1-Benzyl-1H-pyrazole

95%

Reagent Code: #150442
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CAS Number 10199-67-4

science Other reagents with same CAS 10199-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.20 g/mol
Formula C₁₀H₁₀N₂
badge Registry Numbers
MDL Number MFCD00462231
thermostat Physical Properties
Boiling Point 255-257 °C(Press: 750 Torr)
inventory_2 Storage & Handling
Density 1.078 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex molecules with potential antifungal, anti-inflammatory, or anticancer properties. Commonly employed in research settings for drug discovery and optimization due to the pyrazole ring’s favorable interactions in biological systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,550.00
inventory 250mg
10-20 days ฿2,590.00
inventory 1g
10-20 days ฿5,180.00

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1-Benzyl-1H-pyrazole
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex molecules with potential antifungal, anti-inflammatory, or anticancer properties. Commonly employed in research settings for drug discovery and optimization due to the pyrazole ring’s favorable interactions in biological systems.
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex molecules with potential antifungal, anti-inflammatory, or anticancer properties. Commonly employed in research settings for drug discovery and optimization due to the pyrazole ring’s favorable interactions in biological systems.
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