Ethyl 2-oxo-4-phenylbutyrate

92%

Reagent Code: #181565
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Alias 2-oxo-4-phenylbutyrate
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CAS Number 64920-29-2

science Other reagents with same CAS 64920-29-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.24 g/mol
Formula C₁₂H₁₄O₃
badge Registry Numbers
EC Number 265-276-9
MDL Number MFCD00037533
thermostat Physical Properties
Boiling Point 132 °C2 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.091 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of angiotensin-converting enzyme (ACE) inhibitors, such as Captopril, a drug for treating hypertension and heart failure. Its ketoester structure allows for selective chemical modifications, making it valuable in pharmaceutical manufacturing. Also employed in organic synthesis to build chiral molecules through asymmetric reduction or enolate chemistry. Commonly used in research settings for developing biologically active compounds and heterocyclic derivatives.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,150.00
inventory 25g
10-20 days ฿5,630.00
inventory 100g
10-20 days ฿14,340.00
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Ethyl 2-oxo-4-phenylbutyrate
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Used as a key intermediate in the synthesis of angiotensin-converting enzyme (ACE) inhibitors, such as Captopril, a drug for treating hypertension and heart failure. Its ketoester structure allows for selective chemical modifications, making it valuable in pharmaceutical manufacturing. Also employed in organic synthesis to build chiral molecules through asymmetric reduction or enolate chemistry. Commonly used in research settings for developing biologically active compounds and heterocyclic derivatives.<

Used as a key intermediate in the synthesis of angiotensin-converting enzyme (ACE) inhibitors, such as Captopril, a drug for treating hypertension and heart failure. Its ketoester structure allows for selective chemical modifications, making it valuable in pharmaceutical manufacturing. Also employed in organic synthesis to build chiral molecules through asymmetric reduction or enolate chemistry. Commonly used in research settings for developing biologically active compounds and heterocyclic derivatives.

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