3-Chloro-4-fluoro-N-[4-[[2-(phenylcarbonyl)hydrazino]carbonyl]benzyl]benzenesulfonamide

99%

Reagent Code: #80323
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CAS Number 852918-02-6

science Other reagents with same CAS 852918-02-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 461.89 g/mol
Formula C₂₁H₁₇ClFN₃O₄S
badge Registry Numbers
MDL Number MFCD06683895
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting enzyme inhibition. Its structure suggests potential applications in the design of sulfonamide-based drugs, which are often explored for their antibacterial, anti-inflammatory, or anticancer properties. Researchers utilize this chemical to study its interactions with specific protein targets, aiding in the development of novel therapeutic agents. Additionally, its unique functional groups make it a valuable candidate for further chemical modifications to optimize pharmacological activity and selectivity.

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Test Parameter Specification
Appearance white to beige powder
Purity 98.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,880.00
inventory 250mg
10-20 days ฿21,450.00

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3-Chloro-4-fluoro-N-[4-[[2-(phenylcarbonyl)hydrazino]carbonyl]benzyl]benzenesulfonamide
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This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting enzyme inhibition. Its structure suggests potential applications in the design of sulfonamide-based drugs, which are often explored for their antibacterial, anti-inflammatory, or anticancer properties. Researchers utilize this chemical to study its interactions with specific protein targets, aiding in the development of novel therapeutic agents. Additionally, its unique functional groups make it a valuable candidate for further chemical modifications to optimize pharmacological activity and selectivity.
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