N-(2,4-Dimethoxybenzylidene)-4-methylbenzenesulfonamide

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Reagent Code: #214899
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CAS Number 314248-25-4

science Other reagents with same CAS 314248-25-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.38 g/mol
Formula C₁₆H₁₇NO₄S
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MDL Number MFCD00589468
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based compounds with potential biological activity. It serves as a building block in the development of pharmaceuticals, leveraging the sulfonamide group's prevalence in drug molecules for its favorable pharmacokinetic properties. Commonly employed in condensation reactions to form imine derivatives that can be further modified for medicinal chemistry research. Also utilized in the study of crystallography and molecular structure due to its stable Schiff base formation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,670.00
inventory 250mg
10-20 days ฿18,140.00
inventory 1g
10-20 days ฿48,960.00

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N-(2,4-Dimethoxybenzylidene)-4-methylbenzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based compounds with potential biological activity. It serves as a building block in the development of pharmaceuticals, leveraging the sulfonamide group's prevalence in drug molecules for its favorable pharmacokinetic properties. Commonly employed in condensation reactions to form imine derivatives that can be further modified for medicinal chemistry research. Also utilized in the study of crystallography and mo

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based compounds with potential biological activity. It serves as a building block in the development of pharmaceuticals, leveraging the sulfonamide group's prevalence in drug molecules for its favorable pharmacokinetic properties. Commonly employed in condensation reactions to form imine derivatives that can be further modified for medicinal chemistry research. Also utilized in the study of crystallography and molecular structure due to its stable Schiff base formation.

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