tert-Butyl 4-(5-bromo-6-methylpyridin-2-yl)piperazine-1-carboxylate

95%

Reagent Code: #152281
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CAS Number 1289040-88-5

science Other reagents with same CAS 1289040-88-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.26 g/mol
Formula C₁₅H₂₂BrN₃O₂
badge Registry Numbers
MDL Number MFCD29113123
thermostat Physical Properties
Boiling Point 450.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.341±0.06 g/cm3(Predicted)
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure, featuring a pyridine ring and piperazine moiety, allows for selective modification, making it valuable in creating potent bioactive molecules. Commonly employed in medicinal chemistry research to build more complex drug candidates targeting specific signaling pathways. Also utilized in the preparation of pyridine-based derivatives with potential neurological and anti-inflammatory activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,920.00
inventory 250mg
10-20 days ฿11,760.00
inventory 1g
10-20 days ฿34,380.00

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tert-Butyl 4-(5-bromo-6-methylpyridin-2-yl)piperazine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure, featuring a pyridine ring and piperazine moiety, allows for selective modification, making it valuable in creating potent bioactive molecules. Commonly employed in medicinal chemistry research to build more complex drug candidates targeting specific signaling pathways. Also utilized in the preparation of pyridine-based derivatives with potential n

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure, featuring a pyridine ring and piperazine moiety, allows for selective modification, making it valuable in creating potent bioactive molecules. Commonly employed in medicinal chemistry research to build more complex drug candidates targeting specific signaling pathways. Also utilized in the preparation of pyridine-based derivatives with potential neurological and anti-inflammatory activity.

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