3-(Cyanomethyl)benzoic acid

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Reagent Code: #160460
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CAS Number 5689-33-8

science Other reagents with same CAS 5689-33-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.16 g/mol
Formula C₉H₇NO₂
thermostat Physical Properties
Melting Point 175-176°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting the central nervous system. It serves as a building block for gamma-aminobutyric acid (GABA) analogs due to the presence of both carboxylic acid and cyanomethyl functional groups. The compound is also employed in the preparation of agrochemicals and specialty polymers, where its reactive groups allow for further chemical modifications. Its structural features make it valuable in medicinal chemistry for creating bioactive molecules with enhanced stability and binding properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,020.00
inventory 1g
10-20 days ฿3,680.00

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3-(Cyanomethyl)benzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting the central nervous system. It serves as a building block for gamma-aminobutyric acid (GABA) analogs due to the presence of both carboxylic acid and cyanomethyl functional groups. The compound is also employed in the preparation of agrochemicals and specialty polymers, where its reactive groups allow for further chemical modifications. Its structural features make it valuable in medicinal chemi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting the central nervous system. It serves as a building block for gamma-aminobutyric acid (GABA) analogs due to the presence of both carboxylic acid and cyanomethyl functional groups. The compound is also employed in the preparation of agrochemicals and specialty polymers, where its reactive groups allow for further chemical modifications. Its structural features make it valuable in medicinal chemistry for creating bioactive molecules with enhanced stability and binding properties.

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