5-Aminopyridine-2-carbothioamide

95%

Reagent Code: #131905
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CAS Number 1347815-39-7

science Other reagents with same CAS 1347815-39-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.2 g/mol
Formula C₆H₇N₃S
badge Registry Numbers
MDL Number MFCD20265328
thermostat Physical Properties
Boiling Point 389.7±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.373±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 heterocyclic compounds, particularly in the development of pharmaceuticals with antimicrobial and antiviral properties. It serves as a building block for pyridine-based drug candidates due to its ability to form stable complexes with metal ions, which is beneficial in medicinal chemistry. Also employed in the preparation of thiourea derivatives that show potential in cancer research and enzyme inhibition studies. Its reactivity makes it valuable in organic synthesis for constructing nitrogen- and sulfur-containing rings.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,400.00
inventory 250mg
10-20 days ฿7,500.00
inventory 1g
10-20 days ฿20,250.00

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5-Aminopyridine-2-carbothioamide
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Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the development of pharmaceuticals with antimicrobial and antiviral properties. It serves as a building block for pyridine-based drug candidates due to its ability to form stable complexes with metal ions, which is beneficial in medicinal chemistry. Also employed in the preparation of thiourea derivatives that show potential in cancer research and enzyme inhibition studies. Its reactivity makes it valuable in organic s

Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the development of pharmaceuticals with antimicrobial and antiviral properties. It serves as a building block for pyridine-based drug candidates due to its ability to form stable complexes with metal ions, which is beneficial in medicinal chemistry. Also employed in the preparation of thiourea derivatives that show potential in cancer research and enzyme inhibition studies. Its reactivity makes it valuable in organic synthesis for constructing nitrogen- and sulfur-containing rings.

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