2-Amino-3-bromobenzoic acid

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Reagent Code: #134970
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CAS Number 20776-51-6

science Other reagents with same CAS 20776-51-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.03 g/mol
Formula C₇H₆BrNO₂
badge Registry Numbers
MDL Number MFCD03618453
thermostat Physical Properties
Melting Point 173 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and dyes. It participates in the preparation of heterocyclic compounds, particularly benzoxazoles and quinazolines, which are important in medicinal chemistry. Commonly employed in the development of analgesic and anti-inflammatory agents. Also utilized in research settings for the modification of organic molecules requiring amino and carboxylic functional groups in close proximity with a bromine handle for further derivatization.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿162.00
inventory 5g
10-20 days ฿510.00
inventory 25g
10-20 days ฿2,080.00
inventory 100g
10-20 days ฿8,200.00

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2-Amino-3-bromobenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and dyes. It participates in the preparation of heterocyclic compounds, particularly benzoxazoles and quinazolines, which are important in medicinal chemistry. Commonly employed in the development of analgesic and anti-inflammatory agents. Also utilized in research settings for the modification of organic molecules requiring amino and carboxylic functional groups in close proximity with a bromine handle for further derivatization.

Used as an intermediate in the synthesis of pharmaceuticals and dyes. It participates in the preparation of heterocyclic compounds, particularly benzoxazoles and quinazolines, which are important in medicinal chemistry. Commonly employed in the development of analgesic and anti-inflammatory agents. Also utilized in research settings for the modification of organic molecules requiring amino and carboxylic functional groups in close proximity with a bromine handle for further derivatization.

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