4-Amino-5-bromo-2-fluorobenzoic acid

95%

Reagent Code: #138464
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CAS Number 1807757-07-8

science Other reagents with same CAS 1807757-07-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.0225 g/mol
Formula C₇H₅BrFNO₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated and brominated aromatic compounds. Its structure supports the creation of active ingredients in drugs targeting inflammatory conditions and central nervous system disorders. The presence of both amino and carboxylic acid functional groups allows for peptide coupling and derivatization, making it valuable in medicinal chemistry for building complex molecules. Also employed in the preparation of agrochemicals and specialty organic materials requiring halogenated aromatic backbones.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,590.00
inventory 250mg
10-20 days ฿3,870.00
inventory 1g
10-20 days ฿9,650.00
inventory 5g
10-20 days ฿37,110.00
inventory 10g
10-20 days ฿64,530.00

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4-Amino-5-bromo-2-fluorobenzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated and brominated aromatic compounds. Its structure supports the creation of active ingredients in drugs targeting inflammatory conditions and central nervous system disorders. The presence of both amino and carboxylic acid functional groups allows for peptide coupling and derivatization, making it valuable in medicinal chemistry for building complex molecules. Also employed in the preparation of a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated and brominated aromatic compounds. Its structure supports the creation of active ingredients in drugs targeting inflammatory conditions and central nervous system disorders. The presence of both amino and carboxylic acid functional groups allows for peptide coupling and derivatization, making it valuable in medicinal chemistry for building complex molecules. Also employed in the preparation of agrochemicals and specialty organic materials requiring halogenated aromatic backbones.

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