2-Chloro-N-(5-methylisoxazol-3-yl)acetamide

95%

Reagent Code: #215715
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CAS Number 59826-53-8

science Other reagents with same CAS 59826-53-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.59 g/mol
Formula C₆H₇ClN₂O₂
badge Registry Numbers
MDL Number MFCD03001122
thermostat Physical Properties
Melting Point 62 °C(Solv: methanol (67-56-1))
Boiling Point 378.2±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.383±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of sulfonamide antibiotics, particularly in the production of sulfamethoxazole. It plays a critical role in forming the amide bond that links the sulfonamide group to the isoxazole ring, enhancing the antimicrobial activity of the final compound. Commonly employed in pharmaceutical manufacturing for antibacterial agents effective against a broad spectrum of pathogens. Its reactivity and stability make it suitable for use in controlled industrial environments where precise reaction conditions are maintained.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,990.00
inventory 1g
10-20 days ฿10,740.00
inventory 5g
10-20 days ฿37,610.00

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2-Chloro-N-(5-methylisoxazol-3-yl)acetamide
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Used as a key intermediate in the synthesis of sulfonamide antibiotics, particularly in the production of sulfamethoxazole. It plays a critical role in forming the amide bond that links the sulfonamide group to the isoxazole ring, enhancing the antimicrobial activity of the final compound. Commonly employed in pharmaceutical manufacturing for antibacterial agents effective against a broad spectrum of pathogens. Its reactivity and stability make it suitable for use in controlled industrial environments wh

Used as a key intermediate in the synthesis of sulfonamide antibiotics, particularly in the production of sulfamethoxazole. It plays a critical role in forming the amide bond that links the sulfonamide group to the isoxazole ring, enhancing the antimicrobial activity of the final compound. Commonly employed in pharmaceutical manufacturing for antibacterial agents effective against a broad spectrum of pathogens. Its reactivity and stability make it suitable for use in controlled industrial environments where precise reaction conditions are maintained.

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