Ethyl 4-chloro-6-methylpyrimidine-5-carboxylate

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Reagent Code: #184452
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CAS Number 157981-60-7

science Other reagents with same CAS 157981-60-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.62 g/mol
Formula C₈H₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD25959552
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key 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 building complex pyrimidine-based molecules. It is also employed in research settings for the preparation of kinase inhibitors and other biologically active compounds. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the reactivity of the ester and chloro groups.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,890.00
inventory 250mg
10-20 days ฿7,320.00
inventory 1g
10-20 days ฿11,990.00

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Ethyl 4-chloro-6-methylpyrimidine-5-carboxylate
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Used as a key 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 building complex pyrimidine-based molecules. It is also employed in research settings for the preparation of kinase inhibitors and other biologically active compounds. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the reactivity

Used as a key 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 building complex pyrimidine-based molecules. It is also employed in research settings for the preparation of kinase inhibitors and other biologically active compounds. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the reactivity of the ester and chloro groups.

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