N-(2-Methoxybenzylidene)-4-methylbenzenesulfonamide

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Reagent Code: #214742
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CAS Number 100200-70-2

science Other reagents with same CAS 100200-70-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.35 g/mol
Formula C₁₅H₁₅NO₃S
badge Registry Numbers
MDL Number MFCD30579753
thermostat Physical Properties
Boiling Point 456.0±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block for Schiff base compounds, which exhibit biological activities such as antimicrobial, antifungal, and anticancer properties. Its structure allows for easy modification in heterocyclic synthesis, making it valuable in medicinal chemistry research. Also employed in coordination chemistry as a ligand for metal ions, aiding in the study of catalytic reactions and material science applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,850.00
inventory 1g
10-20 days ฿31,440.00

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N-(2-Methoxybenzylidene)-4-methylbenzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block for Schiff base compounds, which exhibit biological activities such as antimicrobial, antifungal, and anticancer properties. Its structure allows for easy modification in heterocyclic synthesis, making it valuable in medicinal chemistry research. Also employed in coordination chemistry as a ligand for metal ions, aiding in the study of catalytic reactions and m

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block for Schiff base compounds, which exhibit biological activities such as antimicrobial, antifungal, and anticancer properties. Its structure allows for easy modification in heterocyclic synthesis, making it valuable in medicinal chemistry research. Also employed in coordination chemistry as a ligand for metal ions, aiding in the study of catalytic reactions and material science applications.

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