2-(Trifluoromethyl)pyrimidin-5-ol

98%

Reagent Code: #240410
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CAS Number 100991-09-1

science Other reagents with same CAS 100991-09-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.09 g/mol
Formula C₅H₃F₃N₂O
badge Registry Numbers
MDL Number MFCD10696944
thermostat Physical Properties
Boiling Point 140.9±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.521±0.06 g/cm3(Predicted)
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the creation of bioactive molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for modifying drug candidates to improve metabolic stability and binding affinity. Also utilized in agrochemicals for designing new pesticides, such as fungicides, due to the electron-withdrawing nature of the trifluoromethyl group, which enhances compound durability and activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,280.00
250mg
10-20 days ฿2,240.00
1g
10-20 days ฿6,400.00
5g
10-20 days ฿19,200.00
25g
10-20 days ฿64,000.00
2-(Trifluoromethyl)pyrimidin-5-ol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the creation of bioactive molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for modifying drug candidates to improve metabolic stability and binding affinity. Also utilized in agrochemicals for designing new pesticides, such as fungicides, due to the electron-withdrawing nature of the trifluor

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the creation of bioactive molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for modifying drug candidates to improve metabolic stability and binding affinity. Also utilized in agrochemicals for designing new pesticides, such as fungicides, due to the electron-withdrawing nature of the trifluoromethyl group, which enhances compound durability and activity.

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