Ethyl 2-(2-chlorophenyl)-2-oxoacetate

≥95%

Reagent Code: #183580
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CAS Number 62123-75-5

science Other reagents with same CAS 62123-75-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.63 g/mol
Formula C₁₀H₉ClO₃
badge Registry Numbers
MDL Number MFCD09801392
thermostat Physical Properties
Boiling Point 304.921°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.255g/cm3
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the preparation of anticoagulant and anti-inflammatory agents. It serves as a building block in organic reactions where the ester and keto functionalities allow for further chemical modifications. Commonly employed in the formation of heterocyclic compounds through cyclization reactions. Also utilized in the development of agrochemicals and dyes due to its reactive α-keto ester structure. Its chlorophenyl group enhances reactivity in cross-coupling reactions, making it valuable in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,510.00
inventory 250mg
10-20 days ฿5,870.00
inventory 1g
10-20 days ฿15,330.00

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Ethyl 2-(2-chlorophenyl)-2-oxoacetate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the preparation of anticoagulant and anti-inflammatory agents. It serves as a building block in organic reactions where the ester and keto functionalities allow for further chemical modifications. Commonly employed in the formation of heterocyclic compounds through cyclization reactions. Also utilized in the development of agrochemicals and dyes due to its reactive α-keto ester structure. Its chlorophenyl group enhances reactivi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the preparation of anticoagulant and anti-inflammatory agents. It serves as a building block in organic reactions where the ester and keto functionalities allow for further chemical modifications. Commonly employed in the formation of heterocyclic compounds through cyclization reactions. Also utilized in the development of agrochemicals and dyes due to its reactive α-keto ester structure. Its chlorophenyl group enhances reactivity in cross-coupling reactions, making it valuable in medicinal chemistry research.

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