N-Benzylidenebenzenesulfonamide

≥98%(HPLC)(N)

Reagent Code: #217512
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CAS Number 13909-34-7

science Other reagents with same CAS 13909-34-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.3 g/mol
Formula C₁₃H₁₁NO₂S
badge Registry Numbers
MDL Number MFCD00011587
thermostat Physical Properties
Melting Point 86°C
inventory_2 Storage & Handling
Storage Room temperature, dryness, inert gas storage

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves as a building block in the development of bioactive molecules, including antimicrobial and anti-inflammatory agents. Its imine functionality allows for further chemical modifications, making it valuable in the synthesis of heterocyclic compounds. Also employed in research settings to study reaction mechanisms involving sulfonamides and Schiff bases.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿700.00
inventory 1g
10-20 days ฿1,130.00
inventory 5g
10-20 days ฿4,060.00

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N-Benzylidenebenzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves as a building block in the development of bioactive molecules, including antimicrobial and anti-inflammatory agents. Its imine functionality allows for further chemical modifications, making it valuable in the synthesis of heterocyclic compounds. Also employed in research settings to study reaction mechanisms involving sulfonamides and Schiff bases.

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves as a building block in the development of bioactive molecules, including antimicrobial and anti-inflammatory agents. Its imine functionality allows for further chemical modifications, making it valuable in the synthesis of heterocyclic compounds. Also employed in research settings to study reaction mechanisms involving sulfonamides and Schiff bases.

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