Ethyl 2-bromobenzoate

99%

Reagent Code: #182071
label
Alias Ethyl 2-bromobenzoate; Ethyl ortho-bromobenzoate
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CAS Number 6091-64-1

science Other reagents with same CAS 6091-64-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.07 g/mol
Formula C₉H₉BrO₂
badge Registry Numbers
MDL Number MFCD00015443
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the formation of heterocyclic compounds and is employed in the synthesis of local anesthetics such as benzocaine and procaine. Its bromine functionality allows for further transformations via cross-coupling reactions, making it valuable in medicinal chemistry and the development of active pharmaceutical ingredients. Additionally, it finds use in research settings for studying reaction mechanisms involving ester and aryl halide functional groups.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿174.00
25g
10-20 days ฿500.00
100g
10-20 days ฿1,880.00
500g
10-20 days ฿9,080.00
Ethyl 2-bromobenzoate
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Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the formation of heterocyclic compounds and is employed in the synthesis of local anesthetics such as benzocaine and procaine. Its bromine functionality allows for further transformations via cross-coupling reactions, making it valuable in medicinal chemistry and the development of active pharmaceutical ingredients. Additionally, it finds use in r

Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the formation of heterocyclic compounds and is employed in the synthesis of local anesthetics such as benzocaine and procaine. Its bromine functionality allows for further transformations via cross-coupling reactions, making it valuable in medicinal chemistry and the development of active pharmaceutical ingredients. Additionally, it finds use in research settings for studying reaction mechanisms involving ester and aryl halide functional groups.

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