4-(2-Bromoacetyl)benzoic acid

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Reagent Code: #145917
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CAS Number 20099-90-5

science Other reagents with same CAS 20099-90-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.05 g/mol
Formula C₉H₇BrO₃
thermostat Physical Properties
Melting Point 224-225°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized aromatic compounds. Its reactive bromoacetyl group allows for nucleophilic substitution reactions, making it valuable in the development of bioactive molecules and specialty chemicals. Commonly employed in the synthesis of dyes, polymers, and ligands for metal complexes. Also utilized in modifying peptides or proteins through covalent attachment due to the affinity of the bromomethyl ketone moiety for nucleophilic amino acid residues.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿310.00
inventory 1g
10-20 days ฿720.00
inventory 5g
10-20 days ฿2,860.00
inventory 25g
10-20 days ฿12,640.00

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4-(2-Bromoacetyl)benzoic acid
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized aromatic compounds. Its reactive bromoacetyl group allows for nucleophilic substitution reactions, making it valuable in the development of bioactive molecules and specialty chemicals. Commonly employed in the synthesis of dyes, polymers, and ligands for metal complexes. Also utilized in modifying peptides or proteins through covalent attachment due to the affinity of the bromomethyl ketone

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized aromatic compounds. Its reactive bromoacetyl group allows for nucleophilic substitution reactions, making it valuable in the development of bioactive molecules and specialty chemicals. Commonly employed in the synthesis of dyes, polymers, and ligands for metal complexes. Also utilized in modifying peptides or proteins through covalent attachment due to the affinity of the bromomethyl ketone moiety for nucleophilic amino acid residues.

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