Methyl 3-(2-nitrophenyl)-1H-pyrazole-5-carboxylate

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Reagent Code: #208657
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CAS Number 57446-04-5

science Other reagents with same CAS 57446-04-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.21 g/mol
Formula C₁₁H₉N₃O₄
badge Registry Numbers
MDL Number MFCD22628335
thermostat Physical Properties
Boiling Point 483.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential anti-inflammatory and anticancer properties. Its structure supports further functionalization for use in medicinal chemistry research. Also employed in agrochemical research for designing new crop protection agents due to its aromatic and heterocyclic features that enhance molecular interaction with biological targets.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿470.00
inventory 1g
10-20 days ฿1,450.00
inventory 5g
10-20 days ฿5,750.00

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Methyl 3-(2-nitrophenyl)-1H-pyrazole-5-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential anti-inflammatory and anticancer properties. Its structure supports further functionalization for use in medicinal chemistry research. Also employed in agrochemical research for designing new crop protection agents due to its aromatic and heterocyclic features that enhance molecular interaction with biological targets.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential anti-inflammatory and anticancer properties. Its structure supports further functionalization for use in medicinal chemistry research. Also employed in agrochemical research for designing new crop protection agents due to its aromatic and heterocyclic features that enhance molecular interaction with biological targets.

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