1-(tert-Butyl)-3-cyclopropyl-1H-pyrazol-5-amine

95%

Reagent Code: #151011
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CAS Number 187795-43-3

science Other reagents with same CAS 187795-43-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.26 g/mol
Formula C₁₀H₁₇N₃
badge Registry Numbers
MDL Number MFCD00122781
thermostat Physical Properties
Boiling Point 315.1±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.18±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof storage, inert atmosphere

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 enhance binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of biologically active molecules targeting inflammatory diseases and neurological disorders. Its cyclopropyl and tert-butyl groups contribute to improved lipophilicity and steric hindrance, which are beneficial for optimizing drug potency and pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,220.00
inventory 250mg
10-20 days ฿7,110.00
inventory 1g
10-20 days ฿17,090.00

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1-(tert-Butyl)-3-cyclopropyl-1H-pyrazol-5-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. It serves as a building block in medicinal chemistry due to its ability to enhance binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of biologically active molecules targeting inflammatory diseases and neurological disorders. Its cyclopropyl and tert-butyl groups contribute to improved lipophilicity and steri

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 enhance binding selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of biologically active molecules targeting inflammatory diseases and neurological disorders. Its cyclopropyl and tert-butyl groups contribute to improved lipophilicity and steric hindrance, which are beneficial for optimizing drug potency and pharmacokinetic properties.

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