Allyl-(2,6-dichloro-pyrimidin-4-yl)-carbamic acid tert-butyl ester

95%

Reagent Code: #137832
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CAS Number 1242674-90-3

science Other reagents with same CAS 1242674-90-3

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Weight 304.17 g/mol
Formula C₁₂H₁₅Cl₂N₃O₂
badge Registry Numbers
MDL Number MFCD20227248
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Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and kinase inhibitors. Its structure allows for selective reactivity in coupling reactions, making it valuable in building complex molecules. Commonly employed in research settings for modifying pyrimidine-based compounds to enhance biological activity or stability. Suitable for use in palladium-catalyzed reactions due to the presence of the allyl group, enabling efficient carbon-nitrogen bond formation in drug discovery pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,440.00
inventory 250mg
10-20 days ฿11,500.00
inventory 1g
10-20 days ฿20,900.00

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Allyl-(2,6-dichloro-pyrimidin-4-yl)-carbamic acid tert-butyl ester
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and kinase inhibitors. Its structure allows for selective reactivity in coupling reactions, making it valuable in building complex molecules. Commonly employed in research settings for modifying pyrimidine-based compounds to enhance biological activity or stability. Suitable for use in palladium-catalyzed reactions due to the presence of the allyl group, enabling efficient carbon-n

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and kinase inhibitors. Its structure allows for selective reactivity in coupling reactions, making it valuable in building complex molecules. Commonly employed in research settings for modifying pyrimidine-based compounds to enhance biological activity or stability. Suitable for use in palladium-catalyzed reactions due to the presence of the allyl group, enabling efficient carbon-nitrogen bond formation in drug discovery pathways.

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