Ethyl 4-bromophenylacetate

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Reagent Code: #182050
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Alias Ethyl p-bromophenylacetate
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CAS Number 14062-25-0

science Other reagents with same CAS 14062-25-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.10 g/mol
Formula C₁₀H₁₁BrO₂
badge Registry Numbers
MDL Number MFCD00016333
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for the preparation of active ingredients in certain drug compounds, especially those requiring substituted phenylacetic acid derivatives. Its bromine functionality allows for further transformations via cross-coupling reactions, enabling the construction of more complex molecules. Also employed in the synthesis of fragrances and specialty esters due to its stable ester group and reactive aromatic site.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿710.00
inventory 100g
10-20 days ฿2,320.00
inventory 500g
10-20 days ฿9,810.00

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Ethyl 4-bromophenylacetate
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for the preparation of active ingredients in certain drug compounds, especially those requiring substituted phenylacetic acid derivatives. Its bromine functionality allows for further transformations via cross-coupling reactions, enabling the construction of more complex molecules. Also employed in the synthesis of fragrances and specialty esters due to its stab

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for the preparation of active ingredients in certain drug compounds, especially those requiring substituted phenylacetic acid derivatives. Its bromine functionality allows for further transformations via cross-coupling reactions, enabling the construction of more complex molecules. Also employed in the synthesis of fragrances and specialty esters due to its stable ester group and reactive aromatic site.

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