5-Bromo-N, N-diethylpyrimidin-2-amine

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Reagent Code: #151813
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CAS Number 433684-23-2

science Other reagents with same CAS 433684-23-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.11 g/mol
Formula C₈H₁₂BrN₃
badge Registry Numbers
MDL Number MFCD03646011
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Exhibits utility in agrochemical research for designing novel pesticides with targeted activity. Serves as a building block in medicinal chemistry for modifying pyrimidine-based structures to enhance biological activity and selectivity. Commonly employed in structure-activity relationship (SAR) studies due to its ability to influence binding affinity in drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿510.00
inventory 5g
10-20 days ฿2,310.00
inventory 25g
10-20 days ฿8,050.00

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5-Bromo-N, N-diethylpyrimidin-2-amine
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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. Exhibits utility in agrochemical research for designing novel pesticides with targeted activity. Serves as a building block in medicinal chemistry for modifying pyrimidine-based structures to enhance biological activity and selectivity. Commonly employed in structure-activity relationship (SAR) studies due to its ability to influence binding affinity in drug

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Exhibits utility in agrochemical research for designing novel pesticides with targeted activity. Serves as a building block in medicinal chemistry for modifying pyrimidine-based structures to enhance biological activity and selectivity. Commonly employed in structure-activity relationship (SAR) studies due to its ability to influence binding affinity in drug candidates.

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