1-(1-Isopropyl-1H-pyrazol-4-yl)-ethylamine

97%

Reagent Code: #201149
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CAS Number 1007459-53-1

science Other reagents with same CAS 1007459-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.23 g/mol
Formula C₈H₁₅N₃
badge Registry Numbers
MDL Number MFCD08700769
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical synthesis as a key intermediate for developing biologically active compounds, particularly in the production of kinase inhibitors and central nervous system agents. Its structure supports binding to enzyme active sites, making it valuable in drug discovery for oncology and neurological disorders. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,400.00

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1-(1-Isopropyl-1H-pyrazol-4-yl)-ethylamine
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Used in pharmaceutical synthesis as a key intermediate for developing biologically active compounds, particularly in the production of kinase inhibitors and central nervous system agents. Its structure supports binding to enzyme active sites, making it valuable in drug discovery for oncology and neurological disorders. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies

Used in pharmaceutical synthesis as a key intermediate for developing biologically active compounds, particularly in the production of kinase inhibitors and central nervous system agents. Its structure supports binding to enzyme active sites, making it valuable in drug discovery for oncology and neurological disorders. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds.

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