1-Methyl-1H-pyrazole-4-thiol

≥95%

Reagent Code: #203781
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CAS Number 1152556-14-3

science Other reagents with same CAS 1152556-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 114.1688 g/mol
Formula C₄H₆N₂S
badge Registry Numbers
MDL Number MFCD11193919
thermostat Physical Properties
Boiling Point 206.3±13.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.25±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antidiabetic agents. It serves as a building block in agrochemicals for creating herbicides and fungicides due to its ability to enhance bioactivity. The thiol group allows for easy functionalization, enabling the formation of disulfide or sulfide derivatives in drug design. Also employed in coordination chemistry as a ligand for metal complexes with potential catalytic or biological activity.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿16,000.00
inventory 50mg
10-20 days ฿25,600.00
inventory 100mg
10-20 days ฿48,000.00

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1-Methyl-1H-pyrazole-4-thiol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antidiabetic agents. It serves as a building block in agrochemicals for creating herbicides and fungicides due to its ability to enhance bioactivity. The thiol group allows for easy functionalization, enabling the formation of disulfide or sulfide derivatives in drug design. Also employed in coordination chemistry as a ligand for metal complexes with potential catalytic or biological a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antidiabetic agents. It serves as a building block in agrochemicals for creating herbicides and fungicides due to its ability to enhance bioactivity. The thiol group allows for easy functionalization, enabling the formation of disulfide or sulfide derivatives in drug design. Also employed in coordination chemistry as a ligand for metal complexes with potential catalytic or biological activity.

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