2-(4-Methyl-1H-pyrazol-1-yl)acetic acid

≥95%

Reagent Code: #208835
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CAS Number 956364-44-6

science Other reagents with same CAS 956364-44-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 140.14 g/mol
Formula C₆H₈N₂O₂
badge Registry Numbers
MDL Number MFCD03419610
thermostat Physical Properties
Boiling Point 308.7±25.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

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. Its structure allows for effective binding and modulation of enzyme activity, making it valuable in medicinal chemistry. Also employed in the preparation of agrochemicals and bioactive molecules due to its stability and reactivity in coupling reactions. Commonly utilized in research settings for constructing heterocyclic compounds with potential therapeutic applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,730.00
inventory 5g
10-20 days ฿7,340.00
inventory 25g
10-20 days ฿23,740.00

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2-(4-Methyl-1H-pyrazol-1-yl)acetic acid
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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. Its structure allows for effective binding and modulation of enzyme activity, making it valuable in medicinal chemistry. Also employed in the preparation of agrochemicals and bioactive molecules due to its stability and reactivity in coupling reactions. Commonly utilized in research settings for constructing heterocyclic compounds

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. Its structure allows for effective binding and modulation of enzyme activity, making it valuable in medicinal chemistry. Also employed in the preparation of agrochemicals and bioactive molecules due to its stability and reactivity in coupling reactions. Commonly utilized in research settings for constructing heterocyclic compounds with potential therapeutic applications.

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