4-(ethylamino)-2-(methylthio)-5-Pyrimidinemethanol

95%

Reagent Code: #227079
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CAS Number 185040-34-0

science Other reagents with same CAS 185040-34-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.27 g/mol
Formula C₈H₁₃N₃OS
badge Registry Numbers
MDL Number MFCD12911521
thermostat Physical Properties
Melting Point 152-156 °C
Boiling Point 404.7±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.24±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in antiviral and anticancer agents. Its structure supports activity in nucleoside analogs, which interfere with viral replication or tumor cell proliferation. Also employed in agrochemicals as a building block for systemic fungicides. Serves as a reagent in organic synthesis due to reactive hydroxymethyl and amino groups, enabling derivatization for drug discovery research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,390.00
inventory 250mg
10-20 days ฿6,360.00
inventory 1g
10-20 days ฿11,380.00
inventory 5g
10-20 days ฿34,130.00
4-(ethylamino)-2-(methylthio)-5-Pyrimidinemethanol
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Used in the synthesis of pharmaceutical intermediates, particularly in antiviral and anticancer agents. Its structure supports activity in nucleoside analogs, which interfere with viral replication or tumor cell proliferation. Also employed in agrochemicals as a building block for systemic fungicides. Serves as a reagent in organic synthesis due to reactive hydroxymethyl and amino groups, enabling derivatization for drug discovery research.

Used in the synthesis of pharmaceutical intermediates, particularly in antiviral and anticancer agents. Its structure supports activity in nucleoside analogs, which interfere with viral replication or tumor cell proliferation. Also employed in agrochemicals as a building block for systemic fungicides. Serves as a reagent in organic synthesis due to reactive hydroxymethyl and amino groups, enabling derivatization for drug discovery research.

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