6-Chloro-2-methoxypyrimidin-4-amine

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Reagent Code: #160487
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CAS Number 3286-55-3

science Other reagents with same CAS 3286-55-3

blur_circular Chemical Specifications

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Weight 159.57 g/mol
Formula C₅H₆ClN₃O
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 ability to enhance selectivity and efficacy in crop protection agents. Its structure supports binding to specific enzyme sites in pests or unwanted plants, making it valuable in developing systemic and residual control products. Also explored in pharmaceutical research for potential kinase inhibitor applications, where the chloro and methoxy groups contribute to targeted molecular interactions. Commonly employed in cross-coupling reactions to build more complex heterocyclic systems in drug discovery and crop science.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,600.00
inventory 5g
10-20 days ฿12,640.00
inventory 10g
10-20 days ฿25,080.00

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6-Chloro-2-methoxypyrimidin-4-amine
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance selectivity and efficacy in crop protection agents. Its structure supports binding to specific enzyme sites in pests or unwanted plants, making it valuable in developing systemic and residual control products. Also explored in pharmaceutical research for potential kinase inhibitor applications, where the chloro and methoxy groups contribute to targeted molecular interactio

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance selectivity and efficacy in crop protection agents. Its structure supports binding to specific enzyme sites in pests or unwanted plants, making it valuable in developing systemic and residual control products. Also explored in pharmaceutical research for potential kinase inhibitor applications, where the chloro and methoxy groups contribute to targeted molecular interactions. Commonly employed in cross-coupling reactions to build more complex heterocyclic systems in drug discovery and crop science.

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