4-(Chloromethyl)-5-methyl-2-(m-tolyl)oxazole

95%

Reagent Code: #156853
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CAS Number 521266-92-2

science Other reagents with same CAS 521266-92-2

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Weight 221.68 g/mol
Formula C₁₂H₁₂ClNO
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MDL Number MFCD09055320
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with oxazole core structures. Its reactive chloromethyl group allows for easy alkylation or attachment to other molecular frameworks, making it valuable in medicinal chemistry for building complex organic compounds. Commonly employed in the preparation of fungicides, herbicides, and kinase inhibitors due to the oxazole ring’s favorable metabolic stability and binding properties. Also utilized in research settings for constructing libraries of heterocyclic compounds in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿630.00
inventory 1g
10-20 days ฿1,670.00

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4-(Chloromethyl)-5-methyl-2-(m-tolyl)oxazole
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with oxazole core structures. Its reactive chloromethyl group allows for easy alkylation or attachment to other molecular frameworks, making it valuable in medicinal chemistry for building complex organic compounds. Commonly employed in the preparation of fungicides, herbicides, and kinase inhibitors due to the oxazole ring’s favorable metabolic stability and binding prope

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with oxazole core structures. Its reactive chloromethyl group allows for easy alkylation or attachment to other molecular frameworks, making it valuable in medicinal chemistry for building complex organic compounds. Commonly employed in the preparation of fungicides, herbicides, and kinase inhibitors due to the oxazole ring’s favorable metabolic stability and binding properties. Also utilized in research settings for constructing libraries of heterocyclic compounds in drug discovery programs.

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