2-Bromo-4-fluorobenzoic acid

98%

Reagent Code: #143410
label
Alias 2-Bromo-4-Fluorobenzoic acid
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CAS Number 1006-41-3

science Other reagents with same CAS 1006-41-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.01 g/mol
Formula C₇H₄BrFO₂
badge Registry Numbers
MDL Number MFCD00055370
thermostat Physical Properties
Melting Point 172-176 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and anti-inflammatory agents. Its structure allows for selective functionalization in organic reactions, making it valuable in building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions to form biaryl compounds. Also utilized in agrochemical synthesis for creating herbicides and fungicides due to its halogenated aromatic framework. Serves as a building block in medicinal chemistry for structure-activity relationship (SAR) studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿168.00
5g
10-20 days ฿340.00
25g
10-20 days ฿1,140.00
100g
10-20 days ฿4,010.00
2-Bromo-4-fluorobenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and anti-inflammatory agents. Its structure allows for selective functionalization in organic reactions, making it valuable in building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions to form biaryl compounds. Also utilized in agrochemical synthesis for creati

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and anti-inflammatory agents. Its structure allows for selective functionalization in organic reactions, making it valuable in building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions to form biaryl compounds. Also utilized in agrochemical synthesis for creating herbicides and fungicides due to its halogenated aromatic framework. Serves as a building block in medicinal chemistry for structure-activity relationship (SAR) studies.

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