3-(Aminomethyl)benzoic acid

≥95%

Reagent Code: #137543
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CAS Number 2393-20-6

science Other reagents with same CAS 2393-20-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.16 g/mol
Formula C₈H₉NO₂
badge Registry Numbers
MDL Number MFCD03410969
inventory_2 Storage & Handling
Storage 2-8℃, dry, sealed

description Product Description

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of drugs targeting the central nervous system. It serves as a building block for gamma-aminobutyric acid (GABA) analogs, which are important in treating neurological disorders such as epilepsy and neuropathic pain. Also utilized in the development of novel receptor ligands due to its structural compatibility with bioactive molecules. Its bifunctional nature—bearing both amine and carboxylic acid groups—makes it valuable in medicinal chemistry for creating amide bonds and other conjugates in drug design.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,600.00
inventory 5g
10-20 days ฿25,740.00

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3-(Aminomethyl)benzoic acid
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Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of drugs targeting the central nervous system. It serves as a building block for gamma-aminobutyric acid (GABA) analogs, which are important in treating neurological disorders such as epilepsy and neuropathic pain. Also utilized in the development of novel receptor ligands due to its structural compatibility with bioactive molecules. Its bifunctional nature—bearing both amine and carboxylic acid groups—makes it va

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of drugs targeting the central nervous system. It serves as a building block for gamma-aminobutyric acid (GABA) analogs, which are important in treating neurological disorders such as epilepsy and neuropathic pain. Also utilized in the development of novel receptor ligands due to its structural compatibility with bioactive molecules. Its bifunctional nature—bearing both amine and carboxylic acid groups—makes it valuable in medicinal chemistry for creating amide bonds and other conjugates in drug design.

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