3-Methyl-1H-Pyrazole-5-Carboxylic Acid Ethyl Ester

≥96%

Reagent Code: #207702
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CAS Number 886495-75-6

science Other reagents with same CAS 886495-75-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.17 g/mol
Formula C₇H₁₀N₂O₂
thermostat Physical Properties
Melting Point 80-84ºC
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory, analgesic, and antipyretic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of pyrazole-containing compounds that are important in medicinal research. Its ester functionality allows for further chemical modifications, making it valuable in optimizing drug candidates during the discovery phase. Also employed in agrochemical research for designing new crop protection agents due to its ability to enhance molecular diversity in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿1,430.00

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3-Methyl-1H-Pyrazole-5-Carboxylic Acid Ethyl Ester
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory, analgesic, and antipyretic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of pyrazole-containing compounds that are important in medicinal research. Its ester functionality allows for further chemical modifications, making it valuable in optimizing drug candidates during the discovery phase. Also

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory, analgesic, and antipyretic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of pyrazole-containing compounds that are important in medicinal research. Its ester functionality allows for further chemical modifications, making it valuable in optimizing drug candidates during the discovery phase. Also employed in agrochemical research for designing new crop protection agents due to its ability to enhance molecular diversity in synthetic pathways.

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