3-Amino-5-chlorobenzoic acid

98%

Reagent Code: #135092
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CAS Number 21961-30-8

science Other reagents with same CAS 21961-30-8

blur_circular Chemical Specifications

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Weight 171.58 g/mol
Formula C₇H₆ClNO₂
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 organic synthesis due to the presence of both amino and carboxylic acid functional groups, allowing for coupling reactions and the formation of amides, esters, and heterocyclic compounds. Also employed in the development of agrochemicals and dyes where substituted aromatic amines are required. Its chloro substituent enables further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,860.00
inventory 5g
10-20 days ฿8,040.00
inventory 25g
10-20 days ฿25,970.00

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3-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 organic synthesis due to the presence of both amino and carboxylic acid functional groups, allowing for coupling reactions and the formation of amides, esters, and heterocyclic compounds. Also employed in the development of agrochemicals and dyes where substituted aromatic amines are required. Its chlo

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 organic synthesis due to the presence of both amino and carboxylic acid functional groups, allowing for coupling reactions and the formation of amides, esters, and heterocyclic compounds. Also employed in the development of agrochemicals and dyes where substituted aromatic amines are required. Its chloro substituent enables further functionalization through cross-coupling reactions, expanding its utility in medicinal chemistry research.

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