Ethyl 3-bromobenzoate

98%

Reagent Code: #181555
label
Alias Ethyl bromobenzoate
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CAS Number 24398-88-7

science Other reagents with same CAS 24398-88-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.07 g/mol
Formula C₉H₉BrO₂
badge Registry Numbers
EC Number 246-223-9
MDL Number MFCD00013529
thermostat Physical Properties
Boiling Point 261.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.431 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. It serves as a building block for constructing more complex molecules due to the presence of both ester and bromo functional groups. The bromine atom allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The ester group can be hydrolyzed to yield carboxylic acids or reduced to alcohols, adding versatility in synthetic pathways. Commonly employed in the development of active pharmaceutical ingredients and functionalized aromatic compounds.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,360.00
inventory 100g
10-20 days ฿5,170.00
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Ethyl 3-bromobenzoate
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Used as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. It serves as a building block for constructing more complex molecules due to the presence of both ester and bromo functional groups. The bromine atom allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The ester group can be hydrolyzed to yield carboxylic acids or reduced to alcohols, adding versatility in synthetic pathways. Commonly employed

Used as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. It serves as a building block for constructing more complex molecules due to the presence of both ester and bromo functional groups. The bromine atom allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The ester group can be hydrolyzed to yield carboxylic acids or reduced to alcohols, adding versatility in synthetic pathways. Commonly employed in the development of active pharmaceutical ingredients and functionalized aromatic compounds.

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