4,6-Dichloro-2,5-diphenylpyrimidine

98%

Reagent Code: #174025
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CAS Number 29133-99-1

science Other reagents with same CAS 29133-99-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.17 g/mol
Formula C₁₆H₁₀Cl₂N₂
badge Registry Numbers
MDL Number MFCD00209572
thermostat Physical Properties
Melting Point 130-133 °C(lit.)
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 for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its reactive chlorine atoms, which allow for further functionalization through cross-coupling reactions. Commonly employed in research settings for the design of novel pyrimidine-based drugs with potential antiviral and anti-inflammatory properties. Its structural features make it valuable in medicinal chemistry for optimizing drug candidates targeting specific enzyme pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿670.00
inventory 1g
10-20 days ฿2,480.00
inventory 5g
10-20 days ฿8,110.00

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4,6-Dichloro-2,5-diphenylpyrimidine
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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 the preparation of bioactive molecules due to its reactive chlorine atoms, which allow for further functionalization through cross-coupling reactions. Commonly employed in research settings for the design of novel pyrimidine-based drugs with potential antiviral and anti-inflammatory properties. Its structural features make it valuable

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 the preparation of bioactive molecules due to its reactive chlorine atoms, which allow for further functionalization through cross-coupling reactions. Commonly employed in research settings for the design of novel pyrimidine-based drugs with potential antiviral and anti-inflammatory properties. Its structural features make it valuable in medicinal chemistry for optimizing drug candidates targeting specific enzyme pathways.

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