2-Chloro-5-(trifluoromethyl)pyrimidine

97%

Reagent Code: #160044
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CAS Number 69034-12-4

science Other reagents with same CAS 69034-12-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.53 g/mol
Formula C₅H₂ClF₃N₂
thermostat Physical Properties
Melting Point 48-52°C
Boiling Point 222°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure allows for easy functionalization, making it valuable in creating active ingredients that target specific biological pathways in pests or pathogens. Also employed in medicinal chemistry for constructing kinase inhibitors and other bioactive molecules due to the electron-deficient pyrimidine ring enhancing binding affinity. Commonly utilized in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or amino groups, enabling rapid diversification in drug discovery programs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,460.00
5g
10-20 days ฿6,400.00
2-Chloro-5-(trifluoromethyl)pyrimidine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure allows for easy functionalization, making it valuable in creating active ingredients that target specific biological pathways in pests or pathogens. Also employed in medicinal chemistry for constructing kinase inhibitors and other bioactive molecules due to the electron-deficient pyrimidine ring enhancing binding affinity. Commonly utilized in cross

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure allows for easy functionalization, making it valuable in creating active ingredients that target specific biological pathways in pests or pathogens. Also employed in medicinal chemistry for constructing kinase inhibitors and other bioactive molecules due to the electron-deficient pyrimidine ring enhancing binding affinity. Commonly utilized in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or amino groups, enabling rapid diversification in drug discovery programs.

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