Methyl2-(2-chloropyrimidin-4-yl)acetate

95%

Reagent Code: #213449
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CAS Number 1216129-71-3

science Other reagents with same CAS 1216129-71-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.6 g/mol
Formula C₇H₇ClN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure allows for easy functionalization, making it valuable in creating active ingredients that target specific enzymes in plants. Commonly employed in the production of pyrimidine-based compounds with selective biological activity. Also utilized in research for developing new crop protection agents due to its reactivity and stability in multi-step organic transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,000.00
inventory 250mg
10-20 days ฿8,540.00
Methyl2-(2-chloropyrimidin-4-yl)acetate
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure allows for easy functionalization, making it valuable in creating active ingredients that target specific enzymes in plants. Commonly employed in the production of pyrimidine-based compounds with selective biological activity. Also utilized in research for developing new crop protection agents due to its reactivity and stability in multi-s

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure allows for easy functionalization, making it valuable in creating active ingredients that target specific enzymes in plants. Commonly employed in the production of pyrimidine-based compounds with selective biological activity. Also utilized in research for developing new crop protection agents due to its reactivity and stability in multi-step organic transformations.

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