4-Amino-2-chlorobenzoic acid

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Reagent Code: #134978
label
Alias 2-Chloro-4-Aminobenzoic Acid
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CAS Number 2457-76-3

science Other reagents with same CAS 2457-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.58 g/mol
Formula C₇H₆ClNO₂
badge Registry Numbers
EC Number 219-540-5
MDL Number MFCD00007772
thermostat Physical Properties
Melting Point 211 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nonsteroidal anti-inflammatory drugs (NSAIDs) like diclofenac. It serves as a building block for constructing more complex molecules due to the presence of both amino and carboxylic acid functional groups, which allow for diverse chemical modifications. Also employed in the development of agrochemicals and dyes, where its chloro and amino substituents facilitate specific reaction pathways. Its structure supports conjugation in organic synthesis, making it valuable in research and industrial applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿550.00
inventory 25g
10-20 days ฿2,490.00
inventory 100g
10-20 days ฿9,360.00
inventory 500g
10-20 days ฿45,390.00

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4-Amino-2-chlorobenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nonsteroidal anti-inflammatory drugs (NSAIDs) like diclofenac. It serves as a building block for constructing more complex molecules due to the presence of both amino and carboxylic acid functional groups, which allow for diverse chemical modifications. Also employed in the development of agrochemicals and dyes, where its chloro and amino substituents facilitate specific reaction pathways. Its structure support

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nonsteroidal anti-inflammatory drugs (NSAIDs) like diclofenac. It serves as a building block for constructing more complex molecules due to the presence of both amino and carboxylic acid functional groups, which allow for diverse chemical modifications. Also employed in the development of agrochemicals and dyes, where its chloro and amino substituents facilitate specific reaction pathways. Its structure supports conjugation in organic synthesis, making it valuable in research and industrial applications.

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