2-Amino-5-chlorobenzoic acid

98%

Reagent Code: #135089
label
Alias 5-Chloro-o-aminobenzoic acid
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CAS Number 635-21-2

science Other reagents with same CAS 635-21-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.58 g/mol
Formula H₂NC₆H₃(Cl)CO₂H
badge Registry Numbers
EC Number 211-230-8
MDL Number MFCD00007838
thermostat Physical Properties
Melting Point 204-206 °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 non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. It serves as a building block in the development of dyes, agrochemicals, and specialty polymers due to its functional amino and carboxylic acid groups. Its chlorinated aromatic structure makes it valuable in cross-coupling reactions for creating complex organic molecules. Also employed in research for designing new compounds with potential antimicrobial or antitumor activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿450.00
inventory 100g
10-20 days ฿740.00
inventory 500g
10-20 days ฿3,470.00

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2-Amino-5-chlorobenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. It serves as a building block in the development of dyes, agrochemicals, and specialty polymers due to its functional amino and carboxylic acid groups. Its chlorinated aromatic structure makes it valuable in cross-coupling reactions for creating complex organic molecules. Also employed in research for designing new compounds with pote

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. It serves as a building block in the development of dyes, agrochemicals, and specialty polymers due to its functional amino and carboxylic acid groups. Its chlorinated aromatic structure makes it valuable in cross-coupling reactions for creating complex organic molecules. Also employed in research for designing new compounds with potential antimicrobial or antitumor activity.

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