4-Bromo-2-(trifluoromethyl)benzoic acid

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Reagent Code: #143437
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CAS Number 320-31-0

science Other reagents with same CAS 320-31-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.02 g/mol
Formula C₈H₄BrF₃O₂
badge Registry Numbers
MDL Number MFCD07787468
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for selective functionalization in drug design, making it valuable in creating active pharmaceutical ingredients (APIs) with enhanced metabolic stability. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex aromatic systems. Also utilized in agrochemicals for the production of herbicides and fungicides due to the electron-withdrawing nature of the trifluoromethyl group, which improves bioavailability and environmental persistence. Suitable for research in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿148.50
inventory 1g
10-20 days ฿154.00
inventory 5g
10-20 days ฿450.00
inventory 25g
10-20 days ฿2,010.00
inventory 500g
10-20 days ฿36,880.00
inventory 100g
10-20 days ฿7,530.00

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4-Bromo-2-(trifluoromethyl)benzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for selective functionalization in drug design, making it valuable in creating active pharmaceutical ingredients (APIs) with enhanced metabolic stability. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex aromatic systems. Also utilized in agrochemicals for the production of herbicides and fungicides d

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for selective functionalization in drug design, making it valuable in creating active pharmaceutical ingredients (APIs) with enhanced metabolic stability. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex aromatic systems. Also utilized in agrochemicals for the production of herbicides and fungicides due to the electron-withdrawing nature of the trifluoromethyl group, which improves bioavailability and environmental persistence. Suitable for research in medicinal chemistry for structure-activity relationship (SAR) studies.

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