Ethyl 3-(4-bromophenyl)propanoate

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Reagent Code: #182036
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CAS Number 40640-98-0

science Other reagents with same CAS 40640-98-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.13 g/mol
Formula C₁₁H₁₃BrO₂
badge Registry Numbers
MDL Number MFCD07772961
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure allows for further functionalization, making it valuable in the development of active pharmaceutical ingredients (APIs) where brominated aromatic systems are needed. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex molecules. Also utilized in the synthesis of fragrances and specialty esters due to its ester functionality and aromatic backbone.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿770.00
inventory 25g
10-20 days ฿3,590.00
inventory 100g
10-20 days ฿12,560.00
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Ethyl 3-(4-bromophenyl)propanoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure allows for further functionalization, making it valuable in the development of active pharmaceutical ingredients (APIs) where brominated aromatic systems are needed. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex molecules. Also utilized in the synthesis of fragrances and specialty esters due to its ester functionality and ar

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure allows for further functionalization, making it valuable in the development of active pharmaceutical ingredients (APIs) where brominated aromatic systems are needed. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex molecules. Also utilized in the synthesis of fragrances and specialty esters due to its ester functionality and aromatic backbone.

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