2-Amino-3-methoxybenzoic acid

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Reagent Code: #135237
label
Alias 2-amino-methanisic acid; 3-methoxy anthanisin-6-carboxylic acid
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CAS Number 3177-80-8

science Other reagents with same CAS 3177-80-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.16 g/mol
Formula C₈H₉NO₃
badge Registry Numbers
MDL Number MFCD00075178
inventory_2 Storage & Handling
Storage Room temperature, sealed

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 the preparation of heterocyclic compounds, including benzoxazoles and quinazolines, which are important in medicinal chemistry. Also employed in the production of dyes and pigments due to its aromatic amine functionality. Its methoxy and amino groups allow for selective modifications in organic synthesis, making it valuable in research laboratories for designing complex molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿340.00
inventory 5g
10-20 days ฿1,120.00
inventory 25g
10-20 days ฿5,230.00
inventory 100g
10-20 days ฿16,860.00

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2-Amino-3-methoxybenzoic 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 the preparation of heterocyclic compounds, including benzoxazoles and quinazolines, which are important in medicinal chemistry. Also employed in the production of dyes and pigments due to its aromatic amine functionality. Its methoxy and amino groups allow for selective modifications in organic synthesis, making it valuable in research labora
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 the preparation of heterocyclic compounds, including benzoxazoles and quinazolines, which are important in medicinal chemistry. Also employed in the production of dyes and pigments due to its aromatic amine functionality. Its methoxy and amino groups allow for selective modifications in organic synthesis, making it valuable in research laboratories for designing complex molecules.
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