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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,120.00
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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