4,6-Dimethoxy-2-(methylthio)pyrimidine

98%

Reagent Code: #177801
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CAS Number 90905-46-7

science Other reagents with same CAS 90905-46-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.23 g/mol
Formula C₇H₁₀N₂O₂S
badge Registry Numbers
MDL Number MFCD00792663
thermostat Physical Properties
Melting Point 56-60 °C at N/A mmHg
Boiling Point 312.7 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. Its structure allows for functional modifications that enhance biological activity in crop protection agents. Also employed in research for developing novel kinase inhibitors due to the pyrimidine core’s affinity for enzyme binding sites. Commonly utilized in cross-coupling reactions to introduce methylthio and methoxy groups in heterocyclic compounds for drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿450.00
inventory 5g
10-20 days ฿1,520.00
inventory 25g
10-20 days ฿5,300.00

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4,6-Dimethoxy-2-(methylthio)pyrimidine
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. Its structure allows for functional modifications that enhance biological activity in crop protection agents. Also employed in research for developing novel kinase inhibitors due to the pyrimidine core’s affinity for enzyme binding sites. Commonly utilized in cross-coupling reactions to introduce methylthio and methoxy groups in heterocyclic compounds

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. Its structure allows for functional modifications that enhance biological activity in crop protection agents. Also employed in research for developing novel kinase inhibitors due to the pyrimidine core’s affinity for enzyme binding sites. Commonly utilized in cross-coupling reactions to introduce methylthio and methoxy groups in heterocyclic compounds for drug discovery.

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