3-(Methylthio)-1H-pyrazol-5-amine

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Reagent Code: #210188
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CAS Number 117736-74-0

science Other reagents with same CAS 117736-74-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 129.18 g/mol
Formula C₄H₇N₃S
badge Registry Numbers
MDL Number MFCD18642411
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and selectivity in drug candidates. Also utilized in agrochemical research for designing new pesticides and herbicides, where the methylthio and amino groups contribute to improved stability and biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,550.00
inventory 250mg
10-20 days ฿18,410.00
inventory 1g
10-20 days ฿46,150.00

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3-(Methylthio)-1H-pyrazol-5-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and selectivity in drug candidates. Also utilized in agrochemical research for designing new pesticides

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and selectivity in drug candidates. Also utilized in agrochemical research for designing new pesticides and herbicides, where the methylthio and amino groups contribute to improved stability and biological activity.

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