tert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoate

≥95%

Reagent Code: #172012
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CAS Number 125988-01-4

science Other reagents with same CAS 125988-01-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.26 g/mol
Formula C₁₁H₁₇NO₄
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MDL Number MFCD16251319
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of statins such as atorvastatin and rosuvastatin, which are widely prescribed for lowering cholesterol. Its enantiomerically pure structure allows for efficient and selective construction of the active pharmacophore in these drugs. The presence of functional groups—cyano, hydroxyl, and keto—enables further chemical transformations, making it valuable in multi-step organic syntheses. Commonly employed in asymmetric synthesis routes due to its stereochemical integrity and reactivity profile.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,820.00
inventory 1g
10-20 days ฿21,190.00

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tert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of statins such as atorvastatin and rosuvastatin, which are widely prescribed for lowering cholesterol. Its enantiomerically pure structure allows for efficient and selective construction of the active pharmacophore in these drugs. The presence of functional groups—cyano, hydroxyl, and keto—enables further chemical transformations, making it valuable in multi-step organic syntheses. Commonly employed in

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of statins such as atorvastatin and rosuvastatin, which are widely prescribed for lowering cholesterol. Its enantiomerically pure structure allows for efficient and selective construction of the active pharmacophore in these drugs. The presence of functional groups—cyano, hydroxyl, and keto—enables further chemical transformations, making it valuable in multi-step organic syntheses. Commonly employed in asymmetric synthesis routes due to its stereochemical integrity and reactivity profile.

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