25g
10-20 days ฿19,280.00

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(S)-3-Hydroxy-4,4-dimethyldihydrofuran-2(3H)-one
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of statins such as rosuvastatin and atorvastatin, which are widely prescribed for lowering cholesterol. Its stereochemistry allows for high selectivity in reactions, making it valuable in asymmetric synthesis. Also employed in the preparation of other bioactive molecules where a chiral lactone structure is required. Its stability and reactivity profile make it suitable for multi-step synthetic routes in

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of statins such as rosuvastatin and atorvastatin, which are widely prescribed for lowering cholesterol. Its stereochemistry allows for high selectivity in reactions, making it valuable in asymmetric synthesis. Also employed in the preparation of other bioactive molecules where a chiral lactone structure is required. Its stability and reactivity profile make it suitable for multi-step synthetic routes in fine chemical and drug development industries.

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