2-Amino-6-chlorobenzoic acid

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Reagent Code: #135221
label
Alias 2-amino-6-chlorobenzoic acid
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CAS Number 2148-56-3

science Other reagents with same CAS 2148-56-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.58 g/mol
Formula C₇H₆ClNO₂
badge Registry Numbers
EC Number 218-416-8
MDL Number MFCD00051530
thermostat Physical Properties
Melting Point 158-160 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nonsteroidal 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 versatile chemical modifications. Commonly employed in the development of dyes, agrochemicals, and specialty polymers where chloro-substituted aromatic amines are required. Its structure supports conjugation in heterocyclic compound formation, making it valuable in medicinal chemistry for drug design and optimization.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿150.00
inventory 25g
10-20 days ฿350.00
inventory 100g
10-20 days ฿1,080.00
inventory 500g
10-20 days ฿5,150.00

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2-Amino-6-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) 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 versatile chemical modifications. Commonly employed in the development of dyes, agrochemicals, and specialty polymers where chloro-substituted aromatic amines are required. Its structure supports conj

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nonsteroidal 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 versatile chemical modifications. Commonly employed in the development of dyes, agrochemicals, and specialty polymers where chloro-substituted aromatic amines are required. Its structure supports conjugation in heterocyclic compound formation, making it valuable in medicinal chemistry for drug design and optimization.

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