Ethyl 4-(2-oxopropyl)benzoate

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Reagent Code: #183572
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CAS Number 73013-51-1

science Other reagents with same CAS 73013-51-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.24 g/mol
Formula C₁₂H₁₄O₃
badge Registry Numbers
MDL Number MFCD02261282
thermostat Physical Properties
Boiling Point 310.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.083g/cm3
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure allows for functional group transformations, such as reduction of the ketone or ester moieties, enabling the construction of more complex molecules. Commonly employed in the development of active pharmaceutical ingredients where a substituted aromatic ester with a side chain ketone is required. Also utilized in research settings for the synthesis of analogs in medicinal chemistry programs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,000.00

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Ethyl 4-(2-oxopropyl)benzoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure allows for functional group transformations, such as reduction of the ketone or ester moieties, enabling the construction of more complex molecules. Commonly employed in the development of active pharmaceutical ingredients where a substituted aromatic ester with a side chain ketone is required. Also utilized in research settings for the synthesis of analogs in medicinal chemi

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure allows for functional group transformations, such as reduction of the ketone or ester moieties, enabling the construction of more complex molecules. Commonly employed in the development of active pharmaceutical ingredients where a substituted aromatic ester with a side chain ketone is required. Also utilized in research settings for the synthesis of analogs in medicinal chemistry programs.

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