5-Neopentyl-1H-pyrazol-3-amine

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Reagent Code: #214767
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CAS Number 377079-77-1

science Other reagents with same CAS 377079-77-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.2242 g/mol
Formula C₈H₁₅N₃
badge Registry Numbers
MDL Number MFCD18809351
thermostat Physical Properties
Boiling Point 316.8±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.052±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for strong binding interactions with specific enzyme active sites, enhancing selectivity and potency. Also employed in agrochemical research for designing novel pesticides with improved metabolic stability. The amine and pyrazole functionalities enable easy derivatization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,320.00
inventory 500mg
10-20 days ฿6,390.00

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5-Neopentyl-1H-pyrazol-3-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. Its structure allows for strong binding interactions with specific enzyme active sites, enhancing selectivity and potency. Also employed in agrochemical research for designing novel pesticides with improved metabolic stability. The amine and pyrazole functionalities enable easy derivatization, making it valuable in medicinal chemistry for structure-activity r

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for strong binding interactions with specific enzyme active sites, enhancing selectivity and potency. Also employed in agrochemical research for designing novel pesticides with improved metabolic stability. The amine and pyrazole functionalities enable easy derivatization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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