2,4,6-Trichloro-5-methoxypyrimidine

95%

Reagent Code: #240959
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CAS Number 60703-46-0

science Other reagents with same CAS 60703-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.449 g/mol
Formula C₅H₃Cl₃N₂O
badge Registry Numbers
MDL Number MFCD11226168
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Widely used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective substitution reactions, making it valuable in building complex molecules. Commonly employed in the development of herbicides and fungicides due to the reactivity of the chlorine atoms, which can be displaced by nucleophiles to introduce various functional groups. Also utilized in the preparation of active pharmaceutical ingredients, particularly in the construction of pyrimidine-based drug candidates with biological activity. Its methoxy and chloro substituents provide electronic and steric properties that enhance reaction control during multi-step syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,040.00
inventory 250mg
10-20 days ฿2,070.00
inventory 5g
10-20 days ฿25,440.00
inventory 25g
10-20 days ฿96,000.00
inventory 1g
10-20 days ฿6,080.00
2,4,6-Trichloro-5-methoxypyrimidine
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Widely used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective substitution reactions, making it valuable in building complex molecules. Commonly employed in the development of herbicides and fungicides due to the reactivity of the chlorine atoms, which can be displaced by nucleophiles to introduce various functional groups. Also utilized in the preparation of active pharmaceutical ingredients, particularly in the construction of pyrimidine-based drug candidates with biological activity. Its methoxy and chloro substituents provide electronic and steric properties that enhance reaction control during multi-step syntheses.
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