Ethyl 2-bromooxazole-5-carboxylate

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Reagent Code: #182737
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CAS Number 1060816-22-9

science Other reagents with same CAS 1060816-22-9

blur_circular Chemical Specifications

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Weight 220.02 g/mol
Formula C₆H₆BrNO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and heterocyclic compounds. Its reactive bromine and ester functional groups allow for selective modifications, making it valuable in constructing complex drug scaffolds. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build oxazole-containing derivatives with potential antimicrobial, anti-inflammatory, or anticancer properties. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the oxazole ring’s metabolic stability and favorable electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,400.00
inventory 250mg
10-20 days ฿2,530.00
inventory 1g
10-20 days ฿5,280.00
inventory 25g
10-20 days ฿80,000.00
inventory 5g
10-20 days ฿22,400.00
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Ethyl 2-bromooxazole-5-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and heterocyclic compounds. Its reactive bromine and ester functional groups allow for selective modifications, making it valuable in constructing complex drug scaffolds. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build oxazole-containing derivatives with potential antimicrobial, anti-inflammatory, or anticancer properties. Also utilized in agroch

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and heterocyclic compounds. Its reactive bromine and ester functional groups allow for selective modifications, making it valuable in constructing complex drug scaffolds. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build oxazole-containing derivatives with potential antimicrobial, anti-inflammatory, or anticancer properties. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the oxazole ring’s metabolic stability and favorable electronic properties.

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