4-[5-(benzylsulfanyl)-4-ethyl-4H-1,2,4-triazol-3-yl]pyridine;4-(5-(Benzylthio)-4-ethyl-4H-1,2,4-triazol-3-yl)pyridine

95%

Reagent Code: #245627
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CAS Number 440638-20-0

science Other reagents with same CAS 440638-20-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.4 g/mol
Formula C₁₆H₁₆N₄S
thermostat Physical Properties
Boiling Point 520.6±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.21±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Exhibits biological activity that supports its role in targeting specific enzymes involved in cell proliferation. Also applied in research settings for designing novel heterocyclic compounds with potential antimicrobial and anti-inflammatory properties. Its structure allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿2,190.00
inventory 5mg
10-20 days ฿8,790.00

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4-[5-(benzylsulfanyl)-4-ethyl-4H-1,2,4-triazol-3-yl]pyridine;4-(5-(Benzylthio)-4-ethyl-4H-1,2,4-triazol-3-yl)pyridine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Exhibits biological activity that supports its role in targeting specific enzymes involved in cell proliferation. Also applied in research settings for designing novel heterocyclic compounds with potential antimicrobial and anti-inflammatory properties. Its structure allows for easy modification, making it valuable in medicinal chemistry for structure-activity r

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Exhibits biological activity that supports its role in targeting specific enzymes involved in cell proliferation. Also applied in research settings for designing novel heterocyclic compounds with potential antimicrobial and anti-inflammatory properties. Its structure allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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