N-(4-Chloro-3-(trifluoromethyl)phenyl)-3-oxobutanamide

≥98%

Reagent Code: #218567
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CAS Number 392721-37-8

science Other reagents with same CAS 392721-37-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.6429 g/mol
Formula C₁₁H₉ClF₃NO₂
badge Registry Numbers
MDL Number MFCD01001285
thermostat Physical Properties
Melting Point 141.7 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and antimicrobial agents. Its structure supports the formation of heterocyclic rings, which are common in bioactive molecules. It is also employed in agrochemical research for designing herbicides and fungicides due to the presence of chlorine and trifluoromethyl groups that enhance biological activity and stability. The compound’s ketone and amide functionalities allow for further chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿2,190.00
inventory 25mg
10-20 days ฿7,430.00
inventory 50mg
10-20 days ฿12,240.00
inventory 100mg
10-20 days ฿21,230.00

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N-(4-Chloro-3-(trifluoromethyl)phenyl)-3-oxobutanamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and antimicrobial agents. Its structure supports the formation of heterocyclic rings, which are common in bioactive molecules. It is also employed in agrochemical research for designing herbicides and fungicides due to the presence of chlorine and trifluoromethyl groups that enhance biological activity and stability. The compound’s ketone and amide functionalities allow for further c

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and antimicrobial agents. Its structure supports the formation of heterocyclic rings, which are common in bioactive molecules. It is also employed in agrochemical research for designing herbicides and fungicides due to the presence of chlorine and trifluoromethyl groups that enhance biological activity and stability. The compound’s ketone and amide functionalities allow for further chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.

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