1-Phenyl-1H-pyrazol-3-amine

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Reagent Code: #226269
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CAS Number 1128-56-9

science Other reagents with same CAS 1128-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.19 g/mol
Formula C₉H₉N₃
badge Registry Numbers
MDL Number MFCD00100520
thermostat Physical Properties
Boiling Point 323.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. It serves as a building block in agrochemicals for creating herbicides and fungicides due to its stable heterocyclic structure. Also employed in the preparation of dyes and fluorescent probes for biochemical labeling. Its amine functionality allows easy modification for use in combinatorial chemistry and drug discovery research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,560.00
inventory 1g
10-20 days ฿3,990.00
inventory 5g
10-20 days ฿17,280.00
inventory 10g
10-20 days ฿30,300.00
inventory 25g
10-20 days ฿63,540.00

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1-Phenyl-1H-pyrazol-3-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. It serves as a building block in agrochemicals for creating herbicides and fungicides due to its stable heterocyclic structure. Also employed in the preparation of dyes and fluorescent probes for biochemical labeling. Its amine functionality allows easy modification for use in combinatorial chemistry and drug discovery research.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. It serves as a building block in agrochemicals for creating herbicides and fungicides due to its stable heterocyclic structure. Also employed in the preparation of dyes and fluorescent probes for biochemical labeling. Its amine functionality allows easy modification for use in combinatorial chemistry and drug discovery research.

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