4-Iodo-1-isopropylpyrazole

98%

Reagent Code: #173413
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CAS Number 313350-82-2

science Other reagents with same CAS 313350-82-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.05 g/mol
Formula C₆H₉IN₂
badge Registry Numbers
MDL Number MFCD11867882
thermostat Physical Properties
Boiling Point 240.3±13.0℃ at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyrazole-based bioactive compounds. Its iodo functionality allows for cross-coupling reactions, enabling the introduction of various substituents through palladium-catalyzed transformations. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds with potential anti-inflammatory, antiviral, or kinase inhibitory activity. Also utilized in research settings to develop novel pesticides due to the pyrazole core’s presence in several crop protection agents.

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Test Parameter Specification
Appearance Colorless to light yellow (Liquid)
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿900.00
inventory 5g
10-20 days ฿3,830.00
inventory 25g
10-20 days ฿15,300.00
inventory 100g
10-20 days ฿55,080.00

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4-Iodo-1-isopropylpyrazole
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyrazole-based bioactive compounds. Its iodo functionality allows for cross-coupling reactions, enabling the introduction of various substituents through palladium-catalyzed transformations. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds with potential anti-inflammatory, antiviral, or kinase inhibitory activity. Also utilized in research settings to develo

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyrazole-based bioactive compounds. Its iodo functionality allows for cross-coupling reactions, enabling the introduction of various substituents through palladium-catalyzed transformations. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds with potential anti-inflammatory, antiviral, or kinase inhibitory activity. Also utilized in research settings to develop novel pesticides due to the pyrazole core’s presence in several crop protection agents.

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