(R)-4-Chloro-3-hydroxybutyric Acid Ethyl Ester

90%(GC)

Reagent Code: #230010
label
Alias (R) 4-chloro-3-hydroxybutyrate ethyl ester; (R) 4-chloro-3-hydroxyn-butyrate ethyl ester
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CAS Number 90866-33-4

science Other reagents with same CAS 90866-33-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.6 g/mol
Formula C₆H₁₁ClO₃
badge Registry Numbers
MDL Number MFCD00211242
thermostat Physical Properties
Melting Point 93-95 °C
Boiling Point 93-95 °C (5 mmHg)
inventory_2 Storage & Handling
Density 1.19
Storage Room temperature

description Product Description

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the production of statins such as atorvastatin and rosuvastatin, which are widely prescribed for lowering cholesterol. Its stereochemistry allows for high selectivity in asymmetric synthesis, improving the efficiency and purity of the final drug product. Commonly employed in multi-step organic transformations where a protected hydroxy acid functionality with a chlorine substituent is required. Also utilized in the preparation of biologically active molecules and intermediates in fine chemical manufacturing.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿170.50
inventory 25g
10-20 days ฿960.00
(R)-4-Chloro-3-hydroxybutyric Acid Ethyl Ester
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Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the production of statins such as atorvastatin and rosuvastatin, which are widely prescribed for lowering cholesterol. Its stereochemistry allows for high selectivity in asymmetric synthesis, improving the efficiency and purity of the final drug product. Commonly employed in multi-step organic transformations where a protected hydroxy acid functionality with a chlorine substituent is required. Also utilized in the pr

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the production of statins such as atorvastatin and rosuvastatin, which are widely prescribed for lowering cholesterol. Its stereochemistry allows for high selectivity in asymmetric synthesis, improving the efficiency and purity of the final drug product. Commonly employed in multi-step organic transformations where a protected hydroxy acid functionality with a chlorine substituent is required. Also utilized in the preparation of biologically active molecules and intermediates in fine chemical manufacturing.

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