5-(trifluoromethyl)-1H-Pyrazol-3-amine

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Reagent Code: #195788
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CAS Number 852443-61-9

science Other reagents with same CAS 852443-61-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.0899 g/mol
Formula C₄H₄F₃N₃
badge Registry Numbers
MDL Number MFCD06738292
thermostat Physical Properties
Melting Point 90-92 °C
Boiling Point 289.984 °C at 760mmHg
inventory_2 Storage & Handling
Density 1.561 g/cm3
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing drug efficacy. Also employed in agrochemicals to improve the stability and activity of crop protection agents. The trifluoromethyl group contributes to increased metabolic stability and lipophilicity, making it valuable in optimizing pharmacokinetic properties of active compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿560.00
inventory 1g
10-20 days ฿1,400.00
inventory 5g
10-20 days ฿6,960.00
inventory 25g
10-20 days ฿34,750.00

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5-(trifluoromethyl)-1H-Pyrazol-3-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing drug efficacy. Also employed in agrochemicals to improve the stability and activity of crop protection agents. The trifluoromethyl group contributes to increased metabolic stability and lipophilicity, making it valuable in optimizing pharmacokinetic properties of active compounds.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing drug efficacy. Also employed in agrochemicals to improve the stability and activity of crop protection agents. The trifluoromethyl group contributes to increased metabolic stability and lipophilicity, making it valuable in optimizing pharmacokinetic properties of active compounds.

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