Ethyl 5-(tert-butyl)-1H-pyrazole-3-carboxylate

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Reagent Code: #184353
label
Alias 5-(tert-butyl)-2H-pyrazole-3-carboxylate
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CAS Number 83405-70-3

science Other reagents with same CAS 83405-70-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.25 g/mol
Formula C₁₀H₁₆N₂O₂
badge Registry Numbers
MDL Number MFCD00173782
thermostat Physical Properties
Melting Point 141-144 °C
Boiling Point 322.3 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential anti-inflammatory and analgesic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives that are of interest in medicinal research. Its ester functionality allows for further chemical modifications, making it valuable in optimizing drug candidates during lead optimization stages. Also employed in agrochemical research for designing new active ingredients in crop protection agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,970.00
inventory 10g
10-20 days ฿3,680.00
inventory 25g
10-20 days ฿8,880.00
inventory 100g
10-20 days ฿32,110.00

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Ethyl 5-(tert-butyl)-1H-pyrazole-3-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential anti-inflammatory and analgesic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives that are of interest in medicinal research. Its ester functionality allows for further chemical modifications, making it valuable in optimizing drug candidates during lead optimization stages. Also employed in agrochemi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential anti-inflammatory and analgesic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives that are of interest in medicinal research. Its ester functionality allows for further chemical modifications, making it valuable in optimizing drug candidates during lead optimization stages. Also employed in agrochemical research for designing new active ingredients in crop protection agents.

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