N2,N2-Dimethylpyrimidine-2,5-diamine

95%

Reagent Code: #217343
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CAS Number 56621-99-9

science Other reagents with same CAS 56621-99-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.17 g/mol
Formula C₆H₁₀N₄
badge Registry Numbers
MDL Number MFCD11656641
inventory_2 Storage & Handling
Storage 2-8°C

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 medicinal chemistry due to its ability to form hydrogen bonds and interact with biological targets. Also employed in the preparation of agrochemicals and functional materials where nitrogen-rich heterocyclic frameworks enhance performance. Its dimethylamino groups improve solubility and binding affinity, making it valuable in optimizing drug candidates during lead modification.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,030.00
inventory 250mg
10-20 days ฿3,120.00
inventory 5g
10-20 days ฿38,300.00
inventory 1g
10-20 days ฿8,590.00
N2,N2-Dimethylpyrimidine-2,5-diamine
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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 medicinal chemistry due to its ability to form hydrogen bonds and interact with biological targets. Also employed in the preparation of agrochemicals and functional materials where nitrogen-rich heterocyclic frameworks enhance performance. Its dimethylamino groups improve solubility and binding affinity, making it valuable in

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 medicinal chemistry due to its ability to form hydrogen bonds and interact with biological targets. Also employed in the preparation of agrochemicals and functional materials where nitrogen-rich heterocyclic frameworks enhance performance. Its dimethylamino groups improve solubility and binding affinity, making it valuable in optimizing drug candidates during lead modification.

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