4,6-Dichloro-5-(4-fluorophenyl)pyrimidine

95%

Reagent Code: #177404
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CAS Number 146533-37-1

science Other reagents with same CAS 146533-37-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.06 g/mol
Formula C₁₀H₅Cl₂FN₂
badge Registry Numbers
MDL Number MFCD21925697
thermostat Physical Properties
Boiling Point 318.6±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.435±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive chlorine sites, which allow for selective cross-coupling reactions. Commonly employed in research settings for designing novel drug candidates targeting inflammatory diseases and oncology. Also utilized in agrochemical research for developing new herbicides and plant growth regulators. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in final compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,500.00
inventory 250mg
10-20 days ฿11,700.00
inventory 1g
10-20 days ฿39,000.00

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4,6-Dichloro-5-(4-fluorophenyl)pyrimidine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive chlorine sites, which allow for selective cross-coupling reactions. Commonly employed in research settings for designing novel drug candidates targeting inflammatory diseases and oncology. Also utilized in agrochemical research for developing new h

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive chlorine sites, which allow for selective cross-coupling reactions. Commonly employed in research settings for designing novel drug candidates targeting inflammatory diseases and oncology. Also utilized in agrochemical research for developing new herbicides and plant growth regulators. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in final compounds.

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