2-Amino-4-methoxybenzoic acid

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Reagent Code: #134971
label
Alias 2-amino orthanis acid; 4-methoxy anthranilic acid; m-anisone-6-carboxylic acid
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CAS Number 4294-95-5

science Other reagents with same CAS 4294-95-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.16 g/mol
Formula C₈H₉NO₃
badge Registry Numbers
MDL Number MFCD00667729
thermostat Physical Properties
Melting Point 174-177°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly for azo dyes, due to its aromatic amine group that facilitates diazotization and coupling reactions. It also serves in the preparation of pharmaceuticals, where the amino and methoxy functionalities contribute to building active compounds, especially in anti-inflammatory or analgesic agents. Additionally, it finds use in agrochemicals for developing herbicides and plant growth regulators. Its structure, featuring a carboxylic acid group, allows for easy modification, making it valuable in organic synthesis and research for developing new functional molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿1,090.00
inventory 25g
10-20 days ฿5,350.00

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2-Amino-4-methoxybenzoic acid
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Used as an intermediate in the synthesis of dyes and pigments, particularly for azo dyes, due to its aromatic amine group that facilitates diazotization and coupling reactions. It also serves in the preparation of pharmaceuticals, where the amino and methoxy functionalities contribute to building active compounds, especially in anti-inflammatory or analgesic agents. Additionally, it finds use in agrochemicals for developing herbicides and plant growth regulators. Its structure, featuring a carboxylic aci

Used as an intermediate in the synthesis of dyes and pigments, particularly for azo dyes, due to its aromatic amine group that facilitates diazotization and coupling reactions. It also serves in the preparation of pharmaceuticals, where the amino and methoxy functionalities contribute to building active compounds, especially in anti-inflammatory or analgesic agents. Additionally, it finds use in agrochemicals for developing herbicides and plant growth regulators. Its structure, featuring a carboxylic acid group, allows for easy modification, making it valuable in organic synthesis and research for developing new functional molecules.

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