Ethyl 3-(2-chloroacetamido)benzoate

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Reagent Code: #184624
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CAS Number 58915-19-8

science Other reagents with same CAS 58915-19-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.67 g/mol
Formula C₁₁H₁₂ClNO₃
badge Registry Numbers
MDL Number MFCD00711338
thermostat Physical Properties
Boiling Point 417.8±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.283±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It plays a role in the development of bioactive molecules due to the presence of both ester and chloroacetamido functional groups, which can undergo further transformations. Commonly employed in the synthesis of heterocyclic compounds and drug candidates targeting inflammation and central nervous system disorders. Its reactivity allows for selective modifications, making it valuable in medicinal chemistry research and development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,020.00
inventory 5g
10-20 days ฿10,540.00
inventory 250mg
10-20 days ฿2,050.00

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Ethyl 3-(2-chloroacetamido)benzoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It plays a role in the development of bioactive molecules due to the presence of both ester and chloroacetamido functional groups, which can undergo further transformations. Commonly employed in the synthesis of heterocyclic compounds and drug candidates targeting inflammation and central nervous system disorders. Its reactivity allows for selective modifications, making it valuable in medicinal che

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It plays a role in the development of bioactive molecules due to the presence of both ester and chloroacetamido functional groups, which can undergo further transformations. Commonly employed in the synthesis of heterocyclic compounds and drug candidates targeting inflammation and central nervous system disorders. Its reactivity allows for selective modifications, making it valuable in medicinal chemistry research and development.

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