3-Cyano-4-hydroxybenzoic acid

≥95%

Reagent Code: #161864
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CAS Number 70829-28-6

science Other reagents with same CAS 70829-28-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.13 g/mol
Formula C₈H₅NO₃
badge Registry Numbers
MDL Number MFCD09998350
thermostat Physical Properties
Boiling Point 392.447°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of nabumetone. It serves as a building block in pharmaceuticals due to its functional groups, which allow for further chemical modifications. The cyano and carboxylic acid groups enable coupling reactions and ring formations important in drug development. Also employed in the preparation of dyes and functional organic materials where aromatic carboxylic acids with electron-withdrawing substituents are required.

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Test Parameter Specification
Appearance Solid
Purity (%) 95-100%
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,460.00
inventory 5g
10-20 days ฿13,720.00
inventory 10g
10-20 days ฿24,930.00
inventory 1g
10-20 days ฿3,200.00

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3-Cyano-4-hydroxybenzoic acid
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Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of nabumetone. It serves as a building block in pharmaceuticals due to its functional groups, which allow for further chemical modifications. The cyano and carboxylic acid groups enable coupling reactions and ring formations important in drug development. Also employed in the preparation of dyes and functional organic materials where aromatic carboxylic acids with electron-withdra

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of nabumetone. It serves as a building block in pharmaceuticals due to its functional groups, which allow for further chemical modifications. The cyano and carboxylic acid groups enable coupling reactions and ring formations important in drug development. Also employed in the preparation of dyes and functional organic materials where aromatic carboxylic acids with electron-withdrawing substituents are required.

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