Ethyl 3-methyl-1H-pyrazole-5-carboxylate

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Reagent Code: #182151
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CAS Number 4027-57-0

science Other reagents with same CAS 4027-57-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.17 g/mol
Formula C₇H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD00052514
thermostat Physical Properties
Melting Point 80-84°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. Its structure supports the construction of pyrazole-based heterocycles, which are common motifs in medicinal chemistry due to their metabolic stability and ability to engage in hydrogen bonding. It is also employed in agrochemical research for designing new pesticides and herbicides, leveraging its reactivity in cross-coupling and cyclization reactions. Additionally, it serves as a building block in the preparation of functional materials and specialty chemicals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿460.00
inventory 25g
10-20 days ฿1,580.00
inventory 100g
10-20 days ฿6,260.00
inventory 1g
10-20 days ฿148.50
inventory 500g
10-20 days ฿31,260.00

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Ethyl 3-methyl-1H-pyrazole-5-carboxylate
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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 other bioactive compounds. Its structure supports the construction of pyrazole-based heterocycles, which are common motifs in medicinal chemistry due to their metabolic stability and ability to engage in hydrogen bonding. It is also employed in agrochemical research for designing new pesticides and herbicides, leveraging its reactivity in cross-coupling and

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive compounds. Its structure supports the construction of pyrazole-based heterocycles, which are common motifs in medicinal chemistry due to their metabolic stability and ability to engage in hydrogen bonding. It is also employed in agrochemical research for designing new pesticides and herbicides, leveraging its reactivity in cross-coupling and cyclization reactions. Additionally, it serves as a building block in the preparation of functional materials and specialty chemicals.

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