1-Phenyl-3-(trifluoromethyl)-1H-pyrazol-5-amine

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Reagent Code: #226575
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CAS Number 182923-55-3

science Other reagents with same CAS 182923-55-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.19 g/mol
Formula C₁₀H₈F₃N₃
badge Registry Numbers
MDL Number MFCD06738296
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals, contributing to the creation of modern fungicides and pesticides with improved efficacy and environmental profiles. Its trifluoromethyl and amino functional groups enhance binding selectivity and metabolic stability in active compounds. Also employed in research for novel heterocyclic compounds in medicinal chemistry due to its structural versatility.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,250.00
inventory 1g
10-20 days ฿54,600.00
inventory 5g
10-20 days ฿191,060.00

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1-Phenyl-3-(trifluoromethyl)-1H-pyrazol-5-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. It serves as a building block in agrochemicals, contributing to the creation of modern fungicides and pesticides with improved efficacy and environmental profiles. Its trifluoromethyl and amino functional groups enhance binding selectivity and metabolic stability in active compounds. Also employed in research for novel heterocyclic compounds in medicinal chemistry due

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals, contributing to the creation of modern fungicides and pesticides with improved efficacy and environmental profiles. Its trifluoromethyl and amino functional groups enhance binding selectivity and metabolic stability in active compounds. Also employed in research for novel heterocyclic compounds in medicinal chemistry due to its structural versatility.

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