Methyl5-(2-bromophenyl)isoxazole-3-carboxylate

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Reagent Code: #213931
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CAS Number 1053657-05-8

science Other reagents with same CAS 1053657-05-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.1 g/mol
Formula C₁₁H₈BrNO₃
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MDL Number MFCD10568325
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its bromophenyl and isoxazole groups make it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex aromatic and heterocyclic systems. Commonly employed in the development of bioactive molecules, including potential anti-inflammatory, antimicrobial, or central nervous system agents. The ester group allows for easy modification, enabling conversion to carboxylic acids, amides, or alcohols for further functionalization in drug discovery pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿10,100.00
Methyl5-(2-bromophenyl)isoxazole-3-carboxylate
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its bromophenyl and isoxazole groups make it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex aromatic and heterocyclic systems. Commonly employed in the development of bioactive molecules, including potential anti-inflammatory, antimicrobial, or central nervous system agents. The ester group allows for easy modification, enabling conversion to carboxylic acids, amides, or alcohols for
Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its bromophenyl and isoxazole groups make it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex aromatic and heterocyclic systems. Commonly employed in the development of bioactive molecules, including potential anti-inflammatory, antimicrobial, or central nervous system agents. The ester group allows for easy modification, enabling conversion to carboxylic acids, amides, or alcohols for further functionalization in drug discovery pathways.
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