2-Amino-3,4-dimethoxybenzoic acid

95%

Reagent Code: #137033
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CAS Number 5701-87-1

science Other reagents with same CAS 5701-87-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.19 g/mol
Formula C₉H₁₁NO₄
badge Registry Numbers
MDL Number MFCD00038792
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of analgesic and anti-inflammatory drugs. It serves as a building block in organic synthesis due to the presence of both amino and carboxylic acid functional groups, enabling peptide coupling and ring modification reactions. Also employed in the preparation of dyes and functionalized heterocyclic compounds for research applications. Its methoxy groups enhance electron density, making it useful in reactions requiring nucleophilic aromatic substitution.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,320.00
inventory 250mg
10-20 days ฿3,250.00
inventory 1g
10-20 days ฿12,130.00
inventory 5g
10-20 days ฿47,770.00

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2-Amino-3,4-dimethoxybenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of analgesic and anti-inflammatory drugs. It serves as a building block in organic synthesis due to the presence of both amino and carboxylic acid functional groups, enabling peptide coupling and ring modification reactions. Also employed in the preparation of dyes and functionalized heterocyclic compounds for research applications. Its methoxy groups enhance electron density, making it useful in reactions requir

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of analgesic and anti-inflammatory drugs. It serves as a building block in organic synthesis due to the presence of both amino and carboxylic acid functional groups, enabling peptide coupling and ring modification reactions. Also employed in the preparation of dyes and functionalized heterocyclic compounds for research applications. Its methoxy groups enhance electron density, making it useful in reactions requiring nucleophilic aromatic substitution.

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