Methyl 3-ethyl-1H-pyrazole-5-carboxylate

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Reagent Code: #207065
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CAS Number 834869-10-2

science Other reagents with same CAS 834869-10-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.17 g/mol
Formula C₇H₁₀N₂O₂
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 and analgesic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives that are valuable in medicinal research. Its ester functionality allows for easy modification, making it useful in structure-activity relationship (SAR) studies during drug discovery. Additionally, it finds application in agrochemical research for designing new crop protection agents due to the biological activity associated with pyrazole scaffolds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,120.00
inventory 1g
10-20 days ฿5,870.00

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Methyl 3-ethyl-1H-pyrazole-5-carboxylate
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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 and analgesic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives that are valuable in medicinal research. Its ester functionality allows for easy modification, making it useful in structure-activity relationship (SAR) studies during drug discovery. Additionally, it find

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory and analgesic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives that are valuable in medicinal research. Its ester functionality allows for easy modification, making it useful in structure-activity relationship (SAR) studies during drug discovery. Additionally, it finds application in agrochemical research for designing new crop protection agents due to the biological activity associated with pyrazole scaffolds.

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