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

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Reagent Code: #184659
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CAS Number 133261-09-3

science Other reagents with same CAS 133261-09-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.27 g/mol
Formula C₁₁H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD08459074
thermostat Physical Properties
Boiling Point 311.5±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.06±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for fungicides and anti-inflammatory agents. Its structure supports the creation of pyrazole-based compounds, which are known for their biological activity. Commonly employed in agrochemical research to design crop protection agents due to its ability to enhance metabolic stability and target specificity. Also utilized in medicinal chemistry for optimizing lead compounds in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,690.00
inventory 250mg
10-20 days ฿37,820.00

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Ethyl 3-isobutyl-1-methyl-1H-pyrazole-5-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for fungicides and anti-inflammatory agents. Its structure supports the creation of pyrazole-based compounds, which are known for their biological activity. Commonly employed in agrochemical research to design crop protection agents due to its ability to enhance metabolic stability and target specificity. Also utilized in medicinal chemistry for optimizing lead compounds in drug discovery

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for fungicides and anti-inflammatory agents. Its structure supports the creation of pyrazole-based compounds, which are known for their biological activity. Commonly employed in agrochemical research to design crop protection agents due to its ability to enhance metabolic stability and target specificity. Also utilized in medicinal chemistry for optimizing lead compounds in drug discovery programs.

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