4-Hydroxy-2-(trifluoromethyl)pyrimidine

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Reagent Code: #194983
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CAS Number 1546-80-1

science Other reagents with same CAS 1546-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.09 g/mol
Formula C₅H₃F₃N₂O
badge Registry Numbers
MDL Number MFCD00151833
thermostat Physical Properties
Melting Point 168-171°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports binding to enzyme active sites, making it valuable in drug design. Also employed in agrochemicals for creating herbicides and fungicides due to its stability and reactivity. The presence of both hydroxyl and trifluoromethyl groups enhances its utility in forming hydrogen bonds and improving metabolic stability in active compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,030.00
inventory 250mg
10-20 days ฿1,520.00
inventory 5g
10-20 days ฿16,930.00

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4-Hydroxy-2-(trifluoromethyl)pyrimidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports binding to enzyme active sites, making it valuable in drug design. Also employed in agrochemicals for creating herbicides and fungicides due to its stability and reactivity. The presence of both hydroxyl and trifluoromethyl groups enhances its utility in forming hydrogen bonds and improving metabolic stability in active compounds.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports binding to enzyme active sites, making it valuable in drug design. Also employed in agrochemicals for creating herbicides and fungicides due to its stability and reactivity. The presence of both hydroxyl and trifluoromethyl groups enhances its utility in forming hydrogen bonds and improving metabolic stability in active compounds.

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