3-Phenylisoxazole-5-carbonyl chloride

97%

Reagent Code: #228270
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CAS Number 124953-60-2

science Other reagents with same CAS 124953-60-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.61 g/mol
Formula C₁₀H₆ClNO₂
badge Registry Numbers
MDL Number MFCD09817542
thermostat Physical Properties
Melting Point 90.5-91.5 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive acid chloride group allows it to form amide or ester linkages, making it valuable in constructing bioactive molecules. Commonly employed in the development of fungicides and herbicides due to the stability and biological activity of the isoxazole ring. Also utilized in medicinal chemistry for building blocks in kinase inhibitors and anti-inflammatory agents. Its phenyl and heterocyclic structure enhances binding affinity in drug design, enabling optimization of pharmacokinetic properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿6,900.00
3-Phenylisoxazole-5-carbonyl chloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive acid chloride group allows it to form amide or ester linkages, making it valuable in constructing bioactive molecules. Commonly employed in the development of fungicides and herbicides due to the stability and biological activity of the isoxazole ring. Also utilized in medicinal chemistry for building blocks in kinase inhibitors and anti-inflammatory agents. Its phenyl and heterocyclic structure enhances

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive acid chloride group allows it to form amide or ester linkages, making it valuable in constructing bioactive molecules. Commonly employed in the development of fungicides and herbicides due to the stability and biological activity of the isoxazole ring. Also utilized in medicinal chemistry for building blocks in kinase inhibitors and anti-inflammatory agents. Its phenyl and heterocyclic structure enhances binding affinity in drug design, enabling optimization of pharmacokinetic properties.

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