Ethyl (R)-(-)-2-hydroxy-4-phenylbutyrate

98 %

Reagent Code: #181785
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CAS Number 90315-82-5

science Other reagents with same CAS 90315-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.25 g/mol
Formula C₁₂H₁₆O₃
badge Registry Numbers
MDL Number MFCD00077794
thermostat Physical Properties
Melting Point NA
Boiling Point 212 °C(lit.)
inventory_2 Storage & Handling
Density 1.075 g/mL at 20 °C(lit.)
Storage Room temperature, dry, sealed

description Product Description

Used as a chiral building block in the synthesis of angiotensin-converting enzyme (ACE) inhibitors, such as benazepril and other pharmaceuticals targeting hypertension. Its enantiomeric purity is critical for effective drug performance, making it valuable in asymmetric synthesis. Commonly employed in esterification and reduction reactions to form key intermediates in active pharmaceutical ingredients (APIs). Also utilized in the preparation of beta-amino acids and other bioactive molecules requiring stereochemical control.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿126.00
inventory 5g
10-20 days ฿330.00
inventory 25g
10-20 days ฿1,400.00
inventory 100g
10-20 days ฿3,300.00
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Ethyl (R)-(-)-2-hydroxy-4-phenylbutyrate
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Used as a chiral building block in the synthesis of angiotensin-converting enzyme (ACE) inhibitors, such as benazepril and other pharmaceuticals targeting hypertension. Its enantiomeric purity is critical for effective drug performance, making it valuable in asymmetric synthesis. Commonly employed in esterification and reduction reactions to form key intermediates in active pharmaceutical ingredients (APIs). Also utilized in the preparation of beta-amino acids and other bioactive molecules requiring ster

Used as a chiral building block in the synthesis of angiotensin-converting enzyme (ACE) inhibitors, such as benazepril and other pharmaceuticals targeting hypertension. Its enantiomeric purity is critical for effective drug performance, making it valuable in asymmetric synthesis. Commonly employed in esterification and reduction reactions to form key intermediates in active pharmaceutical ingredients (APIs). Also utilized in the preparation of beta-amino acids and other bioactive molecules requiring stereochemical control.

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