5-Amino-3-(4-fluorophenyl)pyrazole

≥95%

Reagent Code: #137337
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CAS Number 72411-52-0

science Other reagents with same CAS 72411-52-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.18 g/mol
Formula C₉H₈FN₃
badge Registry Numbers
MDL Number MFCD01023677
thermostat Physical Properties
Melting Point 119-123 °C (lit.)
Boiling Point 435.4±35.0 °C
inventory_2 Storage & Handling
Density 1.334±0.06 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active compounds due to its ability to form hydrogen bonds and participate in π-π stacking interactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies targeting inflammatory and neurological disorders. Also utilized in agrochemical research for designing new pesticides with improved selectivity and efficacy.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,230.00
inventory 5g
10-20 days ฿4,580.00
inventory 25g
10-20 days ฿19,910.00

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5-Amino-3-(4-fluorophenyl)pyrazole
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active compounds due to its ability to form hydrogen bonds and participate in π-π stacking interactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies targeting inflammatory and neurological disorders. Also utilized in agrochemical research for designing ne
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active compounds due to its ability to form hydrogen bonds and participate in π-π stacking interactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies targeting inflammatory and neurological disorders. Also utilized in agrochemical research for designing new pesticides with improved selectivity and efficacy.
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