4-Chloro-6-(methylthio)pyrimidine

97%

Reagent Code: #160098
fingerprint
CAS Number 89283-48-7

science Other reagents with same CAS 89283-48-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.63 g/mol
Formula C₅H₅ClN₂S
thermostat Physical Properties
Melting Point 50-51°C
Boiling Point 260.2±25.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its reactive chlorine and methylthio groups that allow further functionalization. Commonly employed in the production of sulfonylurea herbicides, where it serves as a building block for constructing the pyrimidine ring system. Also utilized in pharmaceutical research for developing kinase inhibitors and other bioactive molecules. Its versatility in cross-coupling reactions makes it valuable in medicinal chemistry for creating diverse compound libraries.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,200.00
5g
10-20 days ฿4,380.00
10g
10-20 days ฿6,710.00
25g
10-20 days ฿15,430.00
4-Chloro-6-(methylthio)pyrimidine
No image available

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its reactive chlorine and methylthio groups that allow further functionalization. Commonly employed in the production of sulfonylurea herbicides, where it serves as a building block for constructing the pyrimidine ring system. Also utilized in pharmaceutical research for developing kinase inhibitors and other bioactive molecules. Its versatility in cross-coupling reactions makes it valuable in m

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its reactive chlorine and methylthio groups that allow further functionalization. Commonly employed in the production of sulfonylurea herbicides, where it serves as a building block for constructing the pyrimidine ring system. Also utilized in pharmaceutical research for developing kinase inhibitors and other bioactive molecules. Its versatility in cross-coupling reactions makes it valuable in medicinal chemistry for creating diverse compound libraries.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...