N'-((3-(4-Fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)benzohydrazide

98%

Reagent Code: #215619
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CAS Number 302938-53-0

science Other reagents with same CAS 302938-53-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 384.41 g/mol
Formula C₂₃H₁₇FN₄O
thermostat Physical Properties
Melting Point 210-212 °C
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and antimicrobial compounds. Its structure supports activity against certain enzyme targets involved in disease pathways, making it valuable in medicinal chemistry research. Also employed in the design of novel hydrazide-based compounds with potential anticancer properties. Commonly utilized in laboratory settings for structure-activity relationship (SAR) studies due to its ability to interact with biological receptors through hydrogen bonding and π-π stacking interactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,060.00
inventory 250mg
10-20 days ฿30,090.00

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N'-((3-(4-Fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)benzohydrazide
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and antimicrobial compounds. Its structure supports activity against certain enzyme targets involved in disease pathways, making it valuable in medicinal chemistry research. Also employed in the design of novel hydrazide-based compounds with potential anticancer properties. Commonly utilized in laboratory settings for structure-activity relationship (SAR) studies due to its ability t

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and antimicrobial compounds. Its structure supports activity against certain enzyme targets involved in disease pathways, making it valuable in medicinal chemistry research. Also employed in the design of novel hydrazide-based compounds with potential anticancer properties. Commonly utilized in laboratory settings for structure-activity relationship (SAR) studies due to its ability to interact with biological receptors through hydrogen bonding and π-π stacking interactions.

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