2-Chloro-4-ethoxy-pyrimidine

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Reagent Code: #164223
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CAS Number 83774-09-8

science Other reagents with same CAS 83774-09-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.586 g/mol
Formula C₆H₇ClN₂O
badge Registry Numbers
MDL Number MFCD00234199
thermostat Physical Properties
Melting Point 35 °C
Boiling Point 279 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.235 g/cm3
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its reactive chlorine and electron-deficient pyrimidine ring. Its ethoxy group enhances lipophilicity, improving membrane permeability in active ingredients. Also employed in pharmaceutical research for developing kinase inhibitors and other bioactive molecules. Commonly utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to introduce aryl or amino substituents in drug discovery programs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,140.00
inventory 250mg
10-20 days ฿8,530.00
inventory 1g
10-20 days ฿19,530.00
inventory 5g
10-20 days ฿73,980.00

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2-Chloro-4-ethoxy-pyrimidine
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its reactive chlorine and electron-deficient pyrimidine ring. Its ethoxy group enhances lipophilicity, improving membrane permeability in active ingredients. Also employed in pharmaceutical research for developing kinase inhibitors and other bioactive molecules. Commonly utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to introduce aryl or amino substituents in drug disc

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its reactive chlorine and electron-deficient pyrimidine ring. Its ethoxy group enhances lipophilicity, improving membrane permeability in active ingredients. Also employed in pharmaceutical research for developing kinase inhibitors and other bioactive molecules. Commonly utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to introduce aryl or amino substituents in drug discovery programs.

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