3-(4-Bromophenyl)propionic acid

>98.0%(GC)

Reagent Code: #143560
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CAS Number 1643-30-7

science Other reagents with same CAS 1643-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.07 g/mol
Formula BrC₆H₄CH₂CH₂CO₂H
badge Registry Numbers
MDL Number MFCD01310793
thermostat Physical Properties
Melting Point 134 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Serves as a building block in the preparation of active pharmaceutical ingredients, particularly in the development of anti-inflammatory and central nervous system agents. Also employed in the synthesis of liquid crystals and functional materials due to its aromatic and carboxylic functionality. Its bromine substituent allows for further modification via cross-coupling reactions, making it valuable in medicinal chemistry research and development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿320.00
inventory 25g
10-20 days ฿1,140.00
inventory 100g
10-20 days ฿4,540.00

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3-(4-Bromophenyl)propionic acid
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Serves as a building block in the preparation of active pharmaceutical ingredients, particularly in the development of anti-inflammatory and central nervous system agents. Also employed in the synthesis of liquid crystals and functional materials due to its aromatic and carboxylic functionality. Its bromine substituent allows for further modification via cross-coupling reactions, making it valuable in medicinal chemistry

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Serves as a building block in the preparation of active pharmaceutical ingredients, particularly in the development of anti-inflammatory and central nervous system agents. Also employed in the synthesis of liquid crystals and functional materials due to its aromatic and carboxylic functionality. Its bromine substituent allows for further modification via cross-coupling reactions, making it valuable in medicinal chemistry research and development.

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